CN1232443A - 新的对三联苯化合物 - Google Patents
新的对三联苯化合物 Download PDFInfo
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- CN1232443A CN1232443A CN97198341A CN97198341A CN1232443A CN 1232443 A CN1232443 A CN 1232443A CN 97198341 A CN97198341 A CN 97198341A CN 97198341 A CN97198341 A CN 97198341A CN 1232443 A CN1232443 A CN 1232443A
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
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- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
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- C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
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- C07C217/20—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted by halogen atoms, by trihalomethyl, nitro or nitroso groups, or by singly-bound oxygen atoms
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- C07C233/25—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
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- C07C233/27—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
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- C07C233/80—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
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Abstract
本发明在从成熟B细胞分化成产生抗体细胞到产生抗体的过程中,提供含有抑制IgE产生,且不抑制或微弱抑制同时产生的IgG、IgM和/或IgA产生的物质的选择性的IgE产生抑制剂及用式(Ⅰ)表示的化合物、其制备方法、含有它们的医药。式中,R1~R13是氢、卤素、低级烷基、低级烷氧基等、X是-O-、-CH2-、-NR14-或-S(O)p-、Y是低级烷基或低级烯基等。
Description
技术领域
本发明涉及新的对三联苯化合物及其制备方法、IgE产生的选择性抑制剂、免疫抑制剂及抗过敏剂。
背景技术
近年,进行过的很多组织、脏器等移植手术中存在的严重课题是手术后的移植部分产生排斥的排异反应。避免这些,对于成功地进行移植手术是非常重要的。
开发、应用了硫唑嘌呤、类皮质激素、环孢菌素,藤霉素等各种免疫抑制剂,用于对于脏器或组织移植的排异反应、因骨髓移植引起的宿主对移植物反应的预防及治疗上。可是,这些药物在效果和副作用上还不能得到满足。
另一方面,近年,特应性皮炎、过敏性鼻炎、支气管哮喘、过敏性结膜炎等的过敏性疾病与有世界性范围增加的趋势,而成为大的问题。以往的抗过敏剂是来自肥大细胞的游离化学介质的抑制剂、游离了的化学介质的受体抑制剂或过敏性炎症反应的抑制剂等,但它们中的任何一种都是对症治疗方法,而不能成为根本的过敏性疾病的治疗药。
作为根本的过敏性疾病的治疗药,可考虑与过敏性疾病的发生有很大关系的IgE抗体产生抑制剂。
作为具有IgE产生抑制作用的化合物之一的物质,有Suplatast甲苯磺酸盐(IPD-1151-T)。报告中叙述了该物质与2型的T细胞(Th2细胞)作用,通过抑制IL-4产生,可抑制B细胞向产生IgE抗体细胞的分化(Jpn.Pharmacol.(1993)61,31-39)。
直接与B细胞作用,抑制产生IgE抗体的化合物,例如有作为肥大细胞脱颗粒抑制剂的DSCG(咽泰)或萘多罗米钠。报告中叙述了它们阻碍B细胞的类别转换(J.Exp.Med.(1994)180:663-671、J.Allergy Clin.Immunol.(1996)97:1141-1150)。另外,在J.Med.Chem.(1997)40:395-407中也叙述了与B细胞直接作用,抑制IgE产生的化合物。
免疫球蛋白对于防御感染是必要的,由于抑制IgE抗体以外的免疫球蛋白不理想,所以希望开发IgE选择性高的强力抑制剂。
对于具有抗炎症作用的物质,在特开昭60-13730、J.Med.Chem.(1996)39:1846-1856、WO96/10012中叙述了具有邻三苯骨架的化合物、在特公昭43-19935、特开昭62-294650及WO96/18606中叙述了具有联苯基骨架的化合物。
另外,在化学和药品公报(Chemical & PharmaceuticalBulletin,24(4),613-620(1976))、抗生素杂志(The Journalof Antibiotics,32(6),559-564(1979))及农业生物化学(Agricultural Biological Chemistry,49(3),867-868(1985))等叙述了具有对三联苯骨架的化合物,但对于免疫抑制作用及抗过敏性作用完全没有叙述。
发明的公开
本发明的目的在于提供具有优良的选择性的IgE产生抑制作用、免疫抑制作用和/或抗过敏性作用的选择性的IgE产生抑制剂、免疫抑制剂和/或抗过敏性剂。另外,在于提供具有这种作用的新的化合物及其制备方法。
本发明提供从成熟B细胞分化成产生抗体细胞到产生抗体的过程中,含有抑制IgE产生,且不抑制或微弱抑制同时产生的IgG、IgM和/或IgA的免疫球蛋白产生的物质的选择性的IgE产生抑制剂、免疫抑制剂和/或抗过敏性剂。进而,提供选择性的IgE产生抑制方法、抑制免疫反应的方法或治疗过敏性疾病的方法和/或预防的方法,其特征是给药该物质。作为另一个方案,为制备选择性的IgE产生抑制剂、抑制免疫反应或治疗和/或预防过敏性疾病的医药,提供使用该物质。
进而,本发明作为具有上述作用的物质的一个例子,提供用式(I)表示的化合物、其药学上可接受的盐、其水合物或前体药物,〔式中,R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、也可具有取代基的低级烷基磺酰氧基、也可具有取代基的低级烷基亚硫酰基、硝基、氰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基、也可具有取代基的氨磺酰基或也可具有取代基的杂环、X是-O-、-CH2-、-NR14-(其中,R14是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或乙酰基)或-S(O)p-(其中,p是0~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,Y是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基。另外,R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R11、R12及R13、R11及-X-Y或R13及-X-Y,也可一起形成含有1个以上的O、S或NR15(其中,R15是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或也可具有取代基的芳基磺酰基)的,可具有取代基的5~6元环。但是,除去R6、R7、R8及R9中,1个以上是卤素,其它的是氢;R6、R7、R8及R9都是卤素;及R2~R13都是氢,卤素或氰基中的任何1种的情况。另外,R6、R7、R8及R9同时都是氢时,R1不是氢、氟、也可具有取代基的低级烷基及也可具有取代基的低级烷氧基或R2、R3、R4、R5及R12都是氢或者R13不是氢及卤素。进而,R6、R7、R8或R9中至少1个是氢以外的基时,R1不是甲基及乙酰氧基、或R13不是氢、也可具有取代基的低级烷氧羰基及也可具有取代基的氨基甲酰基或者-X-Y不是甲氧基、另外,除去用式(I′)表示的化合物,(式中,R1′是氢或羟基、R13′是羟基或甲氧基)〕。
另外,本发明提供化合物(I),其药学上可接受的盐、其水合物或其前体药物的医药、详细地说,提供选择性的IgE产生抑制剂、免疫抑制剂或抗过敏性剂。
进而,本发明提供用式(I″)表示的化合物、其药学上可接受的盐、它们的水合物或含有它们的前体药物的选择性的IgE产生抑制剂、免疫抑制剂和/或抗过敏性剂。〔式中,R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、也可具有取代基的低级烷基磺酰氧基、也可具有取代基的低级烷基亚硫酰基、硝基、氰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基、也可具有取代基的氨磺酰基或也可具有取代基的杂环、X是-O-、-CH2-、-NR14-(其中,R14是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或乙酰基)或-S(O)p-(其中,p是0~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,Y是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基。另外,R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R12、R12及R13、R11及-X-Y或R13及-X-Y,也可成为一起地形成含有1个以上的O、S或NR15(其中,R15是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或也可具有取代基的芳基磺酰基)的,也可具有取代基的5~6元环。但是,除去用式(I′)表示的化合物,(式中,R1′是氢或烃基、R13′是羟基或甲氧基)〕。
进而,提供选择性的IgE产生抑制方法、抑制免疫反应的方法或治疗过敏性疾病的方法或预防的方法,其特征是给与化合物(I)或(I″)。进而,作为另一个方案,为制备选择性的IgE产生抑制剂、抑制免疫反应、治疗或预防过敏性疾病的医药,提供了化合物(I)或(I″)的应用。
进而,作为又一个方案,本发明提供了用式(I_)、上述式(I)或上述式(I′)表示的化合物、其药学上可接受的盐或其水合物的制备方法,〔式中,R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、也可具有取代基的低级烷基磺酰氧基、也可具有取代基的低级烷基亚硫酰基、硝基、氰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基、也可具有取代基的氨磺酰基或也可具有取代基的杂环、X是-O-、-CH2-、-NR14-(其中,R14是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或乙酰基)或-S(O)p-(其中,p是0~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,Y是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基。另外,R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R11、R12及R13、R11及-X-Y或R13及-X-Y,一起地形成含有1个以上的O、S或NR15(其中,R15是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或也可具有取代基的芳基磺酰基)的,可具有取代基的5~6元环。但是,除去R6、R7、R8及R9中,1个以上是卤素,其它的是氢;R6、R7、R8及R9都是卤素;及R2~R13都是氢,卤素或氰基中的任何一种的情况。另外,R6、R7、R8及R9同时都是氢时,R1不是氢、氟、也可具有取代基的低级烷基及也可具有取代基的低级烷氧基或R2、R3、R4、R5及R12都是氢、或者R13不是氢及卤素。进而,R6、R7、R8或R9中至少1个是氢以外的基时,R1不是甲基或者乙酰氧基、或R13不是氢、也可具有取代基的低级烷氧羰基及也可具有取代基的氨基甲酰基或者-X-Y不是甲氧基。〕其特征是使用式(II):表示的化合物和用式(III):(式(II)及式(III)中,R1~R13、X及Y与上述式(I)时定义相同、A及Z的一方是二羟基硼烷、二低级烷氧基硼烷、二低级烷基硼烷、或
另一方是卤素或-OSO2(CqF2q+1)(其中,q是0~4的整数))表示的化合物进行反应,或用式(II′):表示的化合物和用式(III′):(式(II′)及式(III′)中,R1~R13、X及Y与上述式(I)时定义相同、A及Z与上述式(II)及(III)时定义相同)表示的化合物进行反应。进而,作为另一个方法,提供了用上述式(III′)、上述式(I)或上述式(I′)表示的化合物、其药学上可接受的盐或它们的水合物的制备方法,其特征是将用式(IV):表示的化合物及用式(V):(式(IV)及(V)中,R1~R9、与上述式(I)的定义相同、Z1与上述式(II)的Z定义相同,A1及A2分别独立地与上述式(III)的A定义相同。但是,A1是具有比A2高的反应性或具有相同反应性的基)表示的化合物进行反应,接着,将用式(VI):(式中,R10~R13、X、Y与上述式(I)时定义相同、Z2与上述式(II)的Z定义相同)表示的化合物进行反应以及用上述式(I_)、上述式(I)或上述式(I′)表示的化合物、其药学上可接受的盐或者它们的水合物的制备方法,其特征是将用式(IV′):(式中,R6~R9与用上述式(I)表示时定义相同、A1及A2分别独立地与上述式(III)的A定义相同。但是,A2是具有比A1高的反应性或具有相同反应性的基)表示的化合物和用上述式(VI)表示的化合物进行反应、接着,将用上述式(V)表示的化合物进行反应。
附图简述
图1是表示本发明化合物(I-839)在人的外周血淋巴细胞的抗体产生抑制效果图。纵轴表示将不存在化合物下的产生抗体量作为100%的抗体量,横轴表示化合物浓度。
图2是表示化合物No.36在人的外周血淋巴细胞的抗体产生抑制效果图。纵轴表示将不存在化合物下的产生抗体量作为100%的抗体量,横轴表示化合物浓度。
图3是表示本发明的化合物(I-967)在小白鼠脾脏淋巴细胞的抗体产生抑制效果图。纵轴表示将不存在化合物下的产生抗体量作为100%的抗体量,横轴表示化合物浓度。
图4是表示本发明化合物(I-963)对于由于小白鼠的抗原刺激引起的肺组织洗涤液中的炎症性细胞浸润抑制效果图。纵轴是炎症性细胞数、横轴分别表示总炎症性细胞数、巨噬细胞数、嗜酸性白细胞数、嗜中性白细胞数。白柱是吸入生理食盐水代替卵白蛋白的试验组、黑柱是吸入抗原、引起炎症反应、不给与本发明化合物试验组、灰柱是吸入抗原、引起炎症反应、给与本发明化合物试验组。
实施发明的最佳方案
在本说明书中,“卤素”是指氟、氯、溴及碘。特别优选的是氟及氯。“卤代低级烷基”、“卤代低级烯基”、“卤代芳基”中的卤素也与上述定义相同。
“低级烷基”是指碳数1~10、优选的是碳数1~8、更优选的是碳数1~6、最优选的是碳数1~4的直链或支链的烷基,例如包括甲基、乙基、正丙基、异丙基、正丁基、异丁基、仲丁基、叔丁基、正戊基、异戊基、新戊基、己基、异己基、正庚基、异庚基、正辛基、异辛基、正壬基、正癸基等。
作为R1~R13、R14及R15的“也可具有取代基的低级烷基”的取代基,可举出卤素、羟基、也可用低级烷氧基取代的低级烷氧基、羧基、低级烷氧基羰基或酰氧基等、也可用1个以上的这些取代基取代任意的位置。
作为Y的“也可具有取代基的低级烷基”的取代基,可举出卤素、羟基、羧基、低级烷氧基羰基,也可用低级烷氧基取代的低级烷氧基、酰基、酰氧基、羟基或也可用低级烷基取代的氨基、羟基、低级烷氧基、羧基低级烷氧基、芳基低级烷氧基或也可用杂环取代的亚氨基、氨基甲酰基或也可用低级烷氧基羰基取代的腙基、也可用低级烷基取代的环烷基、也可用低级烷基取代的环烯基、氰基、也可用低级烷基或氨基取代的氨基甲酰基、也可用低级烷基取代的硫代氨基甲酰基、
(其中,A环是环烷基或杂环)、低级烷基、卤代低级烷基、羧基低级烷基、低级烷氧羰基低级烷基、卤素、羟基、低级烷氧基、羧基、低级烷氧羰基、低级烯氧基羰基、酰氧基、硝基、氰基、氨基、低级烷氧基羰基氨基、酰基氨基、低级烷基磺酰氨基、低级烷基氨基或也可用胍基取代的芳基、也可用杂环取代的低级烷基、卤素、羟基、羧基、低级烷氧基羰基、低级烷基磺酰基、低级烷基芳基磺酰基、巯基、低级烷基硫基或也可用芳基取代的杂环等。
“卤代低级烷基”、“羟基低级烷基”、“羧基低级烷基”、“低级烷氧基羰基低级烷基”、“低级烷基硫基”、“低级烷基氨基”、“低级烷基磺酰基”、“低级烷基磺酰氧基”、“低级烷基磺酰氨基”、“低级烷基亚硫酰基”、“低级烷基芳基”、“低级烷基芳基磺酰基”、“二低级烷基氨基甲酰基”、“二低级烷基硼烷”、“低级烷氧基”、“羧基低级烷氧基”、“芳基低级烷氧基”、“低级烷氧基低级烷氧基”、“低级烷氧基芳基”、“二低级烷氧基硼烷”的烷基部分与上述“低级烷基”相同,作为“也可具有取代基”的取代基,可举出卤素、羟基、低级烷氧基、羧基、低级烷氧基羰基、酰基氧基、环烷基、也可用低级烷基取代的芳基,或杂环等。在任意的位置上也可以有1个以上的这些取代基。
“低级烷氧羰基”的低级烷基部分与上述“低级烷基”相同、“也可具有取代基的低级烷氧羰基”的取代基与“也可具有取代基的低级烷氧基”的取代基相同。
“低级烷氧基羰基低级烷基”、“低级烷氧基羰基低级烯基”、“低级烷氧基羰基氨基”的“低级烷氧基羰基”部分与上述“低级烷氧基羰基”相同。
“低级烯基”是指碳数2~10、优选的是碳数2~8、最优选的是碳数3~6的直链或支链的烯基。具体地说,包括乙烯基、丙烯基、异丙烯基、丁烯基、异丁烯基、丁二烯基、戊烯基、异戊烯基、戊二烯基、己烯基、异己烯基、己二烯基、庚烯基、辛烯基、壬烯基、癸烯基等、在任意的位置上有1个以上的双键。“也可具有取代基的低级烯基”的取代基与上述“也可具有取代基的低级烷氧基”的取代基相同。
“低级烷氧基羰基低级烯基”、“卤代低级烯基”、“低级烯氧基”、“低级烯氧基羰基”、“低级烯基氨基”的低级烯基部分与上述“低级烯基”相同。
“也可具有取代基的低级烯氧基”的取代基与上述“也可具有取代基的低级烷氧基”的取代基相同。
“低级炔基”是指碳数2~10、优选的是碳数2~8、最优选的是碳数3~8的直链或支链的炔基、具体地说,包括乙炔基、丙炔基、丁炔基、戊炔基、己炔基、庚炔基、辛炔基、壬炔基、癸炔基等。它们是在任意的位置上具有1个以上的三键、进而,也可具有双键。“也可具有取代基的低级炔基”的取代基与上述“也可具有取代基的低级烷氧基”的取代基相同。
“酰基”是指碳数1~10、优选的是碳数1~8、更优选的是碳数1~6、最优选的是碳数1~4的链状或碳数3~8、优选的是碳数3~6的环状脂肪族酰基及芳酰基。具体地说,包括甲酰基、乙酰基、丙酰基、丁酰基、异丁酰基、戊酰基、新戊酰基、己酰基、丙烯酰基、丙炔酰基、甲基丙烯酰基及丁烯酰基、环己烷羰基、苯甲酰基等。“也可具有取代基的低级酰基”的取代基与上述“也可具有取代基的低级烷氧基”的取代基相同,进而,芳酰基作为取代基也可具有低级烷基。
“酰氧基”、“酰氨基”的酰基部分与“酰基”相同、“也可具有取代基的酰氧基”的取代基也与“也可具有取代基的酰基”相同。
“环烷基”是碳数3~6的碳环、例如包括环丙基、环丁基、环戊基、环己基等。作为“也可具有取代基的环烷基”的取代基,可举出低级烷基、卤素、羟基、羧基、低级烷氧基羰基、低级烷氧基、芳基、杂环等、也可取代1个以上的任意位置。
“环烯基”是指在上述环烷基的环中任意位置上具有1个以上的双键、具体地说,包括环丙烯基、环丁烯基、环戊烯基、环己烯基、环己二烯基等。“也可具有取代基的环烯基”的取代基与上述“环烷基”的取代基相同。
“也可具有取代基的氨基”包括取代氨基及非取代氨基,作为取代基,例如可举出也可用低级烷基芳基等取代的低级烷基、也可用卤素取代的低级烯基、低级烷基磺酰基、低级烷基芳基磺酰基、低级烷氧基羰基、氨磺酰基、也可用卤素取代的酰基或氨基甲酰基等。
“也可具有取代基的氨基甲酰基”包括取代氨基甲酰基及非取代氨基甲酰基、作为取代基,可举出低级烷基、低级烷基磺酰基、氨磺酰基、也可用卤素取代的酰基或氨基等。
“也可具有取代基的氨磺酰基”包括取代氨磺酰基及非取代氨磺酰基、作为它的取代基,可举出也可用芳基取代的低级烷基、或低级烯基等。
“芳基”包括苯基、萘基、蒽基、茚基、菲基等。作为“也可具有取代基的芳基”的取代基可举出也可用卤素或羧基取代的低级烷基、羟基、卤素、低级烷氧基、低级酰氧基、羧基、低级烷氧基羰基、低级烯氧基羰基、也可用低级烷基、低级烷基磺酰基、低级烷氧基羰基或酰基取代的氨基、胍基、硝基、芳基或杂环等、可用这些取代基取代1个以上的任意位置。
“低级烷基芳基”、“卤代芳基”、“低级烷氧基芳基”、“芳基磺酰基”、“芳基低级烷氧基”、“低级烷基芳基磺酰基”、“芳基取代杂环”、“芳酰基”、“芳酰氧基”的芳基部分,与上述“芳基”相同、“也可具有取代基”的取代基部分也与上述“也可具有取代基的芳基”的取代基相同。
“杂环”是指在环内具有1个以上的从O、S及N任意选择性的杂环原子的杂环、具体地说,包括吡咯基、咪唑基、吡唑基、吡啶基、哒嗪基、嘧啶基、吡嗪基、三唑基、三嗪基、异噁唑基、噁唑基、噁二唑基、异噻唑基、噻唑基、噻二唑基、呋喃基及噻吩基等5~6元芳香族杂环和、吲哚基、咔唑基、吖啶基、苯并咪唑基、吲唑基、吲哚嗪基、喹啉基、异喹啉基、噌啉基、酞嗪基、喹唑啉基、萘啶基、喹喔啉基、嘌呤基、喋啶基、苯并异噁唑基、苯并噁唑基、苯并二噁唑基、苯并异噻唑基、苯并噻唑基、苯并噻二唑基、苯并呋喃基、苯并噻吩基、苯并三唑基等稠合芳香族杂环、二噁唑基、环硫基、环氧基、环氧硫基、吖叮啶基、噻吩基、吡咯烷基、吡咯啉基、咪唑烷基、咪唑啉基、吡唑烷基、吡唑啉基、哌啶基、哌嗪基、吗啉基等脂环式杂环。作为“也可具有取代基的杂环”的取代基,可举出低级烷基、低级烯基、羟基、卤素、羧基、低级烷氧基羰基、低级烷氧基、巯基、低级烷硫基、低级烷基磺酰基、芳基或杂环等,也可取代1个以上的任意位置。“芳基取代杂环”的杂环部分也与上述“杂环”相同。
“也可含有1个以上的O、S或NR15、也可具有取代基的5~6元环”是指R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R11、R12及R13、R11及-X-Y或R13及-X-Y和其各取代基结合的构成苯基的2个碳原子成为一起地形成的5~6元环。作为其具体例,可举出上述的各取代基成为一起地形成-(CH2)3-、-(CH2)4-、-O(CH2)mO-、-O(CH2)n-、-(CH2)nO-、
S(CH2)mS-、-S(CH2)n-、-(CH2)nS-、-NR15(CH2)mNR15-、-NR13(CH2)n-、-(CH2)nNR15-、-O(CH2)mS-、-S(CH2)mO-、-S(CH2)mNR15-、-NR15(CH2)mS-、-O(CH2)mNR15-、-NR15(CH2)mO-、-O-CH=CH-、-CH=CH-O-、-S-CH=CH-、-CH=CH-S-、-NR15-CH=CH-、-CH=CH-NR15、-S-CH=N-、-N=CH-S-、-S-N=CH-、-CH=N-S-、-O-CH=N-、-N=CH-O-、-O-N=CH-、-CH=N-O-、-NR15-CH=N-、-N=CH-NR15-、-NR15-N=CH-、-CH=N-NR15-、-N=CH-CH=CH-、-CH=CH-CH=N-、-N=N-CH=CH-、-CH=CH-N=N-、-N=CH-N=CH-、-CH=N-CH=N-、-N=CH-CH=N-(m是1或2、n是2或3)等、与构成苯基的2个碳原子一起地形成5~6元环。作为这些环上的取代基是也可具有1个以上的羟基、卤素,也可用低级烷氧羰基或杂环取代的低级烷基、也可用卤素取代的低级烯基、或也可用卤素取代的低级亚烷基等。对于“也可含有1个以上的O或NR15、也可具有取代基的5~6元环”、“含有1个以上的O或NR15、也可具有取代基的5~6元环”及“含有1个以上的O、也可具有取代基的5~6元环”中的取代基,只要没有特别说明,也是相同的。
“低级亚烷基”是指碳数1~6、优选的是碳数1~4、最优选的是碳数1~3的直链或支链状的亚烷基、例如包括亚甲基、亚乙基、异亚丙基、亚乙烯基、次甲基等。
“R2~R13全部是氢、卤素或氰基中的任何一种时”例如是指R2~R13相同或不同地是氢、卤素或氰基。例如包括R2~R13全是氢、全是卤素、R2~R13中任何1个是卤素,其余是氢、任何1个是氰基、基余是卤素、任何一个是氰基、其余是氢、任何一个是卤素、任何一个是氰基、其余是氢等。
对于所说的“化合物(I)”、“化合物(I″)”、或“化合物(I_)”,也包括可生成的各种化合物在药学上可接受的盐。作为“药学上可接受的盐”例如可举出盐酸、硫酸、硝酸、磷酸、氢氟酸、氢溴酸等的无机酸盐;甲酸、醋酸、酒石酸、乳酸、柠檬酸、富马酸、马来酸、琥珀酸等的有机酸盐;铵、三甲基铵、三乙基铵等有机碱的盐;钠、钾等的碱金属盐或钙、镁等的碱土类金属的盐类。
本发明的化合物,包括其水合物及全部的立体异构体(例如被限旋光异构体)。
进而,本发明的化合物包括其药物前体。“药物前体”是指在生物体内容易变换成具有活性的化合物(I)或(I″)的化合物群。可用常法进行药物前体化。作为一般的药物前体化,可举出将羟基置换成可取代的酰氧基(其中,取代基是羧基、磺基、氨基或低级烷基氨基)或膦酰氧基等。优选的是只要将取代在R1上的烃基置换成-OCOCH2CH2COOH、-OCOCH=CHCOOH、-OCOCH2SO3H、-OPO3H2、-OCOCH2NMe2、-OCO-Pyr(Pyr表示吡啶)等。
在本说明书中,“化合物(I)”是除去化合物(I′)的新的化合物群、“化合物(I″)”是包括化合物(I)及公知化合物的化合物群、“化合物(I_)”是包括化合物(I)及化合物(I′)的化合物群。
化合物(I)及(I″)具有完全选择性的IgE产生抑制活性、抑制免疫作用和/或抗过敏性作用,但其中特别优选的是以下化合物。
在式(I)及(I″)中,1)、R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基或也可具有取代基的氨磺酰基、X是-O-、-CH2-、-NR14-(其中,R14是氢或也可具有取代基的低级烷基)或-S(O)p-(其中,p是0~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基或也可具有取代基的环烯基、R1及R4、R1及R2、R8及R9、R11及-X-Y或R13及-X-Y,一起地形成含有1个以上的O或NR15的,具有取代基的5~6元环的化合物、2)、R1是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、低级烷基磺酰基、甲酰基、也可具有取代基的氨基、低级烷基亚硫酰基、酰氧基、硝基、氰基、也可具有取代基的氨磺酰基或杂环、R2是氢、羟基、卤素、也可具有取代基的低级烷基或也可具有取代基的低级烷基磺酰氧基、R3是氢、羟基、卤素或也可具有取代基的低级烷氧基、R4是氢、也可具有取代基的低级烷基、卤素、也可具有取代基的低级烷氧基、硝基或也可具有取代基的氨基、R5是氢、也可具有取代基的低级烷氧基、低级烷氧羰基或羧基、R6是氢、卤素、也可具有取代基的低级烷基、羧基、低级烷氧羰基、硝基、甲酰基、氨基或低级烷基磺酰氧基、R7及R8分别独立地是氢、卤素、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、甲酰基或也可具有取代基的氨基。R9是氢、羟基、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、也可具有取代基的氨基甲酰基或也可具有取代基的氨基、R10是氢或低级烷氧基、R11是氢、卤素、也可具有取代基的低级烷基、羧基、低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、硝基或氨基、R12是氢、R13是羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰氧基、甲酰基、硝基或也可具有取代基的氨基、进而,在式(I″)中,R13也可以是氢、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烯基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基、R1及R2、R1及R4、R8及R9、R11及-X-Y或R13及-X-Y,一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、3)、R1是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、低级烷基磺酰基、甲酰基、也可具有取代基的氨基、低级烷基亚硫酰基、酰氧基、硝基、氰基、也可具有取代基的氨磺酰基或杂环(以下,R1简称为R1-1)或R2或R4一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、优选的是R1是氢、羟基、卤素、可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基或也可具有取代基的低级烷基磺酰氧基、也可具有取代基的氨基、也可具有取代基的氨磺酰基(以下,R1简称为R1-2)或R2或R4一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、进而,更优选的,R1是氢、羟基、卤素、低级烷氧基低级烷氧基、芳基低级烷氧基、低级烯氧基、低级烷基磺酰氧基、氨基、低级烷基氨基或低级烯基氨基(以下,R1简称为R1-3)或者R2或R4一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、特别优选的,R1是氢、羟基、氯、氟、甲氧基甲氧基、苄氧基、3-甲基-2-丁酰氧基、甲磺酰氧基、氨基、二甲氨基或3-甲基-2-丁酰氨基(以下,R1简称为R1-4)或者R2或R4一起地形成-OCH2O-或-CH=CH-NH-的化合物、4)、R2是氢、羟基、卤素、低级烷基或也可具有取代基的低级烷基磺酰氧基(以下,R2简称为R2-1)或与R1一起形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、优选的是R2是氢、卤素或碳数是1~3的低级烷基(以下,R2简称为R2-2)的化合物、5)、R3是氢、羟基、卤素或也可具有取代基的低级烷氧基(以下,R3简称为R3-1)的化合物、优选的是R3是氢或卤素(以下,R3简称为R3-2)的化合物、最优选的是R3是氢或氟(以下,R3简称为R3-3)的化合物、6)、R4是氢、也可具有取代基的低级烷基、卤素、也可具有取代基的低级烷氧基、硝基或也可具有取代基的氨基(以下,R4简称为R4-1)或与R1一起形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、优选的是R4是氢、低级烷基、低级烷氧基或卤素(以下,R4简称为R4-2)或与R1一起形成-OCH2O-的化合物、7)、R5是氢、也可具有取代基的低级烷氧基、低级烷氧羰基或羧基(以下,R5简称为R5-1)的化合物、优选的是R5是氢、低级烷氧羰基或羧基(以下,R5简称为R5-2)的化合物、最优选的是R5是氢(以下,R5简称为R5-3)的化合物,8)、R6是氢、卤素、也可具有取代基的低级烷基、羧基、低级烷氧羰基、硝基、甲酰基、氨基或低级烷基磺酰氧基(以下,R6简称为R6-1)的化合物、优选的是R6是氢、低级烷基或卤素(以下,R6简称为R6-2)的化合物、最优选的是R6是氢、碳数1~3的烷基或卤素(以下,R6简称为R6-3)的化合物、9)、R7是氢、卤素、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、甲酰基或也可具有取代基的氨基(以下,R7简称为R7-1)的化合物、优选的是R7是氢、低级烷基或低级烷氧基(以下,R7简称为R7-2)的化合物、10)、R8是氢、卤素、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、甲酰基或也可具有取代基的氨基(以下,R8简称为R8-1)或与R9一起地形成含有1个以上的O的,可具有取代基的5~6元环的化合物、优选的是R8是氢、低级烷基或低级烷氧基(以下,R8简称为R8-2)的化合物、11)、R9是氢、羟基、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、也可具有取代基的氨基甲酰基、或也可具有取代基的氨基(以下,R9简称为R9-1)或与R8一起地形成含有1个以上的O的,可具有取代基的5~6元环的化合物、优选的是R9是氢、羟基、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、也可具有取代基的氨基甲酰基、或也可具有取代基的氨基(以下,R9简称为R9-2)的化合物、最优选的是R9是氢、羟基、低级烷基、羟基低级烷基、低级烷氧基羰基低级烯基、低级烷氧基低级烷氧基、低级烷基磺酰氧基、二低级烷基氨基甲酰基、羧基、低级烷氧基羰基或氨基(以下,R9简称为R9-3)的化合物、最优选的是R9是氢、羟基、甲基、羟基甲基、乙氧基羰基乙烯基、甲氧基甲氧基、甲磺酰基、二甲基氨基甲酰基、羧基、甲氧基羰基或氨基(以下,R9简称为R9-4)的化合物、12)、R10是氢或低级烷氧基(以下,R10简称为R10-1)的化合物、优选的是R10是氢(以下,R10简称为R10-2)的化合物、13)、R11是氢、卤素、也可具有取代基的低级烷基、羧基、低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、硝基或氨基(以下,R11简称为R11-1)或与-X-Y一起形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基(低级烯基、卤代低级烯基等)的5~6元环的化合物、优选的是R11是氢或卤素(以下,R11简称为R11-2)的化合物、14)、R12是氢的化合物、15)、R13是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰氧基、甲酰基、硝基或也可具有取代基的氨基(以下,R13简称为R13-1)或与-X-Y一起地形成含有O或NR15(其中,R15与上述情况定义相同)的,可具有取代基(低级烯基、卤代低级烯基等)的5~6元环的化合物、优选的是R13是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰氧基、甲酰基或也可具有取代基的氨基(以下,R13简称为R13-2)的化合物、最优选的是R13是羟基、卤素、也可用羟基或卤素取代的低级烷基、也可用低级烷氧基羰基或低级烷氧基取代的低级烷氧基、也可用卤素取代基的低级烯氧基、芳酰氧基、低级烷基磺酰氧基、甲酰基或氨基(以下,R13简称为R13-3)的化合物、最优选R13是羟基、氟、甲基、羟甲基、甲基碘、甲氧基、乙氧基、异丙氧基、乙氧基、羰基甲氧基、甲氧基甲氧基、氯丁酰氧基、溴丙烯氧基、氯丙烯氧基、溴丁烯氧基、二氯丙烯氧基、乙氧基羰基、苯酰氧基、甲磺酰氧基、甲酰基或氨基(以下,R13简称为R13-4)的化合物、16)、X是-O-、-NR14-或-S(O)p-(其中,p是0~2的整数)(以下,X简称为X1)或与R13及Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、优选的是X是-O-、-NH-、-NMe-或-SO2-(以下,X简称为X2)的化合物、更优选的是X是-O-、-NH-或-NMe-(以下,X简称为X3)的化合物、最优选的是X是-O-的化合物、17)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的环烯基、低级烷基磺酰基、也可具有取代基的芳基磺酰基、低级烷氧基羰基或也可具有取代基的酰基(以下,Y简称为Y1)或与R13及X一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、优选的是Y是可具有以下取代基的低级烷基、〔卤素;羟基;也可用低级烷基取代的氨基;低级烷氧基;羧基;低级烷氧基羰基;酰基;环烷基;环烯基;氰基;羟基;也可用低级烷氧基、羧基低级烷氧基、芳基低级烷氧基或杂环取代的亚氨基;也可用氨基甲酰基或低级烷氧基羰基取代的腙基;也可用低级烷基或氨基取代的氨基甲酰基;也可用低级烷基取代的硫代氨基甲酰基;也可用取代基(低级烷基、酰基、低级烷氧基羰基或低级烷基磺酰基取代的氨基;硝基;酰氧基;也可用卤素或羧基取代的低级烷基;卤素;低级烷氧基;羧基;低级烷氧基羰基;低级烯氧基羰基;或胍基)的芳基;或也可用卤素或低级烷基取代的杂环〕;也可用卤素、羟基、环烷基、低级烷氧基羰基或芳基取代杂环基取代的低级烯基;也可具有卤素的低级炔基;或环烯基(以下,Y简称Y2)的化合物、更优选的是Y是低级烷氧基羰基、芳基、低级烷基芳基、卤代芳基、低级烷氧基芳基、也可用杂环或酰基取代的低级烷基;或也可用羟基、卤素或芳基取代的低级烯基(以下,Y简称Y3)的化合物、最优选的是Y是异丙基、乙氧基羰基甲基、苄基、甲基苯基甲基、氟苯基甲基、三氯苯基甲基、甲氧基苯基甲基、吡啶基甲基、苯甲酰基甲基、丙烯基、甲基丙烯基、甲基丁烯基、羟甲基丁烯基、戊烯基、甲基戊烯基、二甲基辛二烯基、氯丙烯基、二氯丙烯基、溴丙烯基、二溴丙烯基、氟丙烯基、二氟丙烯基、丁烯基、溴丁烯基、氯丁烯基、苯基丙烯基(以下,Y简称为Y4)的化合物、18)、R1是R1-1、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-1、R7是R7-1、R8是R8-1、R9是R9-2、R10是R10-1、R11是R11-1、R12是氢、R13是R13-1、X是X1、Y是Y1、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、19)、R1是R1-2、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-1、R7是R7-1、R8是R8-1、R9是R9-1、R10是R10-1、R11是R11-1、R12是氢、R13是R13-2、X是X1、Y是Y1、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、20)、R1是R1-2、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-1、R10是R10-1、R11是R11-1、R12是氢、R13是R13-1、X是X1、Y是Y2、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、21)、R1是R1-1、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-2、R10是R10-1、R11是R11-1、R12是氢、R13是R13-2、X是X1、Y是Y1、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、22)、R1是R1-1、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-2、R10是R10-1、R11是R11-1、R12是氢、R13是R13-1、X是X1、Y是Y2、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、23)、R1是R1-1、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-1、R10是R10-1、R11是R11-1、R12是氢、R13是R13-2、X是X1、Y是Y2、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、24)、R1是R1-2、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-2、R10是R10-1、R11是R11-1、R12是氢、R13是R13-2、X是X1、Y是Y1、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、25)、R1是R1-2、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-2、R10是R10-1、R11是R11-1、R12是氢、R13是R13-1、X是X1、Y是Y2、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、26)、R1是R1-2、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-1、R10是R10-1、R11是R11-1、R12是氢、R13是R13-2、X是X1、Y是Y2或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、27)、R1是R1-1、R2是R2-1、R3是R3-1、R4是R4-1、R5是R5-1、R6是R6-2、R7是R7-1、R8是R8-2、R9是R9-2、R10是R10-1、R11是R11-1、R12是氢、R13是R13-2、X是X1、Y是Y2、或R1及R2、R1及R4、R8及R9或R13及-X-Y一起地形成含有1个以上的O或NR15(其中,R15与上述情况定义相同)的,可具有取代基的5~6元环的化合物、28)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y2、或R1及R4或R8及R9一起地形成含有1个以上的O的5~6元环的化合物、29)、R1是R1-3、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、30)、R1是R1-4、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成-OCH2O-的化合物、31)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y2、或R1及R4或R8及R9一起地形成含有1个以上的O的5~6元环的化合物、32)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-4、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、33)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、34)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-4、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、35)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、36)、R1是R1-3、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、37)、R1是R1-3、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、38)、R1是R1-3、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、39)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、40)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-3、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、41)、R1是R1-2、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、42)、R1是R1-3、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y2、或R1及R4或者R8及R9一起地形成-OCH2O-的化合物、43)、R1是R1-3、R2是R2-2、R3是R3-2、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-2、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成-OCH2O-的化合物、44)、R1是R1-3、R2是R2-2、R3是R3-3、R4是R4-2、R5是R5-2、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-2、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成-OCH2O-的化合物、45)、R1是R1-2、R2是R2-2、R3是R3-3、R4是R4-2、R5是R5-3、R6是R6-2、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X2、Y是Y3、或R1及R4或者R8及R9一起地形成含有1个以上的O的5~6元环的化合物、46)、R1是R1-3、R2是R2-2、R3是R3-3、R4是R4-2、R5是R5-3、R6是R6-3、R7是R7-2、R8是R8-2、R9是R9-3、R10是R10-2、R11是R11-2、R12是氢、R13是R13-3、X是X3、Y是Y4、或R1及R4或者R8及R9一起地形成-OCH2O-的化合物、47)、R1是R1-4、R2是R2-2、R3是R3-3、R4是R4-2、R5是R5-3、R6是R6-3、R7是R7-2、R8是R8-2、R9是R9-4、R10是R10-2、R11是R11-2、R12是氢、R13是R13-4、X是X3、Y是Y4、或R1及R4一起地形成-OCH2O-或者R8及R9为一起地形成-OCH2CH2O-的化合物、48)、具有以R1~R5作为取代基的苯环的以下的化合物、或
49)、具有以R6~R9作为取代基的苯环的以下的化合物、 或
50)、具有以R10~R13作为取代基的苯环的以下的化合物、 或
51)、Y是-CH2CH=CMe2、-(CH2)2CH=CMe2、-CH2CH=CCl2、-CH2CH=CBr2、-CH2CH=CF2、-CH2CH=CHMe、-CH2CH=C(Me)CH2OH、-CH2C≡CMe、-CH2C6H4-4-Me、-CH2C6H5、-CH2CH2CHMe2或者-Me的化合物、52)、-X-Y是-OCH2CH=CMe2、-O(CH2)2CH=CMe2、-OCH2CH=CCl2、-OCH2CH=CBr2、-OCH2CH=CF2、-OCH2C≡CMe、-OCH2C6H4-4-Me、-OCH2C6H5、-NHCH2CH=CMe2、-N(Me)CH2CH=CMe2、-NHCH2CH2CHMe2、-NHCH2C≡CH或-NMe2的化合物或53)R1~R13的取代基中,至少7个是氢的化合物,优选的是至少8个是氢的化合物,最优选的是至少9个氢的化合物、其药学上可接受的盐、它们的水合物或它们的药物前体。
以下,说明化合物(I_)的制备方法。
化合物(I_)的制备方法〔a法〕
化合物(I_),如下所示,可通过用通式(II)或(II′)表示的甲硼烷化合物和用通式(III)或(III′)表示的联苯衍生物进行反应而制备的。(式中,R1~R13、X及Y与上述式(I_)时的定义相同、A及Z与上述式(II)及(III)时的定义相同)或(式中,R1~R13、X及Y与上述式(I_)时的定义相同、A及Z与上述式(II)及(III)时的定义相同)。
将化合物(II)及化合物(III)或化合物(II′)及化合物(III′)在适宜的溶剂(例如苯、甲苯、二甲基甲酰胺、二甲氧基乙烷、四氢呋喃、二噁烷、乙醇、甲醇等)和水的混合系或无水系中,钯催化剂(例如Pd(PPh3)4、PdCl2(PPh3)2、PdCl2(OAc)2、PdCl2(CH3CN)2等,优选的是在Pd(PPh3)4存在下,碱性条件(K3PO4、NaHCO3、NaOEt、Na2CO3、Et4NCl、Ba(OH)2、Cs2CO3、CsF、NaOH、Ag2CO3等)下,室温~加热下反应数十分钟~数十小时,得到化合物(I_)。
相互反应的化合物的取代基A及Z的一方,只要是适用于铃木反应(Chemical Communication 1979,866、有机合成化学协会志,1993年,第51卷,第11号,第91页~第100页)的甲硼烷基就可以,优选的是二羟基甲硼烷。另外,另一方,只要是适用于铃木反应的离去基就可以,例如可使用卤素或-OSO2(CqF2q+1)(其中,q是0~4的整数)等。特别优选的是卤素或三氟甲磺酰氧(以下称为OTf)等,最优选的是溴、碘或OTf。
化合物(II)、(III)、 (II′)及(III′)的取代基R1~R13及-X-Y,只要是对于铃木反应无影响的基团,例如卤素、-OSO2(CqF2q+1)(其中,q是0~4的整数)以外的基团哪一种都可以。
例如,Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基。但是,即使R1~R13及Y是卤素,只要是取代基A与取代基Z的反应性比它的高,本反应就可顺利地进行。
另外,即使R1~R13或-X-Y中任何1个是羟基,也可进行上述反应,但此时,优选的是用通常使用的羟基保护基(例如甲氧基甲基、苄基、叔丁基二甲基甲硅烷基、甲磺酰基、对甲苯磺酰基等)保护后,加在上述反应上,然后,进行通常的脱保护反应。
作为合成化合物(I_)的方法,利用上述的铃木反应是最有效、且简单的,但是使用硅、锌、锡等代替上述图中的甲硼烷基进行反应也是可能的。
例如,A及Z的一方是-SiR17 3-r(Hal)r(其中,R17可以是各个不同的低级烷基、Hal是卤素、r是1~3的整数)、另一方是卤素或-OSO2(CqF2q+1)(其中,q是0~4的整数)时,使用通常使用的钯催化剂,进行偶合反应(Synlett(1991)845~853;J.Org.Chem.1996,61,7232-7233)。优选的钯催化剂的例子,可举出(i-Pr3P)2PdCl2,[(dcpe)PdCl2](dcpe=Cy2PCH2CH2PCy2)、(η3-C3H5PdCl2等。
另外,A及Z的一方是SnR3 18(其中,R18也可是分别不同的低级烷基)、另一方也可是卤素、乙酰氧基或-OSO2(CqF2q+1)(其中,q是0~4的整数)、使用通常所用的钯催化剂(优选的是Pd(PPh3)4等)可得到目的化合物(Angew.Chem.Int.Ed.Eng 1.25(1986)508-524)。
A及Z的一方是-Zn(Hal)(其中,Hal是卤素),与另一方是卤素的化合物反应也可合成目的化合物(Acc.Chem.Res.1982,15,340-348)。钯催化剂,只要是通常可使用的就可以,但作为优选的例子可举出Pd(PPh3)4、PdCl2(dppf)2、PdCl2(PPh3)2、PdCl2(P(o-Tolyl)3)2Pd(OAc)2等。
这些反应,都是在适当的溶剂中(例如二甲基甲酰胺、四氢呋喃等)、室温~加热下,反应数十分钟~数十小时就可以。
化合物(I_)的制备方法〔b法〕
作为制备化合物(I_)的更简便方法,有用如下所示通式(IV)、(V)及(VI)所示的化合物进行反应的方法(式中,R1~R13、X及Y与上述式(I)、(II)及(III)时定义相同、A1、A2、Z1及Z2分别与上述A及Z定义相同。但是,在化合物(IV)中,A1是具有比A2反应性高的或相同的反应性的基团、在化合物(IV′)中,A2是具有比A1反应性高或相同的反应性的基团)。
在用本合成法合成化合物(I_)时,首先,在化合物(IV)中加入化合物(V)进行反应,不分离由此生成的化合物,而继续加入化合物(VI)进行反应即可。另外,相反地,首先使化合物(VI)与化合物(IV′)反应,再使化合物(V)与其反应,也可同样地得到目的化合物。
为了得到目的化合物,由于需要使取代基A1与取代基Z1、取代基A2与取代基Z2反应,所以优选的是取代基A1及A2是反应性不同的基团。例如在化合物(IV)中,A1优选的是碘、A2优选的是溴或-OTf。相反地,在化合物(IV′)中,A2优选的是碘、A1优选的是溴或-OTf。但是,化合物(IV)或(IV′)是对称化合物时,A1及A2是相同的基团,也可得到目的化合物。
取代基Z1及取代基Z2也可以是相同的基团,也可以是不同的基团。
本发明的其他各条件与制法(a)时相同。
上述化合物中,取代基R1~R13只要不影响反应的基(例如卤素、-OSO2(CqF2q+1)(其中,q是0~4的整数)以外的基)或不影响该反应的基,而通过通常使用的反应,可变换成R1~R13的基就可以。此时,按照各化合物的反应,在适宜的阶段,只要变换成R1~R13就可以。
例如,其中的一个取代基是甲酰基,而作为目的取代基是羟基时,例如使用拜耳-维里格(Baeyer-Villiger)反应等,一旦生成甲酰氧基后,在酸性条件下或碱性条件下,只要进行通常的水解反应就可以。具体地,在适当的溶剂(例如1,2-二氯乙烷、氯仿、二氯甲烷、四氯化碳、苯)中,使化合物与过酸(例如过醋酸、过苯甲酸、间氯过苯甲酸、三氟过醋酸、过氧化氢),在-20℃~加热下反应数分钟~数十小时,只要在酸性条件下(例如盐酸和加热)或碱性条件下(例如与氢氧化钠水溶液加热)下,使得到的甲酰氧基水解就可以。
另外,其中的一个取代基是甲酰基、作为目的的取代基是羟甲基时,只要使用硼氢化钠、硼氢化锂、硼氢化锌、硼氢化三乙基锂、氢化铝、二异丁基氢化铝等还原剂,在适于还原剂的适当的溶剂(例如甲醇、乙醇、异丙醇、二甲基亚砜、二甘醇二甲氧基乙烷、四氢呋喃、苯、甲苯、环己烷等)中,在-20℃~80℃,优选的是冰冷下~室温下,反应数十分钟~数小时就可以。
进而,在其中的一个取代基是甲酰基、作为目的的取代基是碳数增加了的烯基时,通过维悌希(Wittig)反应(有机反应(OrganicReaction))、1965年、第14卷、第270页)可得到目的化合物。
其中的一个取代基是甲酰基,作为目的的取代基是羧基时,只要使用亚氯酸钠、琼斯试剂、无水铬酸等氧化剂,适于氧化剂的叔丁醇、丙酮等溶剂中,在0℃~加热下反应数小时就可以。根据需要,只要添加2-甲基-2-丁烯、磷酸二氢钠等就可适宜地进行反应。
另外,在其中的一个的取代基是羟基,作为目的的取代基是取代低级烷氧基时,只要在碳酸钠、碳酸氢钠、碳酸钾、氢氧酸钙、氢氧化钡、碳酸钙等的碱存在下,适当的溶剂(例如四氢呋喃、丙酮、二甲基甲酰胺、乙腈等)中使相应的烷基化试剂反应就可以,但具体地通过碘代醋酸甲酯、氯代醋酸乙酯、氯代醋酸丙酯等,与目的相应的卤化物反应,可得到取代基是烷氧基羰基低级烷氧基的化合物。
在其中的一个取代基是羧基,作为目的的取代基是氨基甲酰基时,在适当的溶剂(例如四氢呋喃、二甲基甲酰胺、乙醚、二氯甲烷等)中,根据需要,用适当的活化剂(例如亚硫酰氯、酰卤化物、酸酐、活化酯等)进行活化,与氨、二甲胺等氨化合物,在0℃~加热下,反应数分钟~数小时、进行氨基甲酰化就可以。
其中的一个取代基是氢,作为目的的取代基是卤素时,在适当的溶剂(例如氯仿、二氯甲烷、四氯化碳、乙腈、硝基甲烷、醋酸、无水醋酸)中,根据需要,在路易斯酸、盐酸、磷酸等催化剂存在下,与通常所用的卤化剂(例如溴、氯、碘、硫酰氯、N-溴丁二酰亚胺、N-碘丁二酰亚胺等),在-20℃~加热下,反应数分钟~数十小时进行卤化就可以。
在得到化合物(I)时,如上所述,也可使具有取代基-X-Y的化合物(II)和化合物(III)、或具有取代基-X-Y的化合物(III′)和化合物(II′)直接反应,但也可以使具有可变换成取代基-X-Y的取代基-W的化合物(II)或(III′)与化合物(III)或(II′)反应,最后,使取代基-W变换成取代基~X-Y即可。
例如,在-W是羟基或被保护的羟基的化合物时,只要通过通常所用的反应,导入作为目的的低级烷基、低级烯基、低级炔基、酰基、环烷基、环烯基、芳基、杂环或低级烷氧基等就可以。
具体地,在得到X是-O-的化合物时,只要首先得到-W是羟基的化合物,将其溶解在适当的溶剂(例如二甲基甲酰胺、四氢呋喃、丙酮、苯、二噁烷、乙腈等)中,在其中加入碱金属或碱土类金属的氢氧化物或碳酸盐(例如碳酸钠、碳酸氢钠、碳酸钾、氢氧化钙、氢氧化钡、碳酸钙等)或叔胺(例如三乙胺等)等的碱性助剂。在其中加入用Y-V(V是卤素或-OSO2(CqF2q+1)(其中,q是0~4的整数)表示的化合物(例如,异戊烯基溴、环己烯基溴、肉桂基溴、1-溴-2-戊烯、拢牛儿基溴、5-溴-2-甲基-2-戊烯、1,3-二氯-2丁烯、3-氯丙炔、三氟甲磺酸异戊烯基酯、三氟甲磺酸环己烯基酯、1,3-三氯丙烯等),在-20℃~加热下,反应数分钟~数十小时,可得到-W被取代成-O-Y的目的化合物。
另外,在得到X是-CH2-、-NR14-或-S-的化合物时,首先在无水二氯甲烷、氯仿、四氯化碳等溶剂中,在吡啶、三乙胺等碱存在下,使-W是羟基的化合物与三氟甲磺酸酐进行反应,三氟甲磺酸化后,在钯、镍等催化剂存在下,在适当的溶剂(例如四氢呋喃、二甲基甲酰胺、乙醚、三甲氧基乙烷等)中,使Y-V′(V′是-CH2ZnI、-SH、-NHR14)反应,可得到目的化合物。
另外,在X是NR14时,在四氢呋喃、甲醇等适当的溶剂中,使W是NH2的化合物与酮或醛反应,使用适当的还原剂(例如硼氢化钠、硼氢氰基化钠、锌盐酸)等或通过接触还原法进行还原,可得到目的化合物。
另外,通过常规方法,使W是NH2的化合物与Y-V″(其中,Y是酰基、也可具有取代基的低级烷基磺酰基、也可具有取代基的芳基磺酰基、V″是卤素等离去基)反应,可得到-X-Y是NH-Y的化合物。
在得到X是-SO或-SO2-的化合物时,首先用上述方法得到X是-S-的化合物,使用间氯苯过甲酸等通常的氧化剂进行氧化,可得到目的化合物。
将本发明化合物之一的-X-Y是低级烯氧基的化合物,进一步溶解在乙醇、醋酸乙酯等溶剂中,使用Pd-碳粉末、白金、铑、铷、镍等催化剂进行加氢,可得到-X-Y是低级烷氧基的化合物。
另外,在二氯甲烷、氯仿、苯、己烷、叔丁醇等溶剂中,使-X-Y是低级烯氧基的化合物与间氯过苯甲酸等反应,可变成-X-Y是环氧化低级烷氧基的化合物。
另外,对于具有进行反应时成为障碍的取代基的化合物,将该基预先用适当的保护基保护,只要在适当的阶段,用通常的方法离去即可。例如羟基成为反应障碍时,只要用甲氧基甲基、甲磺酰基、苄基、三氟甲磺酰基、叔丁基二甲基甲硅烷基等保护、在适当的阶段离去就可以。
例如在用甲磺酰基保护羟基时,只要在二氯甲烷、氯仿、四氯化碳等溶剂中,在三乙胺、吡啶等碱存在下,使甲磺酰氯在冰冷下~室温下反应数小时就可以。在进行脱保护反应时,在二甲基亚砜、二甲基甲酰胺、四氢呋喃、二噁烷、二甲氧基乙烷等的溶剂中,加入1-4N的氢氧化钠、氢氧化钾、它们的水溶液、甲醇钠或溴化乙基镁等,在室温~加热下反应数十分钟~数小时就可以。
在将甲氧基甲基作为羟基的保护基时,只要在四氢呋喃、二噁烷、二甲氧基乙烷等溶剂中,在氢氧化钠、二异丙基乙胺等存在下,与氯甲基甲基乙醚反应就可得到被保护的羟基。在进行脱保护时,只要在甲醇、四氢呋喃、醋酸等溶剂中,使用盐酸、硫酸等,就可进行通常的脱保护反应。
在将叔丁基二甲基甲硅烷基作为保护基时,只要在二甲基甲酰胺、乙腈、四氢呋喃、二甲基甲酰胺、二氯甲烷等溶剂中,在咪唑、三乙胺、2,6-二甲基吡啶等存在下,与氯化叔丁基二甲基甲硅烷基、三氟甲磺酸叔丁基二甲基甲硅烷基酯等进行反应就可以。脱保护反应只要在四氢呋喃等溶剂中,与四丁基氟化铵等反应,就可使保护基离去。
首先,与上述工序相同地是公知的化合物(VIII)及化合物(IX)、或化合物(VIII′)及化合物(IX′)(A及Z是可通过铃木反应进行偶合反应的基;例如一端是二羟基甲硼烷、二低级烷氧基甲脱烷基的甲硼烷,另一端是卤素或-OSO2(CqF2q+1)(其中,q是0~4的整数)。D是卤素或-OSO2(CqF2q+1)(其中,q与前述相同)以外的基,得到化合物(VII)或化合物(VII′)。
另外,代替如上所述的甲硼烷基,使用具有-SiR17 3-r(Hal)(其中,R17分别也可以是各种不同的低级烷基、Hal为卤素、r是1~3的整数)、-SnR18 3(其中,R18也是分别不同的低级烷基)或-Zn(Hal)(其中,Hal是卤素)的取代基的化合物,进行相同的反应,也可得到目的化合物。
接着,将取代基D变换成适用于铃木反应的取代基A。
例如,D=氢时,在适当的溶剂(例如醋酸、氯仿、二氯甲烷、四氯化碳、水、醋酸-醋酸钠等)中,只要与卤化剂(例如溴、氯、碘、磺酰氯、N-溴丁二酰亚胺等)在-20℃~加热下,反应数分钟~数十小时,就可得到A=卤素的目的化合物。
另外,D是被保护的羟基时,在适当的溶剂(例如二氯甲烷、氯仿、四氢呋喃、苯)中,在碱(例如吡啶、三乙胺)的存在下,与三氟甲磺酰化剂(例如三氟甲磺酸酐、三氟甲磺酰氯等)在-20℃~加热下,反应数分钟~数十小时,得到A=OTf的目的化合物。
将得到的本发明的化合物也可进一步进行前体药物化。前体药物化,只要是通常所用的方法,任何一种方法都可以进行。例如,只要将本发明的化合物的任何一个位置上结合的羟基或氨基等,取代成一般前体药物化所用的基团就可以。作为一般的前体药物化的例子,可举出将羟基取代成可取代的酰氧基(其中,取代基是羧基、磺基、氨基或低级烷基氨基等)或膦酰氧基等。优选的是将取代在R1上的羟基取代成-OCOCH2CH2COOH、-OCOCH=CHCOOH、-OCOCH2SO3H、-OPO3H2、-OCOCH2NMe2、-OCO-Pyr(Pyr表示吡啶)等就可以。
本发明的选择性的IgE产生抑制剂包括从在从成熟B细胞分化成产生抗体细胞,到产生抗体的过程中,抑制产生IgE,且不抑制或微弱抑制同时产生的IgG、IgM和/或IgA的免疫球蛋白的产生。
“在从成熟B细胞分化成产生抗体细胞,到产生抗体的过程中,抑制IgE产生”是指通过抑制以下任一过程,来抑制IgE的产生,1)通过各种因子(例如IL-4、IL-5等的细胞因子、抗CD40抗体等)活化成熟B细胞的过程、2)活化了的B细胞向浆细胞等的产生抗体细胞分化的过程(具体地说是向产生IgE类抗体细胞转换的过程)和/或3)抗体细胞产生免疫球蛋白的过程(具体说是产生IgE的过程)。在抑制1)的“通过各种因子活化成熟B细胞的过程”时,不包括抑制该因子从其他的细胞等产生的过程。
“抑制IgE产生,且不抑制或微弱抑制同时产生的IgG、IgM和/或IgA的免疫球蛋白的产生”是指在可同时产生IgE以及IgG、IgM及IgA中任何一种以上的免疫球蛋白的状态中,只是抑制IgE产生到能充分抑制过敏性反应的程度,不对于生物体防御有关的免疫系统有坏影响的程度,未抑制IgG、IgM和/或IgA的产生。换言之,是指:①IgE产生的抑制和IgG、IgM和/或IgA产生的抑制的选择性是5000倍、优选的是10000倍、更优选的是15000倍、最优选的是20000倍以上,和/或②与不存在的情况下比较,抑制50%的IgE产生的浓度的5000倍、优选的是10000倍、更优选的是15000倍、最优选的是20000倍的浓度中,也不抑制50%以上的IgG、IgM和/或IgA的产生。“与不存在下比较,抑制50%的IgE产生的浓度”是指将在可产生IgE状态下,添加或不给与本发明的选择性的IgE产生抑制剂时的IgE产生量作为100%,将其产生量抑制在50%的浓度。IgE的产生抑制和IgG、IgM或IgA中任何一种,优选的是,与所有的产生抑制比较,只要具有IgE选择性,作为医药就是有用的。
进而,本发明的选择性的产生IgE抑制剂,在给药于由变应原感染的哺乳动物(包括人)时,用不抑制或微弱抑制IgM、IgG和/或IgA产生的用量,与非给药时比较,可抑制90%以上的IgE产生。该“变应原”只要是诱导IgE产生,且能引起过敏性反应的物质任何一种都可以,例如临床上可举出花粉、虱、室内尘埃、白蛋白、牛奶、大豆等,实验上可举出卵白白蛋白、牛γ球蛋白、牛血清白蛋白、杉花粉的抗原蛋白(CryjI、CryjII)、虱的抗原蛋白(DerfI、DerfII)等。“不抑制或微弱抑制IgM、IgG和/或IgA产生的用量”是指对于不给与本发明的选择性的IgE产生抑制剂时的IgG、IgM和/或IgA的产生量,其抑制率是10%以下,优选的是5%以下,最优选的是3%以下。
进而,本发明的选择性的IgE产生抑制剂抑制炎症性细胞向组织中浸润。“炎症性细胞”包括所有的淋巴细胞、嗜酸性白细胞、嗜中性白细胞及巨噬细胞,优选的是嗜酸性白细胞和/或嗜中性白细胞。
由于本发明的选择性的IgE产生抑制剂直接与B细胞作用,其作用是强的。进而,由于不影响与生物体防御反应有关的体液免疫,所以没有感染等副作用,而具有很多优点。
具有这样作用的物质,不论其结构如何,都可作为免疫抑制剂。作为其一个例子,可举出本发明的化合物(I)或(I″)。
本发明的化合物中包括具有抑制促细胞分裂反应和/或细胞因子反应的作用。
具体地说,具有对于T和/或B两种细胞非常强的抑制繁殖作用、IL-4和/或IL-5任何一种或两者都具有细胞因子产生抑制作用。细胞因子产生抑制作用具有不抑制IL-2产生,而抑制IL-4和/或IL
5产生的选择性。
本发明的免疫抑制剂或抗过敏性剂,对于脏器或组织移植的排异反应、由于骨髓移植引起的移植物对宿主反应、特应性过敏性疾病(例如支气管哮喘、过敏性鼻炎、过敏性皮炎等)、高嗜酸性白细胞症侯、过敏性结膜炎、全身性红斑狼疮、多发性肌炎、皮肤肌炎、硬皮症、MCTD、慢性关节风湿症、炎症性大肠炎、缺血再灌流的损害、花粉症、过敏性鼻炎、荨麻疹及干癣等过敏性疾病的预防或治疗是有用的。
在作为免疫抑制剂和/或抗过敏性剂给与本发明化合物时,可以经口的、非经口中任何一种方法给药。经口给药,只要用常法配制成片剂、颗粒剂、散剂、胶囊剂、丸剂、液剂、浆剂、粘膜剂或含剂等通用剂型就可以。非经口给药,例如可以肌肉内给药、静脉内给药等注射剂、栓剂、经皮肤吸收剂、吸入剂等通用的任何一种剂型适当给药。特别优选的是经口给药。
在本发明的化合物的有效量中,根据需要,加入适合于其剂型的赋形剂、粘合剂、湿润剂、崩解剂、润滑剂、稀释剂等各种医药用添加剂,可作成医药制剂。注射剂时,只要与适当的载体一起进行杀菌处理,作成制剂就可以。
具体地说,作为赋形剂,可举出乳糖、蔗糖、葡萄糖、淀粉、碳酸钙或结晶纤维素等,作为粘合剂,可举出甲基纤维素、羧甲基纤维素、羟基丙基纤维素、明胶或聚乙烯吡咯烷酮等,作为崩解剂可举出羧甲基纤维素、羧甲基纤维素钠、淀粉、藻酸钠、琼脂粉末或月桂基硫酸钠等,作为润滑剂,可举出滑石、硬脂酸镁或聚乙二醇等。作为栓剂的基剂,可以使用可可脂、聚乙二醇或甲基纤维素等。另外,对于配制液剂或乳浊性、悬浮性注射剂时,也可适宜添加通常使用的溶解辅助剂、悬浮化剂、乳化剂、稳定剂、保存剂、等渗透剂等,在经口给药时,也可加入矫味剂、芳香剂等。
作为本发明化合物的免疫抑制剂和/或抗过敏性剂的给药量,最好考虑患者的年龄、体重、疾病种类及程度、给药途径等后进行设定,但对于成人经口给药时,通常是0.05~100mg/kg/日、优选的是0.1~10mg/kg/日的范围。非经口给药时,根据给药途径有很大不同,但通常是0.005~10mg/kg/日、优选的是0.01~1mg/kg/日的范围内,只要将其分成1日1次~数次就可以。
以下,用实施例进一步详细地说明本发明,但本发明不受这些实施例限制。
实施例
在实施例中所用的略语的定义如下。
Bn 苄基
DME 1,2-二甲氧基乙烷
DMF N,N-二甲基甲酰胺
DMSO 二甲基亚砜
MCPBA 间氯过苯甲酸
MOM 甲氧基甲基
Ms 甲磺酰基
Py 吡啶基
TBS 叔丁基二甲基甲硅烷基
Tf 三氟甲磺酰基
Ts 对甲苯磺酰基
工序1 化合物1的合成
在化合物(III-1)10.63g(22.08mmol)的1,2-二甲氧基乙烷溶液300ml中,在室温下加入四(三苯基膦)钯(0)3.60g(3.12mmol)。在其中加入化合物2(9.50g,26.5mmol)的99%乙醇溶液80ml、2M碳酸钠水溶液125ml(250mmol)、在氩气氛围中,加热回流该反应悬浮液6小时。冷却后,过滤反应混合物,除去不溶物,用2N盐酸将滤液调成酸性后,用醋酸乙酯萃取。将萃取液用5%碳酸氢钠水溶液、饱和食盐水依次洗涤、干燥、浓缩。用硅胶层析(己烷-醋酸乙酯1∶1)精制残渣后,从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物1(11.57g;收率87%)。
工序2 化合物(I-2)的合成
在化合物l(9.30g;15.48mmol)的无水二氯甲烷悬浮液60ml中,在冰冷下,加入三乙胺3.24ml(23.22mmol),接着,加入甲磺酰氯1.80ml(23.22mmol),在相同温度下搅拌2小时。蒸出溶剂后,用1N盐酸80ml,将溶液调成酸性,用氯仿萃取。将萃取液用1N盐酸、5%碳酸氢钠水溶液、饱和食盐水洗涤、干燥、浓缩将残渣从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物(I-2)9.93g(收率95%)。
工序3 化合物3的合成
将化合物(I-2)9.76g(14.38mmol)和氯化钯(II)7.65mg(4.31mmol)的1,4-二噁烷溶液300ml,在氢气氛围下,在室温下搅拌15小时。用沸石过滤除去不溶物,浓缩滤液后,将残渣从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物3(8.43g;收率100%)。
工序4 化合物(I-3)的合成
在化合物3(4.01g;6.81mmol)的无水N,N-二甲基甲酰胺溶液40ml中,陆续加入碳酸钾1.45g(10.5mmol)和异戊烯溴1.21ml(10.5mmol)。在氮气氛围中,在室温下搅拌15小时后,将反应液注入到0.6%柠檬酸水230ml中,用醋酸乙酯将其萃取。将萃取液用5%柠檬酸、5%碳酸钠水溶液、饱和食盐水依次洗涤、干燥、浓缩。将残渣从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物(I-3)4.01g(收率90%)。
工序5 化合物(I-1)的合成
在化合物(I-3)3.80g(5.79mmol)的二甲基亚砜溶液38ml中,加入4N氢氧化钠15ml(60.0mmol),将反应混合物在60℃下加热4小时。冷却后,加入1N盐酸100ml,用醋酸乙酯萃取。将萃取液,用5%碳酸氢钠水溶液、饱和食盐水依次洗涤、干燥、浓缩。将残渣从甲醇中重结晶,得到无色结晶的化合物(I-1)1.72g(收率70%)。
参考例1 化合物2的合成
在室温下,将化合物4(80.0g;0.287mol)、叔丁基二甲基甲硅烷氯45.87g(0.296mol)和咪唑21.46g(0.315mol)的N,N-二甲基甲酰胺溶液330ml,搅拌19小时。将反应混合物注入到1升水中,用乙醚萃取。将萃取液用水、饱和食盐水依次洗涤、干燥、浓缩。用硅胶层析(己烷-醋酸乙酯50∶1)精制残渣,得到无色油状物的化合物5(97.20g;收率86%)。
在化合物5(97.20g;0.247mol)的无水四氢呋喃溶液850ml中,在氮气氛围下,在-70℃下加入1.66N正丁基锂-己烷溶液152ml(0.252mol),在相同温度下搅拌1.5小时。在-70℃下,在其中加入硼酸三异丙酯171ml(0.741mol),一边缓慢地上升到室温,一边搅拌3小时。在冰冷下加入水500ml、5%柠檬酸(320ml),在相同温度下搅拌30分钟。用醋酸乙酯萃取反应液,用水、饱和食盐水依次洗涤萃取液,干燥、浓缩。用硅胶层析(己烷-醋酸乙酯2∶1)精制残渣,得到无色结晶的化合物2(51.10g;收率58%)。
参考例2 化合物(III-1)的合成
工序1 化合物8的合成
在化合物7(化学学会志(Journal of Chemical Society)1925,1998记载)15.30g(62.4mmol)的1,2-二甲氧基乙烷300ml溶液中,在室温下加入四(三苯基膦)钯(O)3.60g(3.12mmol)。在其中加入化合物6(英国专利公开公报第2276162号记载)18.89g(74.9mmol)的99%乙醇溶液80ml、2M碳酸钠水溶液125ml(250mmol),在氩气氛围下,加热回流该反应悬浮液6小时。冷却后,过滤反应混合物,除去不溶物。用2N盐酸将滤液调成酸性后,用醋酸乙酯萃取。用5%碳酸氢钠水溶液、饱和食盐水依次洗涤萃取液、干燥、浓缩。用硅胶层析(己烷-醋酸乙酸1∶1)精制残渣后,从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物8(15.68g;收率97%)。
工序2化合物9的合成
在化合物8(15.34g;59.39mmol)的无水二氯甲烷240ml悬浮液中,在冰冷下加入三乙胺16.6ml(118.8mmol),接着,加入甲磺酰氯6.93ml(89.09mmol),在相同温度下搅拌2小时。蒸出溶剂后,用1N盐酸(100ml)将溶液调成酸性,用醋酸乙酯萃取。用1N盐酸、5%碳酸氢钠水溶液、饱和食盐水依次洗涤萃取液、干燥、浓缩。将残渣从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物9(17.24g;收率86%)。
工序3 化合物(III-24)的合成
在化合物9(17.03g;50.63mmol)醋酸悬浮液210ml中,在室温下加入醋酸钠6.23g(75.95mmol)和溴3.91ml(75.95mmol),在相同温度下搅拌16小时。在该反应悬浮液中加入溴3.91ml(75.95mmol),在50℃下搅拌4小时后,进而,加入溴3.91ml(75.95mmol),在50℃下搅拌3小时。将反应混合物注入到1M硫代硫酸钠水1升中,搅拌30分钟。滤出析出的结晶,水洗后,将结晶溶解在氯仿800ml中,用5%碳酸氢钠水溶液、饱和食盐水依次洗涤、干燥、浓缩。将残渣从己烷-醋酸乙酯中重结晶,得到无色结晶的化合物(III-24)(18.12g;收率86%)。
工序4 化合物10的合成
在化合物(III-24)(15.80g;38.05mmol)的1,2-二氯乙烷悬浮液400ml中,在室温下加入80%间氯过苯甲酸12.30g(57.05mmol),在相同温度下搅拌17小时。将反应混合物注入到0.2M硫代硫酸钠水360ml中,和氯仿萃取。将萃取液用0.2M硫代硫酸钠300ml、5%碳酸氢钠水溶液200ml×2依次洗涤、干燥、浓缩。将这样得到的残渣15.80g溶解在1,2-二甲氧基乙烷330ml中,在其中加入4N盐酸30ml(120mmol)。将反应混合物在50℃下搅拌12小时、冷却后,蒸出溶剂,用醋酸乙酯萃取残渣。将萃取液用5%碳酸氢钠水溶液、饱和食盐水顺次洗涤、干燥、浓缩,得到浅褐色结晶的化合物10(14.35g;收率97%)。
工序5化合物(III-1)的合成
与化合物(I-4)相同地从化合物10(12.0g;29.76mmol)得到无色结晶的化合物(III-1)12.63g(收率88%)。
工序1 化合物11的合成
在化合物(III-2)816mg(2mmol)的1,4-二噁烷40ml的溶液中,在室温下,加入四(三苯基膦)钯(0)114mg(0.1mmol)、化合物2 748mg(2.09mmol)、粉末无水磷酸钾589mg(2.77mmol)、在氮气氛围中,在85℃下加热23小时。将反应液冷却后,用醋酸乙酯萃取。将萃取液用2N盐酸、5%碳酸氢钠水、饱和食盐水依次洗涤、干燥、浓缩。用硅胶层析(己烷-醋酸乙酯4∶1)精制残渣,通过用戊烷结晶化,得到浅黄色结晶的化合物11(745mg;收率67%)。
(工序2)化合物(I-4)的合成
在化合物11(557mg;1mmol)的一氯甲烷10ml的溶液中,在室温下加入80%间氯过苯甲酸259mg(1.2mmol),搅拌15小时。将反应液注入到0.1M硫代硫酸钠水中,用醋酸乙酯萃取。将萃取液,用0.1M硫代硫酸钠水、5%碳酸氢钠水、饱和食盐水依次洗涤、干燥、浓缩。在得到的残渣650mg的甲醇5ml的溶液中,在冰冷下,加入1M甲醇钠的甲醇溶液2ml,搅拌30分钟。用2N盐酸将反应液调成酸性,用醋酸乙酯萃取,将其萃取液用饱和食盐水洗涤、干燥后浓缩。在得到的残渣647mg的四氢呋喃10ml的溶液中,在冰冷下,加入1M氟化四丁基铵的四氢呋喃溶液2ml,搅拌30分钟。将反应液,在冰冷下,注入到2N盐酸水中,调成酸性,用醋酸乙酯萃取。将醋酸乙酯层,用水、5%碳酸氢钠水、饱和食盐水依次洗涤、干燥、浓缩。用硅胶层析(己烷-醋酸乙酯2∶1)精制残渣,得到粉末状化合物(I-4)275mg(收率62%)。
(工序1) 化合物13的合成
在化合物12(有机化学志(Journal of Organic Chemistry)1987、52、4485)2.61g(10mmol)的二甲基甲酰胺溶液26ml中,在冰冷下,加入60%油性氢化钠400mg(10mmol)和氯甲基甲基醚836mg(11mmol)搅拌30分钟。将反应温度调到室温后,进而,搅拌1小时。在减压下浓缩反应液后,用醋酸乙酯萃取。将萃取液用5%碳酸氢钠水溶液、饱和食盐水依次洗涤、干燥、浓缩。将残渣从醋酸乙酯-己烷-戊烷中重结晶,得到化合物13(2.8g;92%)。
(工序2) 化合物14的合成
与化合物8相同地使用化合物13和化合物15(东京化成制),得到浅黄色油状物的化合物14(收率96%)。
(工序3) 化合物16的合成
在化合物14 1.38g(4.3mmol)的甲醇的悬浮液16ml中加入2N盐酸水4ml,在60℃加热下,搅拌1小时。在减压下,将反应液浓缩后,用醋酸乙酯萃取。将萃取液用5%碳酸氢钠水、饱和食盐水依次洗涤后、干燥、浓缩,得到黄色结晶性残渣的化合物16(1.12g;收率94%)。
(工序4) 化合物(III-2)的合成
在化合物16(1.12g;4.05mmol)的无水一氯甲烷溶液12ml中,在冰冷下加入三氟甲磺酸酐1.02ml(6.08mmol)、接着加入吡啶980ml(12.2mmol),搅拌30分钟。将反应温度提高到室温,进而搅拌2小时后,蒸出溶剂。将残渣用醋酸乙酯萃取,用5%碳酸氢钠水、饱和食盐水依次洗涤、干燥、浓缩。将得到的粗生成物用硅胶层析(己烷-醋酸乙酯9∶1)精制,得到白色结晶性残渣的化合物(III-2)1.23g(收率74%)。
实施例3 化合物(I-5)、(I-6)、(I-7)的合成
(工序1) 化合物(I-5)的合成
与实施例1所述的化合物1相同,从化合物(III-II)881mg(1.50mmol)、3-三氟甲基硼酸370mg(1.95mmol),合成化合物(I-5)634mg(0.972mmol)。收率是65%。
(工序2) 化合物18的合成
与实施例1的化合物3相同,从化合物(I-5)433mg(0.664mmol)合成化合物18(360mg;0.640mmol)。收率是96%。
(工序3) 化合物(I-6)的合成
与实施例1的化合物(I-3)相同,从化合物18(170mg;0.302mmol),合成化合物(I-6)185mg(0.293mmol)。收率97%。
(工序4) 化合物(I-7)的合成
与实施例1的化合物(I-1)相同,从化合物(I-6)150mg(0.238mmol),合成化合物(I-7)85mg(0.179mmol)。收率75%。
(工序1) 化合物19的合成
与参考例2的化合物10相同,从化合物7(40.03g;163mmol),合成化合物19(24.04g;103mmol)。收率63%。
(工序2) 化合物20的合成
在氮气流下,在甲苯10ml中加入碘(5.94g;23.39mmol)、叔丁基胺(5.0ml、47.8mmol),在室温下搅拌50分钟。在该溶液中加入化合物19(5.46g;23.43mmol)升温到室温,搅拌6天。将反应液注入到1M硫代硫酸钠水中,用醋酸乙酯萃取。用1M硫代硫酸钠水、饱和食盐水依次洗涤萃取液、干燥、浓缩,合成了化合物20(8.30g;23.16mmol)。收率99%。
(工序3) 化合物21的合成
与实施例1的化合物1相同,从化合物20(8.70g;24.20mmol),合成了化合物21(2.10g;4.87mmol)。收率20%。
(工序4) 化合物(III-11)的合成
与实施例1的化合物(I-2)相同,从化合物21(3.20g;7.42mmol),合成了化合物(III-11)2.61g(4.44mmol)。收率60%。
(工序1) 化合物22的合成
与参考例1相同,将化合物(I-1)1.53g(3.63mmol)进行甲硅烷基化,将粗生成物通过结晶化从甲醇中得到无色结晶的化合物22(2.62g,收率95%)。
(工序2) 化合物23的合成
在化合物22(2.38g;3.1mmol)的丙酮90ml的溶液中加入三甲胺-N-氧化物二水合物415mg(3.74mmol)、5%四氧化锇水溶液1.60ml(0.3mmol),在室温下搅拌1小时。在反应液中加入水20ml,接着,加入碳酸氢钠4.0g、亚硫酸氢钠4.0g,搅拌30分钟。在减压下浓缩反应液,用醋酸乙酯萃取残渣。用饱和食盐水洗涤萃取液,干燥、浓缩。
在如上所述得到的残渣2.46g的乙醇90ml的溶液中,在室温搅拌下,滴加过碘酸钠1.96g(9.16mmol)的水33ml的溶液40分钟。搅拌2小时后,在反应液中慢慢地少量地加入水100ml,过滤析出的沉淀物,通过干燥,得到粉末化合物23(1.98g;收率87%)。
(工序3) 化合物(I-9)的合成
在溴化亚丙基三苯基膦146mg(0.38mmol)的干燥四氢呋喃2.5ml的悬浮液中,在氮气氛围中,在0℃下加入叔丁醇钾32mg(0.29mmol)在相同温度下搅拌1小时。将反应液冷却到-78℃,加入化合物23(70mg;0.095mmol)的干燥四氢呋喃1.5ml溶液,在相同温度下搅拌30分钟,接着,在室温下搅拌1小时。将反应液注入到冰冷了的饱和氯化铵水溶液中,用醋酸乙酯萃取。用饱和食盐水洗涤萃取液,干燥、浓缩。
将上述得到的残渣70mg,与实施例2的工序2相同地进行脱甲硅烷基化。用硅胶层析(甲苯-醋酸乙酯4∶1)精制粗生成物,得到浅黄色结晶的化合物(I-9)37mg(收率93%)。
(工序1) 化合物(I-563)的合成
与实施例1所述的化合物1相同,从化合物(III-27)800mg(1.59mmol)、化合物2(1.25g;3.50mmol),得到无色结晶的化合物(I-563)850mg(收率86%)。
(工序2) 化合物(1-565)的合成
在化合物(I-563)120mg(0.193mmol)的1,2-二甲氧基乙烷3ml,醋酸乙酯1ml溶液中,在40℃,加入4N盐酸2.4ml,在相同温度下搅拌2小时20分钟。冷却反应液后,用饱和碳酸氢钠水溶液中和,用醋酸乙酯萃取。用饱和碳酸氢钠水溶液、饱和食盐水洗涤萃取液、干燥、浓缩。将得到的粗生成物,通过从己烷-醋酸乙酯中结晶化,得到浅黄色结晶的化合物(I-565)93mg(收率92%)。
(工序1) 化合物24的合成
将化合物(III-24)415mg(1.00mmol)悬浮在叔丁醇17.5ml、2-甲基-2-丁烯5.3ml的混合液中,接着,在室温下加入亚氯酸钠724mg(8.00mmol)和磷酸二氢钠二水合物968mg(6.20mmol)的水溶液6.7ml,在相同温度下搅拌4小时30分钟。在反应液中加入1M硫代硫酸钠溶液,用醋酸乙酯萃取。进而,用饱和碳酸氢钠水溶液萃取油层,用浓盐酸将水层调成酸性,再用醋酸乙酯萃取。用饱和食盐水洗涤萃取液,通过干燥、浓缩,得到无色结晶化合物24(384mg;收率89%)。
(工序2) 化合物(III-27)的合成
在化合物24(1.50g;3.48mmol)的叔丁醇悬浮液10ml中,在室温下加入三乙胺0.533ml(3.83mmol),接着,加入二苯基磷酸迭氮物0.825ml(3.83ml),在100℃下搅拌23小时。将反应液冷却后,加入水、用醋酸乙酯萃取,用饱和碳酸氢钠水溶液、饱和食盐水洗涤萃取液,干燥、浓缩。用硅胶层析(己烷-醋酸乙酸2.5∶1)精制残渣,得到无色泡状物的化合物(III-27)1.43g(收率82%)。
实施例6 化合物(I-480)的合成1-479的脱保护体 I-480在脱保护了化合物(I-479)的Boc基的化合物120mg(0.287mmol)的四氢呋喃2ml、甲醇0.5ml的溶液中,在0℃下加入3-甲基-2-丁烯醛33ml(0.34mmol)和3摩尔硫酸水溶液90ml(0.26mmol)、搅拌10分钟。进而,分成数次加入硼氢化钠19.6mg,在室温下搅拌1小时。在反应液中加入饱和碳酸氢钠水溶液,用醋酸乙酯萃取。用饱和食盐水洗涤萃取液、干燥、浓缩。用硅胶层析(己烷-醋酸乙酯3∶1)精制残渣,得到无色结晶的化合物(I-480)98mg(收率71%)。
实施例7 化合物(I-628)的合成
与实施例1所述的化合物1的合成相同,将化合物(III-44)1.2g(2mmol)和4-溴甲磺酰苯胺551mg(2.2mmol)反应,接着,与实施例1的工序2相同地进行脱甲硅烷基化。将得到的粗生成物,通过从醋酸乙酯-己烷中结晶化得到浅黄色结晶的化合物(I-628)760mg(收率73%)。
(工序1) 化合物25的合成
与参考例1所述的化合物5相同,用硅胶层析(醋酸乙酯∶己烷=1∶20)精制从化合物21 22.2g(52.7mmol)、咪唑8.95g(132mmol)、叔丁基二甲基甲硅烷氯17.5g(116mmol)得到粗的生成物后,通过从醋酸乙酯-己烷结晶化得到无色结晶的化合物2529.7g(收率85%)。
(工序2) 化合物(III-44)的合成
与参考例1所述的化合物2的合成相同,通过使化合物25 402.7g(610mmol)和1.08Ns-丁基锂-环己烷溶液678ml(814mmol)及硼酸三异丙酯282ml(1.22mol)依次进行反应,得到无色粉末的化合物(III-44)246g(收率65%)。
在氩气流下,将化合物20 2.87g(8.0mmol)溶解在二甲氧基乙烷32ml和乙醇8ml中,接着,加入化合物23.01g(8.4mmol)和2M碳酸钠水溶液16ml,将反应液脱气。在该溶液中加入四(三苯基膦)钯462mg(0.4mmol)后,加入回流2小时。在室温中冷却反应液后,加入4-甲硫苯基硼酸2.02g(12.0mmol)、四(三苯基膦)钯462mg(0.4mmol)、2M碳酸钠水溶液16ml、二甲氧基乙烷32ml、乙醇8ml,将反应液再脱气后,加热回流16小时。将反应液冷却到室温后,加入5%柠檬酸水100ml,在相同温度下搅拌1小时。在反应液中加入醋酸乙酯,用5%柠檬酸水、水、饱和碳酸氢钠水溶液、饱和食盐水洗涤有机层、干燥、浓缩。用硅胶层析(己烷-醋酸乙酯3∶1)精制残渣,得到粗结晶2.13g。将得到的粗结晶从己烷-醋酸乙酯中进行重结晶,得到无色结晶的1.66g(收率44%)的化合物(I-233)。
实施例9 其它的化合物(I)的合成
以下,同样地合成以下的化合物(I)。以下,表示化合物(III)及化合物(I)的结构及物理常数。 表1
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III-1 | m.p.201-203℃1HNMR(DMSO-d6)δ3.44(s,3H),3.48(s,3H),3.62(s,3H),3.92(s,3H),7.09(s,1H),7.40-7.53(m,2H),7.65-7.78(m,2H) |
III-2 | 1HNMR(CDCl3)δ3.47(s,3H),3.94(s,3H),7.13-7.24(m,3H),7.50-7.59(m,2H),10.41(s,1H)IR(KBr)1700,1562,1479,1438,1393,1226,1199,1180,1161,1076,1047cm-1 |
III-3 | m.p.181-182℃1HNMR(CDCl3)δ3.21(s,3H),3.40(s,3H),3.49(s,3H),3.90(s,3H),4.81(s,2H),4.85(s,2H),6.86(s,1H),7.32-7.40(m,2H),7.60-768(m,2H)IR(KBr)1504,1467,1370,1235,1152,1038,1010,870,846,785cm-1 |
III-4 | 1HNMR(CDCl3)δ2.95(s,3H),3.18(s,3H),3.21(s,3H),3.41(s,3H),3.91(s,3H),6.84(s,1H),7.37(d,J=8.9Hz,2H),7.63(d,J=8.9Hz,2H) |
III-5 | m.p.140-141℃1HNMR(CDCl3)δ3.21(s,3H),3.45(s,3H),3.48(s,3H),3.96(s,3H),7.40(d,J=8.9Hz,2H),7.54(d,J=8.9Hz,2H)IR(KBr)1446,1426,1409,1370,1362,1184,1153,1029,973,920,870,849,776cm-1 |
III-6 | 东京化成制 |
III-7 | 1HNMR(CDCl3)δ:3.51(s,3H),3.92(s,3H),6.05(s,2H),6.92(d,J=8.1Hz,1H),7.02(d,J=8.1Hz,1H),7.07(s,1H),7.18(s,1H),10.40(s,1H)IR(KBr)1691,1600,1577,1474,1447,1422,1388,1352,1252,1237,1227,1201,1134,1124,1082,1038cm-1 |
III-8 | 1HNMR(CDCl3)δ3.20(s,3H),3.77(s,3H),3.90(s,3H),6.86(s,1H),6.98(s,1H),7.32-7.37(m,2H),7.51-7.56(m,2H) |
III-9 | HNMR(CDCl3)δ3.020(s,3H),3.34(s,3H),7.37-7.47(m,3H),7.53-7.63(m,3H),7.71(d,J=2.1Hz,1H) |
III-10 | 1HNMR(CDCl3)δ3.76(s,3H),3.90(s,3H),6.85(s,1H),6.97(s,1H),7.08-7.15(m,2H),7.42-7.49(m,2H) |
III-11 | oil1HNMR(CDCl3)δ2.72(s,3H),3.11(s,3H),3.75(s,3H),3.92(s,3H),5.17(s,2H),7.05-7.16(m,2H),7.24-7.50(m,2H). |
III-12 | 油状物1HNMR(CDCl3)δ3.51(s,3H),3.70(s,3H),3.86(s,3H),3.89(s,3H),5.28(s,2H),6.65(s,1H),6.97&7.47(ABq,J=8.6Hz,4H) |
III-13 | m.p.120-122℃1HNMR(CDCl3)δ3.20(s,3H),3.53(s,3H),3.70(s,3H),3.89(s,3H),5.28(s,2H),6.63(s,1H),7.32-7.37(m,2H),7.56-7.61(m,2H)IR(KBr)1505,1468,1427,1375,1237,1175,1153,1100,1072,1003,972cm-1 |
III-14 | m.p146-147℃1HNMR(CDCl3)δ3.85(s,3H),6.94-7.01(m,2H),7.38-7.56(m,6H)IR(KBr)1603,1522,1481,1288,1255,1036cm-1 |
III-15 | 1HNMR(CDCl3)δ3.07(s,6H),3.49(s,3H),3.92(s,3H),6.95(brs,2H),7.20(s,1H)7.51(d,J=8.7Hz,2H),10.42(s,1H) |
III-16 | 1HNMR(CDCl3)δ3.48(s,3H),3.50(s,3H),3.92(s,3H),6.81(s,1H),7.70(s,4H) |
III-17 | 1HNMR(CDCl3)δ3.24(s,3H),3.49(s,3H),3.94(s,3H),7.21(s,1H),7.42(d,J=8.4Hz,2H),7.65(d,J=8.4Hz,2H),10.41(s,1H) |
III-18 | m.p.88-89℃1HNMR(CDCl3)δ2.20(s,3H),2.38(s,3H),3.19(s,3H),7.06(s,1H),7.33(s,4H),7.45(s.1H)IR(KBr)1479,1366,1195,1173,1151,970,865,850,796cm-1 |
III-19 | m.p.72-73℃1HNMR(CDCl3)δ3.20(s,3H),7.20(dd,J=6.6,84Hz,1H),7.35-7.44(m,3H),7.53-7.60(m,2H)IR(KBr)1514,1481,1364,1335,1182,1144,979,870,798cm-1 |
III-20 | m.p.144-146℃1HNMR(CDCl3)δ3.45(s,3H),3.89(s,3H),4.99(brs,2H),6.19(s,1H),6.42(s,1H),6.88-6.94(m,2H),7.44-7.49(m,2H)IR(KBr)3471,3392,29863,1612,1596,1461,1410,1223,1175,1099,1079,1011cm-1 |
III-21 | 油状物1HNMR(CDCl3)δ1.09(t,J=7.5Hz,3H),1.82-1.94(m,2H),3.58(s,3H),3.86(s,3H),4.06(t,J=6.6Hz,2H),6.63(s,1H),6.94-6.99(m,2H),7.44-7.49(m,2H)IR(film):3100-2800(br),1609,1583,1513,1466,1423,1401,1378,1291,1249,1232,1178,1127,1097,1034,1012cm-1 |
III-22 | m.p.83.5-84.5℃1HNMR(CDCl3)δ3.20(br,1H),3.54(s,3H),3.85-3.90(m,2H),3.86(s,3H),3.90(s,3H),4.29-4.32(m,2H),6.66(s,1H),6.95-7.00(m,2H),7.45-7.50(m,2H)IR(KBr)36000-2800(br),1608,1583,1513,1467,1441,1421,1398,1365,1290,1247,1178,1133,1097,1079,1028,1007cm-1 |
III-23 | m.p99-101℃1HNMR(CDCL3)δ3.20(s,3H),3.39(s,3H),3.91(s,3H),3.99(s,3H),6.89(s,1H),7.37(d,J=8.7Hz,2H),7.64(d,J=8.7Hz,2H)IR(KBr)1747,1466,1367,1348,1153,1059,968,859,794cm-1 |
III-24 | 1HNMR(CDCl3)δ3.22(s,3H),3.45(s,3H),3.94(s,3H),7.04(s,1H),7.32-7.43(m,2H),7.58-7.69(m,2H),10.42(s,1H) |
III-25 | 1HNMR(CDCl3)δ2.46(broad,1H),3.21(s,3H),3.43(s,3H),3.90(s,3H),4.94(s,2H),6.83(s,1H),7.42-7.51(m,2H),7.57-7.68(m,2H) |
III-26 | m.p.109-110℃1HNMR(CDCl3)δ1.97(br,1H),3.21(t,J=6.6Hz,2H),3.86(s,3H),3.89(s,3H),3.90(t,J=6.9Hz,2H),6.76(s,1H),6.95-7.00(m,2H),7.49-7.53(m,2H)IR(KBr)3600-2800(br),1609,1581,1511,1462,1441,1426,1385,1289,1250,1237,1179,1116,1078,1046,1031,1005cm-1 |
III-27 | foam1HNMR(CDCl3)δ1.52(s,9H),3.20(s,3H),3.41(s,3H),3.90(s,3H),6.16(s,1H),6.76(s,1H),7.35(d,J=8.7Hz,2H),7.61(d,J=8.7Hz,2H)IR(KBr)3371,1718,1505,1497,1367,1241,1151,872cm-1 |
III-28 | m.p.167-170℃1HNMR(CDCl3)δ2.73(s,3H),3.74(s,3H),3.92(s,3H),7.08-7.17(m,3H),7.31-7.36(m,2H)IR(CHCl3)2934,1593,1560,1512,1477,1436,1411,1372,1157,1107,1076,997,958,892,839,815cm-1 |
III-29 | m.p.140-142℃1HNMR(CDCl3)δ3.27(s,3H),3.79(s,3H),3.90(s,3H),6.86(s,1H),6.97(s,1H),7.29(ddd,J=8.4,2.2,0.9Hz,1H),7.39(dd,J=11.0,2.2Hz,1H),7.43(t,J=8.4Hz,1H)IR(KBr)1504,1421,1344,1225,1208,916,824cm-1 |
III-30 | 1HNMR(CDCl3)δ3.77(s,3H),3.91(s,3H),3.95(s,3H),6.87(s,1H),7.01(s,1H),7.56(d,J=8.1Hz,2H),8.09(d,J=8.1Hz,2H) |
III-31 | 1HNMR(CDCl3)δ3.78(s,3H),3.91(s,3H),6.88(s,1H),6.97(s,1H),7.60(d,J=8.1Hz,2H),7.71(d,J=8.1Hz,2H) |
III-32 | m.p.147-148℃1HNMR(CDCl3)δ3.79(s,3H),3.92(s,3H),6.89(s,1H),7.01(s,1H),7.64-7.69(m,2H),8.26-8.31(m,2H)IR(KBr)3600-2800(b),1595,1511,1490,1422,1354,1249,1215,1145,1106,1032cm-1 |
III-33 | 1HNMR(CDCl3)δ3.31(s,3H),3.53(s,3H),3.94(s,3H),7.19(s,1H),7.39(ddd,J=8.3,2.3,1.0Hz,1H),7.39(dd,J=10.3,2.3Hz,1H),7.43(t,J=8.3H2,1H),10.40(s,1H) |
III-34 | 1HNMR(CDCl3)δ0.13(s,6H),0.97(s,9H),2.51(s,3H),3.73(s,3H),3.93(s,3H),5.09(s,2H),6.84-6.99(m,2H),6.89(s,1H),7.05(s,1H),7.29-7.48(m,5H) |
III-35 | m.p.124-128℃1HNMR(CDCl3)δ2.62(s,3H),3.74(s,3H),3.91(s,3H),5.19(s,2H),7.00-7.18(m,4H),7.30-7.49(m,5H)IR(CHCl3)2930,1607,1517,1480,1369,1148,1118,1082,1025,969,872cm-1 |
III-36 | oil1HNMR(CDCl3)δ0.13(s,6H),0.96(s,3H),3.01(s,3H),3.69(s,3H),3.86(s,3H),4.81(s,2H),5.08(s,2H),6.88-6.94(m,3H),7.30-7.47(m,5H)IR(KBr)3023,2932,2858,1579,1512,1471,1381,1264,1120,1083cm-1 |
III-37 | 油状物1HNMR(CDCl3)δ0.78(t,J=7.5Hz,3H),1.03-1.25(m,2H),1.38-1.47(m,2H),3.68-3.72(m,2H),3.70(s,3H),3.86(s,6H),5.15(s,2H),5.63(s,1H),6.81(dd,J=1.8,8.4Hz,1H),6.86(s,1H),6.95-6.97(m,2H),7.36-7.46(m,5H)IR(CH3Cl):3543,3200-2800(br),1587,1511,1465,1412,1376,1285,1248,1118,1081,1031cm-1 |
III-38 | m.p.104-105℃1HNMR(CDCl3)δ3.11(s.3H),3.77(s,3H),3.90(s,3H),5.17(s,2H),6.84(s,1H),6.98(s,1H),71.1(d,J=8.7Hz,1H),7.37-7.48(m,6H),7.5I(d,J=2.4Hz,1H)IR(KBr)3600-2800(br),1503,1420,1389,1364,1246,1215,1185,1132,1117,1097,100cm-1 |
III-39 | m.p.134-136℃1HNMR(CDCl3)δ3.78(s,3H),3.91(s,3H),5.29(s,2H),6.86(s,1H),6.97(s,1H),7.17(d,J=8.7Hz,1H),7.31-7.51(m,7H),7.63(dd,J=2.4,8.7Hz,1H),8.01(d,J=2.4Hz,1H)IR(KBr)3434,1620,1532,1494,1413,1280,1222,1206,1133,1108,1037cm-1 |
III-40 | m.p.100-101℃1HNMR(CDCl3)δ3.55(s,3H),3.77(s,3H),3.90(s,3H),5.26(s,2H),6.84(s,1H),6.97(s,1H),7.16-7.31(m,3H)IR(KBr)3600-2800(br),1524,1503,1449,1401,1380,1268,1246,1222,1200,1156,1126,1098,1078,1030cm-1 |
III-41 | m.p109-110℃1HNMR(CDCl3)δ1.54(s,9H),3.76(s,3H),3.90(s,H),6.75(br,1H),6.84(s,1H),6.97(s,1H),7.21-7.29(m,2H),8.13(t,J=8.7Hz,1H)IR(KBr)3600-2800(br),1720,1593,1531,1509,1427,1393,1245,1223,1214,1201,1162,1137,1105,1029cm-1 |
III-42 | foam1HNMR(CDCl3)δ2.36(s,3H),3.74(s,3H),3.88(s,3H),6.69(dd,J=0.6,3.6Hz,1H),6.85(s,1H),6.99(s,1H),7.24-7.27(m,2H),7.23(dd,J=1.8,8.7Hz,1H),7.60(d,J=3.6Hz,1H),7.64(d,J=1.2Hz,1H),7.80-7.83(m,2H),8.02(d,J=8.4Hz,1H)IR(KBr)3600-2800(br),1508,1463,1444,1421,1373,1246,1216,1176,1132,1093,1038cm-1 |
III-42 | 泡沫1HNMH(CDCl3)δ2.36(s,3H),3.74(s,3H),3.88(s,3H),6.69(dd,J=0.6,3.6Hz,1H),6.85(s,1H),6.99(s,1H),7.24-7.27(m,2H),7.23(dd,J=1.8,8.7Hz,1H),7.60(d,J=3.6Hz,1H),7.64(d,J=1.2Hz,1H),7.80-7.83(m,2H),8.02(d,J=8.4Hz,1H)IR(KBr)3600-2800(br),1508,1463,1444,1421,1373,1246,1216,1176,1132,1093,1038cm-1 |
III-43 | foam1HNMR(CDCl3)δ3.14(s,3H),3.51(s,3H),3.93(s,3H),5.20(s,2H),7.17(d,J=8.4Hz,1H),7.20(s,1H),7.38(m,6H),7.59(d,J=1.8Hz,1H),10.40(s,1H)IR(CHCl3)2941,1703,1613,1603,1580,1513,1475,1426,1372,1295,1264,1169,1137,1112,1088,1044,971,954,932,838cm-1 |
III-44 | 1HNMR(CDCl3)δ0.20(s,6H),0.13(s,6H),0.77(s,9H),0.97(s,9H),3.73(s,3H),3.83(s,3H)),5.08(s,2H),6.06(s,2H),6.88-6.96(m,3H),7.01(s,1H),7.30-7.49(m,5H) |
III-45 | mp106-108℃1HNMR(CDCl3)δ3.21(s,3H),3.43(s,3H),394(s,3H),5.87(s,1H),7.39(d,J=9.0Hz,2H),7.55(d,J=9.0Hz,2H)IR(KBr)3410,1460,1422,1362,1146,1037,874,915,787cm-1 |
III-46 | mp123-124℃1HNMR(CDCl3)δ2.48(brs,1H),3.21(s,3H),3.43(s,3H),3.94(s,3H),4.93(brs,2H),6.83(s,1H),7.37(d,J=9.0Hz,2H),7.63(d,J=9.0Hz,2H)IR(KBr)3524,1463,1352,1233,1152,1009,979,869cm-1 |
III-47 | mp107-109℃1HNMR(CDCl3)δ1.93(s,6H),2.45(s,6H),4.75(brs,1H),6.87-6.96(m,4H)IR(KBr)3367,1612,1509,1433,1214,990,824cm-1 |
III-48 | 油状物1HNMR(CDCl3)δ1.14(t,J=6.9Hz,3H),1.46(1,J=6.9Hz,3H),3.58(q,J=6.9Hz,2H),3.58(q,J=6.9Hz,2H),6.19(s,1H),6.41(s,1H),6.86-6.92(m,2H),7.43-7.49(m,2H)IR(CHCl3)3688,3594,3502,2982,1612,1517,1172,1080,1026,925cm-1 |
III-49 | 1HNMR(CDCl3)δ0.02(s,6H),0.12(s,6H),0.90(s,9H),0.93(s,9H),4.54(s,2H),4.76(s,2H),6.84-6.89(m,2H),7.16-7.22(m,2H),7.37(s,1H),7.69(s,1H) |
III-50 | mp173-175℃1H NMR(CDCl3)δ3.21(s,H),3.47(s,3H),3.89(s,3H),6.15(s,1H),6.42(s,1H),7.24-7.37(m,2H),7.61-7.66(m,2H)IR(KBr)3408,2934,1604,1480,1360,1146,1089,1004,865,709,547cm-1 |
III-51 | mp156-158℃1HNMR(CDCl3)δ3.21(s,3H),3.39(s,3H),3.90(s,3H),6.05(s,1H),7.36-7.44(m,4H)IR(KBr)3410,2938,1505,1457,1413,1337,1194,1143,1084,1014,876,826,542,519cm-1 |
III-52 | mp181-183℃1HNMR(CDCl3)δ3.19(s,3H),3.88(s,3H),4.21-4.24(m,2H),4.39-4.42(m,2H),6.49(s,1H),7.45(ABq,J=8.7Hz,4H)IR(KBr)3435,1598,1505,1474,1425,1366,1178,1147,1113cm-1 |
III-53 | mp155-157℃1HNMR(CDCl3)δ-0.11-0.02(m,2H),0.33-0.44(m,2H),0.91(m,1H),3.20(s,3H),3.41(d,J=7.0Hz,2H),3.50(s,3H),3.92(s,3H),6.88(s,1H),7.51(ABq,J=8.6Hz,4H)IR(KBr)3434,1505,1472,1416,1386,1371,1357,1242,1179,1149,1084cm-1 |
III-54 | mp105-107℃1HNMR(CDCl3)δ3.20(s,3H),3.39(s,3H),3.89(s,3H),4.77(s,2H),6.40(s,1H),7.33-7.55(m,5H)IR(KBr)3411,1592,1572,1507,1482,1467,1437,1360,1339,1232,1204,1175,1148,1125,1092cm-1 |
III-55 | mp138-140℃1HNMR(CDCl3)δ1.14(t,J=7.0Hz,3H),3.59(q,J=7.0Hz,2H),3.88(s,3H),4.97(bs,1H),6.42(s,1H),6.86-6.94(m,2H),7.43-7.51(m,2H)IR(KBr)3384,3291,2978,1614,1593,1576,1519,1484,1469,1455,1436,1417,1366,1306,1285,1257,1203,1171,1127,1094,1029cm-1 |
III-56 | mp162-164℃1HNMR(CDCl3)δ2.77(s,3H),3.17(s,3H),3.75(s,H),3.92(s,3H),7.10(s,2H),7.35-7.43(m,4H)IR(CHCl3)1594,1561,1507,1478,1464,1374,1331,1178,1149,1109,1080,1000,970,894,871,844cm-1 |
III-57 | mp95-97℃1HNMR(CDCl3)δ2.35(s,3H),3.77(s,3H),6.84-6.87(m,2H),7.12(s,1H),7.13(s,1H),7.35-7.38(m,2H)IR(CHCl3)3596,2959,2939,2840,1611,1563,1517,1489,1464,1438,1384,1367,1329,1295,1258,1173,1102,1049,1035,1001,911,891,835cm-1 |
III-58 | mp173-175℃1HNMR(CDCl3)δ6.91-6.94(m,2H),7.31-7.34(m,2H),7.87(s,1H),8.09(s,1H),9.89(s,1H),10.28(s,1H)IR(CHCl3)3437,1685,1610,1516,1456,1394,1370,1270,1261,1238,1214,1173,1144,1053,1012,939,905,829,808,557,458cm-1 |
III-59 | mp173-175℃1HNMR(CDCl3)δ1.10(t,J=6.9Hz,3H),1.48(t,J=6.9Hz,3H),3.20(s,3H),3.47(s,3H),3.66(q,J=6.9Hz,2H),4.11(q,J=6.9Hz,2H),6.79(s,1H),7.32-7.39(m,2H),7.60-7.66(m,2H)IR(CHCl3)1502,1458,1372,1176,1148,1074,1023,967,870cm-1 |
III-60 | 1HNMR(CDCL3)δ2.17(s,3H),2.39(s,3H),3.19(s,3H),5.80(s,1H),6.71(s,1H),7.33(s,4H) |
III-61 | mp107-108℃1HNMR(CDCl3)δ3.21(s,3H),3.79(s,3H),4.04(s,3H),7.39(d,J=8.9Hz,2H),7.57(d,J=8.9Hz,2H),7.68(s,1H),10.17(s,1H)IR(KBr)1704,1422,1358,1224,1148,1090,1026,974,876cm-1 |
III-62 | mp121-122℃1HNMR(CDCl3)δ3.45(s,3H),3.47(s,3H),3.93(s,3H),4.68(s,2H),4.77(s,2H),7.22(s,1H),7.49(d,J=8.1Hz,2H),7.56(d,J=8.1Hz,2H),10.42(s,1H)IR(KBr)1695,1476,1422,1232,1189,1130,1040,860cm-1 |
III-63 | mp113-115℃1HNMR(CDCl3)δ2.18(s,3H),3.22(s,3H),3.89(s,3H),6.85(s,1H),7.11(s,1H),7.36(s,4H)IR(KBr)1497,1413,1354,1230,1146,1097,976,864cm-1 |
III-64 | 1HNMR(CDCl3)δ5.65(s,1H),7.18(s,1H),7.30-7.35(m,2H),7.46-7.50(m,3H) |
III-65 | 1HNMR(CDCl3)δ:1.30(d,J=7.2Hz,6H),2.96(quintet,J=7.2Hz,1H),3.82(s,3H),3.91(s,3H),5.92(brs,2H),6.91(s,1H),7.30(d,J=8.1Hz,2H),7.44(s,1H),7.49(d,J=8.1Hz,2H) |
III-66 | mp118-122℃1HNMR(CDCl3)δ3.80(s,3H),3.91(s,3H),5.88(s,2H),6.84-6.92(m,3H),7.39-7.47(m,3H)IR(KBr)3600-2800(br),1606,1517,1492,1461,1415,1397,1330,1265,1205,1171,1052cm-1 |
III-67 | mp227-230℃1HNMR(CDCl3)δ0.25(s,6H),1.02(s,9H),2.33(s,3H),2.82(s,2H),6.88-6.93(m,2H),7.16(s,1H),7.21-7.25(m,3H),8.11(s,1H)IR(KBr)3600-2800(br),1608,1514,1393,1346,1267,1167cm-1 |
III-68 | mp134-137℃1HNMR(CDCl3)δ3.00(s,6H),3.81(s,3H),3.91(s,3H),6.00(s,2H),6.77-6.82(m,2H),6.90(s,1H),7.41(s,1H),7.46-7.51(m,3H)IR(KBr)3600-2800(br),1601,1528,1494,1466,1439,1399,1362,1321,1198,1166,1118,1051cm-1 |
III-69 | mp144-148℃1HNMR(CDCl3)δ2.38(s,3H),2.82(s,3H),3.01(s,6H),7.79-7.83(m,2H),7.18(s,1H),7.27-7.31(m,2H),8.11(s,1H)IR(KBr)3600-2800(br),1612,1523,1443,1389,1328,1271,1160cm-1 |
III-70 | mp122-126℃1HNMR(CDCl3)δ0.10(s,9H),0.78(s,6H),2.96(s,6H),3.75(s,3H),3.84(s,3H),6.08(s,2H),6.72-6.78(m,2H),7.01(s,1H),7.22-7.29(m,2H)IR(KBr)3600-2800(br),1613,1528,1463,1416,1402,1360,1345,1251,1218,1195,1136,1092,1062,991cm-1 |
III-71 | 1HNMR(CDCl3)δ2.21(s,3H),2.37(s,3H),3.89(s,3H),5.19(s,2H),6.75(d.d,J=8.4&2.1Hz,1H),6.81(d,J=2.1Hz,1H),6.92(d,J=8.4Hz,1H),7.08(s,1H),7.30-7.50(m,6H) |
III-72 | oil1HNMR(CDCl3)δ2.51(s,6H),2.75(s,6H),5.15(s,2H),5.67(s,1H),6.94(s,1H),6.96(d,J=8.4Hz,1H),7.04(dd,J=2.1,8.4Hz,1H),7.18(s,1H),7.20(d,J=2.1Hz,1H),7.37-7.47(m,5H)IR(CHCl3)3032,3428,3000-2800(br),1730,1611,1525,1489,1455,1256,1171,1137,1100,1036cm-1 |
III-73 | 1HNMR(CDCl3)δ2.21(s,3H),2.37(s,3H),5.15(s,2H),5.69(br,1H),6.73(dd,J=8.4,1.8Hz,1H),6.89-6.99(m,2H),7.07(s,1H),7.26-7.46(m,6H) |
III-74 | 1HNMR(CDCl3)δ1.09(t,J=7.2Hz,3H),1.22(t,J=7.5Hz,3H),2.55(q,J=7.2Hz,2H),2.72(q,J=7.5Hz,2H),5.15(s,2H),5.70(s,1H),6.73(dd,J=8.4,1.8Hz,1H),6.89(d,J=1.8Hz,1H),6.95(d,J=8.4Hz,1H),7.04(s,1H),7.38-7.47(m,6H)IR(CHCl3)3542,2970,2933,1586,1508,1480,1384,1324,1290,1160,1127,1064,1011,930,898,879,857cm-1 |
III-75 | 1HNMR(CDCl3)δ2.04(s,3H),3.70(s,3H),3.90(s,3H),5.19(s,2H),5.50(m,1H),6.73(dd,J=2.1Hz,1H),6.97-7.00(m,2H),7.29-7.48(m,5H) |
III-16 | 1HNMR(CDCl3)δ2.04(s,3H),3.90(s,3H),5.15(s,2H),5.49(s,1H),5.74(s,1H),6.71(dd,J=8.1,2.1Hz,1H),6.85(d,J=2.1Hz,1H),6.99-7.03(m,2H),7.39-7.45(m,5H)IR(CHCl3)3529,2963,2940,1731,1587,1566,1510,1480,1455,1412,1382,1323,1290,1248,1128,1099,1009,935,879cm-1 |
III-77 | mp87-89℃1HNMR(CDCl3)δ2.20(s,3H),2.37(s,3H),5.18(s,2H),6.90-7.10(m,4H),7.30-7.51(m,6H)IR(CHCl3)1510,1482,1381,1298,1267,1233,1127,1008,952,875,812cm-1 |
III-78 | 1HNMR(CDCl3)δ1.25(d,J=6.9Hz,6H),2.24(s,3H),3.26(sept,J=6.9Hz,1H),5.20(s,2H),6.95(ddd,J=8.3,2.2,1.2Hz,1H),7.06(t,J=8.3Hz,1H),7.06(dd,J=1.19,2.2Hz,1H),7.10(s,1H),7.17(s,1H),7.32-7.51(m,5H)IR(KBr)1492,1420,1228,1203,1140,1012,989,841cm-1 |
III-79 | 1HNMR(CDCl3)δ2.43(s,3H),5.19(s,2H),7.06(t,J=8.9Hz,1H),7.18-7.48(m,10H)IR(KBr)1491,1437,1214,1135,890,810,748cm-1 |
III-80 | mp77-79℃1HNMR(CDCl3)δ3.921(s,3H),5.21(s,2H),6.90-6.99(m,3H),7.31-7.50(m,7H)IR(KBr)3600-2800(br),1518,1477,1418,1237,1212,1167,1140cm-1 |
III-81 | mp103-105℃1HNMR(CDCl3)δ2.16(s,3H),2.37(s,3H),2.42(s,3H),3.16(m,3H),5.21(s,2H),7.16-7.17(m,3H),7.24-7.27(m,1H),7.36-7.48(m,5H)IR(CHCl3)2940,1613,1514,1478,1455,1423,1366,1331,1292,1264,1176,1140,1126,1096,1045,1009,972,955,920,843cm-1 |
III-82 | 1HNMR(CDCl3)δ2.19(s,3H),3.88(s,3H),5.20(s,2H),6.84(s,1H),6.95(m,1H),7.03-7.05(m,3H),7.35-7.49(m,5H) |
III-83 | mp83-85℃1HNMR(CDCl3)δ2.19(s,3H),3.88(s,3H),3.91(s,3H),5.21(s,3H),6.76(dd,J=8.4,2.1Hz,1H),6.82(d,J=2.1Hz,1H),6.87(s,1H),6.93(d,J=8.4Hz,1H),7.08(s,1H),7.32-7.50(m,5H)IR(CHCl3)2962,2937,1613,1579,1499,1464,1455,1443,1421,1319,1249,1170,1140,1103,1029,1008,989,901,832cm-1 |
III-84 | 油状物1HNMR(CDCl3)δ1.44(d,J=6.9Hz,3H),2.19(s,3H),4.09(q,J=6.9Hz,2H),5.20(s,2H),6.82(s,3H),6.94-7.08(m,3H),7.32-7.49(m,6H)IR(CHCl3)3597,2928,1731,1609,1523,1494,1476,1387,1298,1261,1173,1127,1048,834cm-1 |
III-85 | 1HNMR(CDCl3)δ2.26(s,3H),2.52(s,3H),3.90(s,3H),4.59(brs,2H),5.20(s,2H),6.73-7.10(m,4H),7.27-7.52(m,6H) |
III-86 | 1HNMR(CDCl3)δ2.33(s,3H),2.81(s,3H),4.60(brs,2H),5.20(s,2H),6.92-7.18(m,4H),7.30-7.52(m,6H) |
I-1 | m.p.155.5-156℃1HNMR(acetone-d6)δ1.77(brs,3H),1.79(brs,3H),3.37(s,3H),3.73(s,3H),4.63(brd,J=6.6Hz,2H),5.52(m,1H),6.49(1H,s),6.83(dd,J=2.2and8.2Hz,1H),6.92(d,J=2.2Hz,1H),6.94(m,2H),6.96(d,J=8.2Hz,1H),7.54(m,2H),7.62(brs,1H),7.78(s,1H),8.64(brs,1H)IR(KBr)3393,2932,1611,1588,1522,1490,1117,1071,1001cl-3m-1 |
I-2 | 1HNMR(CDCl3)δ2.67(s,3H),3.13(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.19(s,2H),6.84(s,1H),7.15(d,J=8.6Hz,1H),7.30-7.50(m,9H),7.60-7.75(m,2H)IR(KBr)1373,1361,1179,1149,1079,874,799cm-1 |
I-3 | m.p.155-157℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.71(s,3H),3.21(s,3H),3.23(s,3H),3.56(s,3H),3.78(s,3H),4.64(d,J=6.6Hz,2H),5.43-5.55(m,1H),6.84(s,1H),7.09(d,J=8.4Hz,1H),7.30-7.42(m,4H),7.65-7.75(m,2H)IR(KBr)1519,1481,1364,1179,1153,1083,970,877,796cm-1 |
I-4 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.16(s,2H),6.44(s,1H),6.92-7.19(m,5H),7.34-7.44(m,5H),7.57-7.66(m,2H)IR(KBr)3538,3510,3460,3330,1605,1521,1490,1455,1247,1220,1120,1070,1010cm-1 |
I-5 | m.p.136-138℃1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.55(s,3H),3.80(s,3H),5.19(s,2H),6.86(s,1H),7.16(d,J=8.7Hz,1H),7.33-7.49(m,7H),7.55-7.69(m,2H),7.82-7.87(m,2H)IR(KBr)3433,2937,1609,1519,1474,1463,1364,1322,1295,1274,1235,1183,1167,1120,1095,1077,1016cm-1 |
I-6 | 泡沫1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.72(s,3H),3.24(s,3H),3.49(s,3H),3.80(s,3H),4.64(d,J=6.9Hz,2H),5.50(m,1H),6.86(s,1H),7.10(d,J=8.7Hz,1H),7.35(dd,J=2.1,8.7Hz,1H),7.39(d,J=2.1Hz,1H),7.55-7.69(m,2H),7.82-7.87(m,2H).IR(CHCl3)3030,1608,1518,1480,1369,1322,1269,1230,1179,1131,1120,1097,1081,1015cm-1 |
I-7 | m.p.92-94℃1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.46(s,3H),3.77(s,3H),4.62(d,J=6.9Hz,2H),5.31(m,1H),5.71(s,1H),5.85(s,1H),6.47(s,1H),6.93(dd,J=1.8,8.7Hz,1H),6.97(d,J=8.7Hz,1H),7.05(d,J=1.8Hz,1H),7.55-7.65(m,2H),7.83-7.91(m,2H).IR(KBr)3466,2939,1609,1587,1518,1498,1486,1464,1437,1406,1361,1324,1245,1216,1155,1125,1073cm-1 |
I-8 | 1HNMR(CDCl3)δ3.22(s,3H),3.45(s,3H),3.77(s,3H),4.74(s,2H),5.15(s,2H),6.93(s,1H),7.01(d,J=8.7Hz,2H),7.32-7.48(m,9H),7.73(d,J=90Hz,2H)IR(KBr)3400,1721,1612,1509,1471,1362,1242,1153,1040,1018cm-1 |
I-9 | 1HNMR(CDCl3)δ1.03(t,J=7.2Hz,3H),2.16(dq,J=7.2,6.0Hz,2H),3.46(s,3H),3.74(s,3H),4.68(d,J=5.4Hz,2H),5.70(m,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.96(brs,2H),7.07(brs,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3445,3369,1612,1578,1523,1489,1268,1243,1112,1102,1071,1011,998,944,824,805,781cm-1 |
I-10 | m.p.174-175℃1HNMR(CDCl3)δ3.11(s,3H),3.21(s,3H),3.45(s,3H),3.73(s,3H),4.49(brs,2H),5.18(s,2H),6.85(s,1H),7.15(d,J=8.4Hz,1H),7.27(dd,J=8.4Hz,J=2.1Hz,1H),7.35-7.49(m,8H),7.70(m,2H)IR(KBr)1519,1467,1360,1346,1331,1295,1272,1229,1180,1151,1122,1101,1081,1022,980,971,954,875,849,814,798,742,525cm-1 |
I-11 | 1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.22(s,6H),3.45(s,3H),3.74(s,3H),4.49(brs,2H),4.64(d,J=7.2Hz,2H),5.45-5.55(m,1H),6.85(s,1H),7.08(d,J=8.7Hz,1H),7.26(dd,J=8.7and2.1Hz,1H),7.33(d,J=2.1Hz,1H),7.36-7.41(m,2H),7.65-7.75(m,2H)IR(KBr)3553,3434,1516,1472,1365,1176,1150,973,871cm-1 |
I-12 | 1HNMR(DMSO-d6)δ1.72(s,3H),1.77(s,3H),3.35(s,3H),3.65(s,3H),4.20(brs,2H),4.47(brt,J=4.4Hz,1H),4.55(brd,J=6.6Hz,2H),5.40-5.57(m,1H),6.64(dd,J=8.2,2.0Hz,1H),6.70(d,J=2.0Hz,1H),6.75-7.00(m,4H),7.40-7.55(m,2H)IR(KBr)3435,1518,1475,1459,1261,1223,988cm-1 |
I-13 | 1HNMR(CDCl3)δ2.71(s,3H),2.84(s,3H),3.20(s,3H),3.42(s,3H),3.76(s,3H),5.13(s,2H),5.67(s,1H),6.90(s,1H),6.89-6.96(m,2H),7.00(m,J=1.8Hz,1H),7.32-7.50(m,7H),7.70(d,J=9.0Hz,2H) |
I-14 | m.p.140-141℃1HNMR(CDCl3)δ2.71(s,3H),2.83(s,3H),3.15(s,3H),3.21(s,3H),3.42(s,3H),3.77(s,3H),5.16(s,2H),6.90(s,1H),7.09(d,J=8.9Hz,2H),73.0-7.50(m,9H),7.70(d,J=8.9Hz,2H)IR(KBr)1642,1516,1467,1362,1180,1151,1118,1050,867,803,708cm-1 |
I-15 | m.p.161-162℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.72(s,3H),2.85(s,3H),3.21(s,3H),3.23(s,3H),3.42(s,3H),3.77(s,3H),4.61(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),6.90(S,1H),7.02(d,J=8.1Hz,1H),7.31-7.37(m,2H),7.38(d,J=8.9Hz,2H),7.70(d,J=8.9Hz,2H)IR(KBr)1643,1516,1467,1362,1277,1236,1180,1150,974,882,868,847,802,710cm-1 |
I-16 | m.p.206-207℃1HNMR(CDCl3)δ1.71(s,3H),1.76(s,3H),2.62(s,3H),2.69(s,3H),3.27(s,3H),3.71(s,3H),4.53(d,J=6.8Hz,2H),5.47(t,J=6.6Hz,1H),6.61(dd,J=8.3and2.1Hz,1H),6.71(d,J=2.1Hz,1H),6.86(d,J=8.7Hz,2H),6.87(d,J=8.3Hz,1H),6.95(s,1H),7.47(d,J=8.7Hz,2H),8.83(brs,1H),9.59(brs,1H)IR(KBr)3427,3020,1608,1517,1467,1379,1233,1053,1005,839,799,759,543cm-1 |
I-17 | m.p.171-172℃1HNMR(DMSO-d6)δ1.74(d,J=0.9Hz,3H),1.77(s,3H),2.97(s,3H),3.45(s,3H),3.51(s,3H),3.77(s,3H),4.65(d,J=6.6Hz,2H),5.48(m,1H),7.06-7.27(m,4H),7.48&7.74(ABq,J=9.0Hz,4H)IR(KBr)1523,1483,1394,1366,1271,1175,1151,1087,1071,872,861,847,796cm-1 |
I-18 | 1HNMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.44(s,3H),3.76(s,3H),4.63(d,J=6.6Hz,2H),4.99(s,1H),5.48-5.62(m,1H),6.00(s,1H),6.45(s,1H),6.88-6.97(m,2H),7.04(dd,J=9.0,9.0Hz,1H),7.15-7.29(m,2H),7.45-7.60(m,2H)IR(KBr)3393,1523,1490,1466,1403,1267,1229,1113,1070cm-1 |
I-19 | 1HNMR(CDCl3)δ2.56(s,3H),3.21(s,3H),3.52(s,3H),3.69(s,3H),5.19(s,2H),5.76(s,1H),6.92(dd,J=8.4and2.0Hz,1H),7.04(d,J=84Hz,1H),7.05(d,J=2.0Hz,1H),7.35-7.51(m,7H),7.60(d,J=8.6Hz,2H) |
I-20 | 1HNMR(CDCl3)δ2.69(s,3H),3.14(s,3H),3.21(s,3H),3.53(s,3H),3.71(s,3H),5.20(s,2H),7.18(d,J=8.7Hz,1H),7.34-7.50(m,9H),7.59(d,J=8.7Hz,2H) |
I-21 | m.p.94-95℃1HNMR(CDCl3)δ2.73(s,3H),3.21(s,3H),3.24(s,3H),3.53(s,3H),3.71(s,3H),4.65(d,J=6.9Hz,2H),5.50(t,J=6.9Hz,1H),7.12(d,J=8.6Hz,1H),7.36(dd,J=8.6and2.1Hz,1H),7.41(d,J=2.1Hz,2H),7.41(d,J=8.8Hz,2H),7.59(d,J=8.8Hz,2H)IR(KBr)1516,1367,1180,1152,1039,975,869,799cm-1 |
I-22 | m.p.148-150℃1HNMR(CDCl3)δ3.42(s,3H),3.65(s,3H),4.63(d,J=6.9Hz,2H),4.98(brs,1H),5.53(t,J=6.9Hz,1H),6.92-6.96(m,4H),7.07(s,1H),7.43(d,J=8.6Hz,2H)IR(KBr)3398,1612,1587,1523,1462,1410,1261,1211,1099,1036,984,952,919,838,815cm-1 |
I-23 | 1HNMR(CDCl3)δ2.28(t,J=6.3Hz,1H),2.60(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),4.78(d,J=6.3Hz,2H),5.18(s,2H),6.84(s,1H),7.06(d,J=9.0Hz,1H),7.29-7.48(m,9H),7.69(d,J=8.7Hz,2H) |
I-24 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.26(s,3H),2.50(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),4.57(d,J=6.2Hz,2H),5.51(t,J=6.2Hz,1H),6.83(s,1H),6.92(d,J=9.0Hz,1H),7.17-7.29(m,2H),7.36(d,J=8.7Hz,2H),7.70(d,J=8.7Hz,2H)IR(KBr)3434,1608,1512,1479,1364,1234,1175,1150,1078,1017cm-1 |
I-25 | 1HNMR(CDCl3)δ1.75(s,3H),1.80(s,3H),2.27(s,3H),3.46(s,3H),3.74(s,3H),4.57(d,J=6.2Hz,2H),4.95(s,1H),6.63(t,J=6.2Hz,1H),5.86(s,1H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.92(d,J=9.0Hz,1H),7.24(d,J=9.0Hz,1H),7.26(s,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3399,1612,1566,1581,1520,1486,1237,1115,1078,1001cm-1 |
I-26 | m.p.246-247℃1HNMR(DMSO-d6)δ5.16(s,3H),6.84-6.87(m,2H),7.05(s,2H),7.14(s,1H),7.32-7.43(m,3H),7.49-7.64(m,8H)IR(KBr)3600-3100(br),1594,1453,1387,1296,1253,1010cm-1 |
I-27 | 1HNMR(DMSO-d6)δ3.38(s,3H),3.43(s,3H),5.28(s,2H),7.36-7.54(m,8H),7.69-7.86(m,8H)IR(KBr)1488,1354,1286,1178,1151,1116cm-1 |
I-28 | m.p.162-163℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.19(s,3H),3.23(s,3H),4.64(d,J=6.6Hz,2H),5.25-5.48(m,1H),7.09(d,J=9.0Hz,1H),7.36-7.40(m,2H),7.52(dd,J=2.4,9.0Hz,1H),7.59(d,J=2.4Hz,1H),7.62(s,4H),7.63-7.69(m,2H)IR(KBr)1489,1363,1290,1177,1154,1115,971,860,809cm-1 |
I-29 | m.p.195℃1HNMR(DMSO-d6)δ1.72(s,3H),1.75(s,3H),4.57(d,J=6.3Hz,2H),5.45-5.50(m,1H),6.84-6.87(m,2H),6.98-7.11(m,3H),7.50-7.64(m,6H)IR(KBr)3600-3200(br),1609,1594,1497,1257,991cm-1 |
I-30 | m.p.145-148℃1HNMR(CDCl3)δ1.60-2.20(m,6H),2.72(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.92(m,1H),5.88(m,1H),6.02(m,1H),6.84(s,1H),7.12(d,J=8.6Hz,1H),7.34-7.40(m,4H),7.69(m,2H)IR(KBr)1517,1481,1390,1362,1270,1244,1180,1151,1077,1012,973,960,873,817,799,521cm-1 |
I-31 | m.p.108-110℃1HNMR(CDCl3)δ1.60-2.20(m,6H),3.46(s,3H),3.75(s,3H),4.86(m,1H),5.02(bs,1H),5.75(s,1H),5.90(m,1H),5.91(s,1H),6.00(m,1H),6.45(s,1H),6.90-7.07(m,5H),7.53(m,2H)IR(KBr)3485,1614,1523,1491,1457,1407,1312,1287,1269,1238,1195,1170,1115,1072,1014cm-1 |
I-32 | m.p.188-190℃1HNMR(CDCl3)δ2.69(s,3H),3.21(s,3H),3.26(s,3H),3.56(s,3H),3.78(s,3H),4.84(m,2H),6.42(dt,J=15.6Hz,J=5.7Hz,1H),6.79(d,J=15.6Hz,1H),6.84(s,1H),7.15(d,J=8.4Hz,1H),7.28-7.43(m,9H),7.68(m,2H)IR(KBr)1519,1479,1447,1391,1360,1301,1273,1241,1228,1201,1175,1152,1120,1079,1014,974,959,947,868,819,795,777,743,521cm-1 |
I-33 | m.p.157-159℃1HNMR(CDCl3)δ3.46(s,3H),3.75(s,3H),4.81(m,2H),4.93(bs,1H),5.70(s,1H),5.91(s,1H),6.45(s,1H),6.46(dt,J=15.9Hz,J=6.0Hz,1H),6.76(d,J=15.9Hz,1H),6.90-7.09(m,5H),7.26-7.46(m,5H),7.54(m,2H)IR(KBr)3466,1611,1522,1489,1461,284,1248,1192,1165,1114,1073cm-1 |
I-34 | m.p.127-129℃1HNMR(CDCl3)δ1.03and1.04(botht,bothJ=8.0Hz,total3H),2.07-2.19(m,2H),2.71and2.72(boths,total3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.60and4.71(bothm,total2H),5.66-5.75and5.90-5.99(bothm,total2H),6.84(s,1H),7.09(d,J=8.4Hz,1H),7.33-7.41(m,4H),7.68(m,2H)IR(KBr)1519,1482,1390,1362,1232,1180,1150,1077,974,873,815,799,522cm-1 |
I-35 | m.p.166-168℃1HNMR(CDCl3)δ1.04and 1.05(botht,bothJ=7.5Hz,total3H),2.09-2.19(m,2H),3.46(s,3H),3.74(s,3H),4.58and4.68(bothm,total2H),5.01(bs,1H),5.69-5.78and5.87-5.95(bothm,total4H),6.45(s,1H),6.90-7.06(m,5H),7.53(m,2H)IR(KBr)3531,3489,3306,1523,1492,1459,1408,1314,1287,1270,1255,1234,1224,1118,1072,1018,1005,822cm-1 |
I-36 | m.p.148-150℃1HNMR(CDCl3)δ1.62(s,3H),1.69(s,3H),1.76(s,3H),2.08-2.20(m,4H),2.71(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.66(d,J=6.3Hz,2H),5.09(m,1H),5.50(t,J=6.3Hz,1H),6.84(s,1H),7.10(d,J=8.4Hz,1H),7.33-7.41(m,4H),7.68(m,2H)IR(KBr)1519,1480,1464,1449,1389,1366,1291,1271,1233,1200,1176,1150,1118,1079,1012,973,946,876,841,816,801,523,510cm-1 |
I-37 | 1HNMR(CDCl3)δ1.58(s,3H),1.63(s,3H),1.70(s,3H),2.05-2.20(m,4H),3.46(s,3H),3.75(s,3H),4.64(d,J=6.3Hz,2H),4.95(bs,1H),5.11(m,1H),5.53(m,1H),5.70(s,1H),5.90(s,1H),6.45(s,1H),6.91-7.08(m,5H),7.54(m,2H) |
I-38 | m.p.149-151℃1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.55(m,2H),2.73(s,3H),3.21(s,3H),3.22(s,3H),3.56(s,3H),3.77(s,3H),4.07(t,J=6.8Hz,2H),5.21(m,1H),6.84(s,1H),7.08(d,J=8.2Hz,1H),7.32-7.40(m,4H),7.68(m,2H)IR(KBr)1520,1483,1389,1363,1296,1180,1151,1079,975,872,815,799,521cm-1 |
I-39 | m.p.105-107℃1HNMR(CDCl3)δ1.68(s,3H),1.75(s,3H),2.53(m,2H),3.54(s,3H),3.74(s,3H),4.06(t,J=6.8Hz,2H),5.01(bs,1H),5.22(m,1H),5.69(s,1H),5.90(s,1H),6.45(s,1H),6.90-7.06(m,5H),7.53(m,2H)IR(KBr)3477,3388,1523,1489,1469,1402,1285,1261,1248,1227,1196,1175,1164,1115,1100,1073,1011cm-1 |
I-40 | m.p.155-157℃1HNMR(CDCl3)δ1.89(t,J=2.4Hz,3H),3.45(s,3H),3.75(s,3H),4.74(q,J=2.4Hz,2H),5.00(bs,1H),5.66(s,1H),5.92(s,1H),6.45(s,1H),6.90-7.08(m,5H),7.54(m,2H)IR(KBr)3446,2224,1523,1488,1402,1266,1238,1203,1187,1166,1102,1068,1009cm-1 |
I-41 | 1HNMR(CDCl3)δ2.19(s,3H),3.45(s,3H),3.75(s,3H),4.62(m,2H),4.92(bs,1H),5.60(bs,1H),5.92(s,1H),5.99(m,1H),6.45(m,1H),6.91-7.08(m,5H),7.53(m,2H) |
I-42 | 油状物1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.87(s,3H),3.22(s,6H),3.55(s,3H),3.80(s,3H),4.66(d,J=7.5Hz,2H),5.61(m,1H),6.84(s,1H),7.37-7.41(m,3H),7.61(d,J=2.1Hz,1H),7.67(m,2H) |
I-43 | m.p.132-136℃1HNMR(CDCl3)δ1.74(s,3H),1.82(s,3H),3.44(s,3H),3.76(s,3H),4.62(m,2H),5.05(brs,1H),5.61(m,1H),5.79(s,1H),6.02(s,1H),6.44(s,1H),6.92(m,2H),7.04(d,J=2.1Hz,1H),7.20(d,J=2.1Hz,1H),7.53(m,2H)JIR(KBr)3495,3422,1611,1520,1473,1400,1355,1315,1280,1227,1194,1173,1111,1077,1023cm-1 |
I-44 | m.p.148-149℃1HNMR(CDCl3)δ1.60(s,3H),1.70(s,3H),2.32-2.39(m,2H),2.65(s,3H),2.76-2.81(m,2H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),5.16-5.21(m,1H),6.85(s,1H),7.30-7.40(m,5H),7.66-7.71(m,2H)IR(KBr)1480,1390,1361,1181,1150,1075cm-1 |
I-45 | m.p.73-75℃1HNMR(CDCl3)δ1.63(s,3H),1.72(s,3H),2.32-2.39(m,2H),2.64-2.70(m,2H),3.46(s,3H),3.74(s,3H),4.83(s,1H),4.95(s,1H),5.27-5.31(m,1H),5.92(s,1H),6.45(s,1H),6.89-7.00(m,4H),7.21(d,J=10.5Hz,1H),7.52-7.55(m,2H)IR(KBr)3600-3200(br),3100-2800(br),1612,1579,1523,1487,1452,1400,1360,1226,1174,1111,1072cm-1 |
I-46 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.65(m,2H),4.85(s,1H),5.33(m,1H),5.44(m,1H),5.67(s,1H),5.91(s,1H),6.10(m,1H),6.45(s,1H),6.92(m,2H),6.95(m,2H),7.08(m,1H),7.54(m,2H) |
I-47 | 1HNMR(acetone-d6)δ3.39(s,3H),3.72(s,3H),5.20(s,2H),6.48(s,1H),6.83(dd,J=2.0Hz,J=8.4Hz,1H),6.93(m,2H),6.96(d,J=2.0Hz,1H),7.04(d,J=8.4Hz,1H),7.34-7.45(m,3H),7.52(m,2H),7.52-7.58(m,2H)IR(CHCl3)3522,3348,1699,1612,1589,1521,1489,1458,1402,1288,1114,1071,935cm-1 |
I-48 | 1HNMR(acetone-d6)δ1.28(t,J=7.2Hz,3H),3.39(s,3H),3.72(s,3H),4.25(q,J=7.2Hz,2H),4.78(s,2H),6.49(s,1H),6.83(dd,J=1.8and8.4Hz,1H),6.93(m,2H),6.96(d,J=1.8Hz,1H),6.97(d,J=8.4Hz,1H),7.52(m,2H),7.63(s,1H),7.83(s,1H),8.50(s,1H) |
I-49 | 1HNMR(acetone-d6)δ1.75(m,3H),3.39(s,3H),3.72(s,3H),4.56(m,2H),5.71-5.82(m,1H),5.84-5.96(m,1H),6.48(s,1H),6.82(dd,J=2.0and8.4Hz,1H),6.93(d,J=2.0Hz,1H),6.93(m,2H),6.95(d,J=8.4Hz,1H),7.52(m,2H) |
I-50 | 1HNMR(ncetone-d6)δ1.75(m,3H),3.39(s,3H),3.72(s,3H),4.72(m,2H),5.73-5.75(m,2H),6.48(s,1H),6.83(dd,J=2.0and7.8Hz,1H),6.92-6.95(m,3H),6.97(d,J=7.8Hz,1H),7.52(m,2H) |
I-51 | 1HNMR(acetone-d6)δ1.77(s,3H),1.79(s,3H),3.41(s,3H),3.72(s,3H),4.66(m,2H),5.53(m,1H),6.49(s,1H),6.85(m,2H),7.04(d,J=8.1Hz,1H),7.10(dd,J=2.1and8.1Hz,1H),7.19(d,J=2.1Hz,1H),7.25(m,2H) |
I-52 | 1HNMR(CDCl3)δ2.58(t,J=2.2Hz,1H),2.73(s,3H),3.22(s,3H),3.26(s,3H),3.56(s,3H),3.78(s,3H),4.83(d,J=2.2Hz,2H),6.85(s,1H),7.21(d,J=8.4Hz,1H),7.35-7.46(m,4H),7.64-7.74(m,2H) |
I-53 | 1HNMR(CDCl3)δ3.45(s,3H),3.76(s,3H),4.36(d,J=1.5Hz,1H),4.55(s,2H),4.76(dd,J=1.8and0.6Hz,1H),5.02(brs,1H),5.97(d,J=0.9Hz,1H),6.45(s,1H),6.90-6.96(m,2H),6.96-7.05(m,2H),7.10-7.12(m,1H),7.50-7.58(m,2H |
I-54 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.61(s,3H),3.53(s,3H),3.77(s,3H),4.61(d,J=6.9Hz,2H),5.17(brs,1H),5.45-5.50(m,1H),5.72(s,1H),6.84(s,1H),6.88-7.00(m,4H),7.02(d,J=1.8Hz,1H),7.50-7.57(m,2H) |
I-55 | 1HNMR(CDCl3)δ0.99(d,J=6.5Hz,6H),1.74(q,J=6.5Hz,2H),1.85(m,1H),3.46(s,3H),3.75(s,3H),4.12(t,J=6.5Hz,2H),4.97(s,1H),5.65(s,1H),5.90(s,1H),6.45(s,1H),6.92(m,2H),6.95(m,2H),7.06(m,1H),7.54(m,2H) |
I-56 | 1HNMR(CDCl3)δ1.34(s,3H),1.35(s,3H),3.15(dd,J=3.6and6.6Hz,1H),3.39(s,3H),3.72(s,3H),4.10(dd,J=6.6and11.1Hz,1H),4.34(dd,J=3.6and11.1Hz,1H),6.49(s,1H),6.83(dd,J=1.8and8.1Hz,1H),6.93(d,J=8.7Hz,2H),6.94(d,J=1.8Hz,1H),7.00(d,J=8.1Hz,1H),7.52(d,J=8.7Hz,2H) |
I-57 | 1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.53(s,3H),3.78(s,3H),5.19(s,2H),6.83(s,1H),7.10-7.19(m,3H),7.31-7.50(m,7H),7.57-7.64(m,2H)IR(KBr)1607,1520,1481,1373,1231,1176,1119,1078cm-1 |
I-58 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.72(s,3H),3.23(s,3H),3.53(s,3H),3.78(s,3H),3.78(s,3H),4.64(d,J=6.6Hz,2H),6.84(t,J=6.6Hz,1H),5.83(s,1H),7.06-7.20(m,3H),7.31-7.40(m,2H),7.56-7.65(m,2H)IR(KBr)1603,1521,1483,1376,1366,1176,1085cm-1 |
I-59 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.45(s,3H),3.75(s,3H),4.62(d,J=6.9Hz,2H),5.52(t,J=6.9Hz,1H),5.71(brs,1H),5.89(s,1H),6.44(s,1H),6.90-719(m,5H),7.56-7.67(m,2H)IR(KBr)3545,3385,1605,1586,1561,1520,1384,1311,1284,1225,1121,1096cm-1 |
I-60 | 1HNMR(CDCl3)δ 3.49(s,3H),3.74(s,3H),5.15(s,2H),5.68(s,1H),5.91(s,1H),6.02(s,2H),6.43(s,1H),6.88-7.19(m,6H),7.31-7.48(m,5H)IR(CHCl3)3535,1615,1588,1519,1500,1482,1410,1290,1241,1204,1092,1041cm-1 |
I-61 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.73(s,3H),3.23(s,3H),3.57(s,3H),3.77(s,3H),4.64(d,J=6.6Hz,1H),5.50(t,J=6.6Hz,1H),6.03(s,2H),6.83(s,1H),6.91(d,J=8.1Hz,1H),7.08(d,J=8.1Hz,1H),7.09(d,J=8.1Hz,1H),7.14(s,1H),7.34(d,J=8.1Hz,1H),7.39(s,1H)IR(CHCl3)1607,1518,1477,1453,1369,1240,1178,1081cm-1 |
I-62 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.49(s,3H),3.74(s,3H),4.61(d,J=6.9Hz,2H),5.53(t,J=6.9Hz,1H),5.68(s,1H),6.02(s,2H),6.43(s,1H),6.88-6.96(m,3H),7.03-7.18(m,3H)IR(KBr)3494,1610,1583,1561,1519,1480,1460,1409,1286,1243,1191,1127,1089,1036cm-1 |
I-63 | m.p.201-202℃1HNMR(CDCl3)δ3.78(s,6H),5.16(s,4H),5.69(s,2H),6.93(s,2H),6.99(d,J=8.4Hz,2H),7.08(dd,J=2.1and8.4Hz,2H),7.22(d,J=2.1Hz,2H),7.37-7.47(m,10H),IR(KBr)3600-3100(br),1584,1523,1454,1272,1245,1210,1130cm-1 |
I-64 | m.p.173-175℃1HNMR(CDCl3)δ3.12(s,6H),3.80(s,6H),5.18(s,4H),6.92(s,2H),7.12(d,J=8.7Hz,2H),7.36-7.50(m,12H),7.60(d,J=2.1Hz,2H)IR(KBr)1523,1492,1356,1290,1263,1210,1182,1114cm-1 |
I-65 | 1HNMR(CDCl3)δ1.76(d,J=0.9Hz,6H),1.81(d,J=0.6Hz,6H),3.22(s,6H),3.80(s,6H),4.63(d,J=6.6Hz,4H),5.48-5.53(m,2H),6.92(s,2H),7.05(d,J=8.4Hz,2H),7.48(dd,J=2.1and8.4Hz,2H),7.57(d,J=2.1Hz,2H)IR(KBr)1523,1492,1468,1353,1286,1258,1213,1174,1108cm-1 |
I-66 | 1HNMR(CDCl3)δ1.76(s,6H),1.82(s,6H),3.78(s,6H),4.62(d,J=6.9Hz,4H),5.50-5.55(m,2H),5.71(s,2H),6.91-6.94(m,4H),7.08(dd,J=2.1and8.4Hz,2H),7.57(d,J=2.1Hz,2H)IR(KBr)3600-3200(br),1523,1492,1271,1242,1210,1186,1034cm-1 |
I-67 | 1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.22(s,3H),3.28(s,3H),3.79(s,3H),3.80(s,3H),4.63(d,J=6.6Hz,2H),5.48-5.53(m,1H),6.92(s,1H),6.93(s,1H),7.06(d,J=8.4Hz,1H),7.13(d,J=8.4Hz,2H),7.42-7.51(m,3H),7.57(d,J=2.1Hz,1H)IR(KBr)3600-3200(br),1525,1493,1362,1293,1210,1172,1107cm-1 |
I-68 | m.p.168-169℃1HNMR(CDCl3)δ3.18(s,3H),3.78(s,3H),3.79(s,3H),5.17(s,2H),5.71(s,1H),6.92(s,1H),6.96(s,1H),6.99(d,J=8.7Hz,1H),7.08(dd,J=2.1and8.7Hz,1H),7.24(d,J=2.1Hz,1H),7.26-7.48(m,7H)IR(KBr)3600-3200(br),1488,1382,1369,1269,1206,1174,1146cm-1 |
I-69 | m.p.155-157℃1HNMR(CDCl3)δ3.12(s,3H),3.19(s,3H),3.80(s,6H),5.18(s,2H),6 92(s,1H),6.95(s,1H),7.12(d,J=8.7Hz,1H),7.32-7.51(m,8H),7.60-7.65(m,3H)IR(KBr)1491,1363,1210,1174,1151,1114cm-1 |
I-70 | m.p.109-110℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.19(s,3H),3.23(s,3H),3.80(s,6H),4.64(d,J=6.6Hz,2H),5.05-5.30(m,1H),6.92(s,1H),6.95(s,1H),7.06(d,J=8.7Hz,1H),7.33-7.37(m,2H),7.49(dd,J=2.1and8.7Hz,1H)7.58(d,J=2.1Hz,1H),7.61-7.64(m,2H)IR(KBr)1522,1489,1368,1351,1294,1260,1212,1178,1149,1114,975cm-1 |
I-71 | 1HNMR(CDCl3)δ1.72(s,3H),1.76(s,3H),3.72(s,3H),3.73(s,3H),4.56(d,J=6.6Hz,2H),5.46-5.49(brs,1H),6.79-6.82(m,2H),6.88-7.01(m,5H),7.34-7.39(m,2H),8.89(s,1H),9.45(s,1H)IR(KBr)3600-3100(br),1524,1493,1458,1386,1261,1206,1010cm-1 |
I-72 | m.p.123-124℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.19(s,3H),3.80(s,6H),4.64(d,J=6.9Hz,2H),5.52-5.57(m,1H),6.93(s,1H),6.94(s,1H),7.04(t,J=8.7Hz,1H),7.26-7.39(m,3H),7.60-7.65(m,2H)IR(KBr)1524,1494,1463,1379,1265,1211,1174,1154,1130cm-1 |
I-73 | m.p.118-119℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.79(s,3H),3.80(s,3H),4.63(d,J=6.9Hz,2H),4.86(s,1H),5.52-5.57(m,1H),6.88-6.93(m,4H),7.03(t,J=8.7Hz,1H),7.26-7.29(m,1H),7.37(dd,J=2.4and12.9Hz,1H),7.40-7.50(m,2H)IR(KBr)3600-3100(br),1525,1492,1466,1381,1263,1206cm-1 |
I-74 | 1HNMR(CDCl3)δ2.63(s,3H),3.19(s,3H),5.18(s,2H),5.74(s,1H),7.03(d,J=8.4Hz,1H),7.07(dd,J=2.1and8.4Hz,1H),7.12(d,J=2.1Hz,1H),7.36-7.68(m,12H)IR(KBr)3700-3200(br),1486,1367,1353,1197,1179,1147cm-1 |
I-75 | 1HNMR(CDCl3)δ2.80(s,3H),3.14(s,3H),3.19(s,3H),5.20(s,2H),7.18(d,J=8.4Hz,1H),7.38-7.68(m,14H)IR(KBr)1485,1361,1186,1156,1107cm-1 |
I-76 | 1HNMR(CDCl3)δ1.78(s,3H),1.82(s,3H),2.81(s,3H),3.19(s,3H),3.26(s,3H),4.65(d,J=7.2Hz,1H),5.47-5.52(m,1H),7.11(d,J=8.7Hz,1H),7.37-7.67(m,9H)IR(KBr)1486,1365,1186,1154,1106,973,926,870,810cm-1 |
I-77 | m.p.174-176℃1HNMR(CDCl3)δ1.72(s,3H),1.76(s,3H),4.55(d,J=6.0Hz,2H),5.45-5.49(m,1H),6.82-7.43(m,10H),8.84(s,1H),9.45(s,1H),9.53(s,1H)IR(KBr)3600-3100(br),1610,1594,1532,1496,1444,1409,1305,1245,1209cm-1 |
I-78 | m.p.134-135℃1HNMR(CDCl3)δ3.78(s,3H),3.79(s,3H),5.17(s,2H),5.70(s,1H),6.91(s,1H),6.95(s,1H),6.99(d,J=8.4Hz,1H),7.07-7.14(m,3H),7.22(d,J=2.1Hz,1H),7.36-7.47(m,5H),7.52-7.57(m,2H)IR(KBr)3600-3100(br),1524,1494,1462,1381,1273,1248,1213cm-1 |
I-79 | 1HNMR(CDCl3)δ3.12(s,3H),3.79(s,3H),3.80(s,3H),5.18(s,2H),6.92(s,1H),6.94(s,1H),7.09-7.15(m,3H),7.38-7.56(m,8H),7.60(d,J=2.1Hz,1H)IR(KBr)1522,1493,1467,1387,1365,1279,1213,1112cm-1 |
I-80 | m.p.110-111℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.22(s,3H),3.78(s,3H),3.80(s,3H),4.63(d,J=6.9Hz,2H),5.50-5.57(m,1H),6.91(s,1H),6.94(s,1H),7.04-7.14(m,3H),7.47-7.58(m,4H)IR(KBr)1552,1493,1364,1212,1110,970cm-1 |
I-81 | 1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.78(s,3H),3.79(s,3H),4.62(d,J=6.9Hz,2H),5.50-5.55(m,1H),5.72(s,1H),6.91-6.95(m,3H),7.06-7.14(m,3H),7.20(d,J=1.8Hz,1H),7.52-7.57(m,2H)IR(KBr)3536,1520,1493,1386,1271,1241,1210cm-1 |
I-82 | 1HNMR(CDCl3)δ1.29(t,J=7.2Hz,3H),1.76(s,3H),1.79(s,3H),3.78(s,6H),3.78(q,2H),4.64(d,J=6.3Hz,2H),4.72(s,2H),5.53-5.78(m,1H),6.61(s,1H),6.94(s,1H),6.98(d,J=8.7Hz,1H),7.09-7.20(m,4H),7.52-7.57(m,2H)IR(KBr)1758,1524,1496,1461,1387,1263,1209,1147cm-1 |
I-83 | 1HNMR(CDCl3)δ2.76(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),5.26(s,2H),6.85(s,1H),7.17(d,J=8.7Hz,1H),7.31-7.50(m,8H),7.60-7.71(m,3H),7.92(s,1H)IR(KBr)1684,1606,1512,1478,1177,1150,1080,1016cm-1 |
I-84 | 1HNMR(CDCl3)δ1.26(t,J=7.2Hz,3H),3.08(s,3H),3.22(s,3H),3.31(s,3H),3.74(s,3H),4.16(q,J=7.2Hz,2H),5.17(s,2H),6.44(d,J=16.5Hz,1H),6.89(s,1H),7.13(s,2H),7.27(d,J=8.4Hz,1H),7.35-7.50(m,8H),7.69(d,J=8.4Hz,2H)IR(KBr)1708,1633,1513,1465,1367,1271,1230,1176,1151,1120,1017cm-1 |
I-85 | 1HNMR(CDCl3)δ1.26(t,J=7.2Hz,3H),3.22(s,3H),3.31(s,3H),3.74(s,3H),4.16(q,J=7.2Hz,2H),5.15(s,2H),5.70(s,1H),6.53(d,J=16.5Hz,1H),6.69(dd,J=8.4and2.4Hz,1H),6.88(s,2H),7.00(d,J=8.4Hz,1H),7.33-7.50(m,8H),7.70(d,J=8.4Hz,2H)IR(KBr)3398,1675,1627,1581,1512,1465,1370,1284,1256,1221,1148,1074,1017cm-1 |
I-86 | 1HNMR(CDCl3)δ2.53(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),4.58(s,2H),5.24(s,2H),6.83(s,1H),6.96(d,J=8.4Hz,1H),7.28-7.57(m,9H),7.69(d,J=8.4Hz,2H)IR(KBr)1605,1512,1479,1366,1233,1175,1149,1080,1015cm-1 |
I-87 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.27(s,3H),3.78(s,3H),3.79(s,3H),4.63(d,J=6.6Hz,2H),5.40-5.50(m,1H),5.71(s,1H),6.07(s,1H),6.91-6.95(m,3H),7.05-7.20(m,3H),7.43-7.51(m,2H)IR(KBr)3600-3200(br),1617,1525,1494,1464,1361,1292,1208,1178,1101,1033cm-1 |
I-88 | 1HNMR(CDCl3)δ2.57(s,3H),3.20(s,3H),3.56(s,3H),3.79(s,3H),5.18(s,2H),6.84(s,1H),7.06-7.15(m,1H),7.20-7.40(m,9H),7.47-7.57(m,2H),7.60-7.75(m,3H),8.20-8.25(m,2H) |
I-89 | 1HNMR(CDCl3)δ3.44(s,3H),3.75(s,3H),5.01(s,1H),5.18(s,2H),6.01(s,1H),6.45(s,1H),6.88-6.97(m,2H),7.07(dd,J=8.4and8.4Hz,1H),7.15-7.21(m,1H),7.27(dd,J=12.3and2.1Hz,1H),7.29-7.43(m,3H),7.45-7.56(m,4H) |
I-90 | 1HNMR(CDCl3)δ1.68(s,3H),1.75(d,J=0.9Hz,3H),2.55(dt,J=6.9and6.9Hz,2H),2.70(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),4.04(t,J=6.9Hz,2H),5.17-5.28(m,1H),684(s,1H),7.04(dd,J=8.4and8.4Hz,1H),7.11-7.22(m,2H),7.34-7.42(m,2H),7.65-7.75(m,2H)IR(KBr)1522,1483,1361,1352,1176,1156,1079,963,873,801cm-1 |
I-91 | 1HNMR(CDCl3)δ2.96(s,3H),3.52(s,3H),3.58(s,6H),3.73(s,3H),4.89(s,2H),5.19(s,2H),5.23(s,2H),5.25(s,2H),6.68(s,1H),6.98(d,J=8.4Hz,1H),7.04(dd,J=8.4and2.1Hz,1H),7.11(m,2H),7.25(d,J=2.1Hz,1H),7.30-7.40(m,5H),7.51(m,2H)IR(KBr)2952,2935,2896,1609,1521,1477,1463,1438,1383,1269,1249,1228,1183,1153,1130,1116,1078,1066,1020,1008,984,944,922,903,832,801,730cm-1 |
I-92 | mp122-124℃1HNMR(CDCl3)δ2.70(brs,3H),3.55-3.60(br,2H),3.60(s,3H),3.75(s,3H),3.81-3.83(m,2H),3.87(s,3H),5.15(s,2H),5.68(s,1H),6.69(s,1H),6.94(dd,J=2.1,8.4Hz,1H),6.97-7.03(m,3H),7.07(d,J=1.8Hz,1H),7.38-7.48(m,5H),7.51-7.56(m,2H)IR(KBr)3600-2800(br),1607,1597,1550,1518,1477,1462,1452,1392,1289,1248,1228,1175,1122,1096,1084,1015cm-1 |
I-93 | 1HNMR(CDCl3)δ2.59(dt,J=6.6,6.6Hz,2H),3.45(s,3H),3.74(s,3H),4.15(t,J=6.6Hz,2H),5.15(dm,J=10.2Hz,1H),5.21(dm,J=17.1Hz,1H),5.90(m,1H),6.45(s,1H),6.92(d,J=8.4Hz,2H),6.95(s,2H),7.06(brs,1H),7.53(d,J=8.4Hz,2H)IR(Nujol)3570,3525,3336,3205,1616,1596,1524,1493,1409,1315,1286,1264,1239,1225,1117,1072,821,783cm-1 |
I-94 | 1HNMR(CDCl3)δ0.36(m,2H),0.66(m,2H),1.31(m,1H),3.45(s,3H),3.74(s,3H),3.91(d,J=7.2Hz,2H),6.44(s,1H),6.91(d,J=8.7Hz,2H),6.93(m,2H),7.07(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3570,3491,3364,3178,1617,1598,1583,1524,1494,1408,1313,1285,1266,1240,1224,1115,1072,1011,822,786cm-1 |
I-95 | 1HNMR(CDCl3)δ1.86(s,3H),3.45(s,3H),3.74(s,3H),4.54(s,2H),5.04(brs,1H),5.12(brs,1H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.95(m,2H),7.08(brs,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3536,3364,3179,1614,1586,1524,1493,1407,1309,1284,1265,1238,1226,1115,1073,1011,887,821,782cm-1 |
I-96 | 1HNMR(CDCl3)δ2.58(t,J=2.4Hz,1H),3.45(s,3H),3.74(s,3H),4.79(d,J=2.4Hz,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.98(dd,J=8.4,2.1Hz,1H),7.07(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3410,3282,1612,1589,1523,1489,1404,1226,1114,1071,1015,826cm-1 |
I-97 | 1HNMR(CDCl3)δ2.71(s,3H),3.21(s,3H),3.38(s,3H),3.56(s,3H),3.78(s,3H),5.47(s,2H),6.84(s,1H),7.00(d,J=8.6Hz,1H),7.34(dd,J=8.6,2.0Hz,1H),7.38(d,J=8.8Hz,2H),7.46(d,J=2.0Hz,1H),7.55(m,2H),7.67(m,1H),7.68(d,J=8.8Hz,2H),7.99(m,2H) |
I-98 | m.p.200-203℃1HNMR(CDCl3)δ2.38(s,3H),2.67(s,3H),3.12(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),5.14(s,2H),6.84(s,1H),7.15(d,J=8.7Hz,1H),7.21(d,J=8.1Hz,2H),7.34(d,J=8.1Hz,2H),7.34(dd,J=8.7,2.4Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.4Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1608,1520,1480,1359,1173,1156,1078,1016,976,948,872,818,791cm-1 |
I-99 | 1HNMR(CDCl3)δ2.72(s,3H),3.13(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.15(s,2H),6.84(s,1H),7.09(d,J=8.7Hz,1H),7.12(dd,J=8.7,7.2Hz,1H),7.35(dd,J=8.7,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.45(dd,J=8.7,5.1Hz,1H),7.68(d,J=8.7Hz,2H) |
I-100 | 1HNMR(CDCl3)δ2.76(s,3H),3.19(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.25(s,2H),6.85(s,1H),7.13(d,J=8.4Hz,1H),7.32(dd,J=8.4,1.8Hz,1H),7.36(dd,J=8.4,1.8Hz,1H),7.38(d,J=8.7Hz,2H),7.42(d,J=1.8Hz,1H),7.45(d,J=1.8Hz,1H),7.59(d,J=8.4Hz,1H),7.68(d,J=8.7Hz,2H) |
I-101 | m.p.103-105℃1HNMR(CDCl3)δ2.18(dd,J=1.5,1.2Hz,3H),3.45(s,3H),3.74(s,3H),4.79(dd,J=5.7,1.2Hz,2H),5.81(dt,J=5.7,1.5Hz,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.95(s,1H),6.96(s,1H),7.07(s,1H),7.52(d,J=8.7Hz,2H)IR(KBr)3527,3328,2930,1614,1593,1523,1492,1463,1408,1262,1235,1225,1119,1072,1010,828,805cm-1 |
I-102 | m.p.95-99℃1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),4.67(s,2H),5.47(m,1H),5.55(dd,J=2.7,1.2Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),7.01(m,2H),7.04(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H) |
I-103 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.59(d,J=4.2Hz,2H),6.45(s,1H),6.45(m,1H),6.55(d,J=12.9Hz,1H),6.92(d,J=8.7Hz,2H),6.96(brs,2H),7.08(brs,1H),7.53(d,J=8.7Hz,2H) |
I-104 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.64(dd,J=6.0and1.2Hz,2H),6.23(dt,J=13.2and6.0Hz,1H),6.42(dt,J=13.2and1.2Hz,1H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.96(brs,2H),7.08(brs,1H),7.58(d,J=8.7Hz,2H) |
I-105 | 1HNMR(CDCl3)δ3.46(s,3H),3.75(s,3H),3.98(d-like,J=7.2Hz,1H),4.64(d-like,J=3.9Hz,1H),6.04(dt,J=15.3,4.8Hz,1H),6.06(1H,dt,J=15.3,6.0Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.95(s,1H),7.08(s,2H),7.53(d,J=8.7Hz,2H) |
I-106 | 泡沫1HNMR(CDCl3)δ1.76(s,3H),1.83(s,3H),2.08(s,3H),3.36(s,3H),3.71(s,3H),4.61(d,J=7.0Hz,2H,),4.94(s,1H),5.54(t,J=7.0Hz,1H),5.70(s,1H),6.70(dd,J=8.4,2.0Hz,1H),6.74(s,1H),6.84(d,J=2.0Hz,1H)R(KBr)3410,1520,1476,1390,1243,1225,1101,1084,834,812,775cm-1 |
I-107 | m.p.112.114℃1HNMR(CDCl3)δ3.03(s,3H),3.57(s,3H),3.74(s,3H),3.87(s,3H),4.90(S,2H),5.15(s,2H),5.63(brs,1H),6.68(s,1H),6.91-7.07(m,5H),7.38-7.51(m,5H),7.53(m,2H)IR(KBr)3512,2952,2936,1607,1519,1468,1442,1382,1284,1253,1229,1215,1185,1156,1112,1079,1065,1020,983,956,914,831cm-1 |
I-108 | 1HNMR(CDCl3)δ2.20(d,J=1.2Hz,3H),2.76(s,3H),3.22(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.65(m,2H),5.96(m,1H),7.07(d,J=8.4Hz,1H),7.34-7.41(m,4H),7.68(m,2H) |
I-109 | m.p.153-154℃1HNMR(CDCl3)δ2.20(d,J=1.5Hz,3H),2.75(s,3H),3.21(s,3H),3.23(s,3H),3.56(s,3H),3.78(s,3H),4.81(m,2H),5.80(m,1H),6.84(s,1H),7.10(d,J=8.1Hz,1H),7.34-7.41(m,4H),7.68(m,2H)IR(KBr)1519,1481,1390,1364,1234,1177,1150,1119,1077,1011,969,945,876,816,799,521cm-1 |
I-110 | 1HNMR(CDCl3)δ2.68(s,3H),3.11(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),3.83(s,3H),5.11(s,2H),6.84(s,1H),6.93(d,J=8.7Hz,2H),7.16(d,J=8.7Hz,1H),7.35(dd,J=8.7,2.1Hz,1H),7.36-7.40(m,5H),7.68(d,J=8.7Hz,2H) |
I-111 | 1HNMR(CDCl3)δ2.78(s,3H),3.22(s,6H),3.55(s,3H),3.78(s,3H),5.23(s,2H),6.85(s,1H),7.08(d,J=8.7Hz,1H),7.34(dd,J=8.7,2.1Hz,1H),7.39(d,J=8.7Hz,2H),7.42(d,J=2.1Hz,1H),7.44(brs,2H),7.68(d,J=8.7Hz,2H),8.70(brs,2H) |
I-112 | 1HNMR(CDCl3)δ2.70(s,3H),3.21(s,3H),3.24(s,3H),3.55(s,3H),3.78(s,3H),5.33(s,2H),6.84(s,1H),7.15(d,J=8.4Hz,1H),7.27(dd,J=7.5,4.2Hz,1H),7.33(dd,J=8.4,2.4Hz,1H),7.38(d,J=8.7Hz,2H),7.42(d,J=2.4Hz,1H),7.62(brd,J=7.5Hz,1H),7.68(d,J=8.7Hz,2H),7.76(ddd,J=7.5,7.5,1.8Hz,1H),8.6(d,J=4.2Hz,1H) |
I-113 | 1HNMR(CDCl3)δ2.76(s,3H),3.15(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.22(s,2H),6.85(s,1H),7.17(d,J=8.4Hz,1H),7.38(dd,J=8.4,2.1Hz,1H),7.38(m,1H),7.39(d,J=8.7Hz,2H),7.42(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H),7.88(d,J=7.8Hz,1H),7.64(brs,1H),8.73(brs,1H) |
I-114 | 1HNMR(CDCI3)δ3.45(s,3H),3.74(s,3H),5.10(s,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.95(dd,J=8.4,2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.23(brd,J=7.8Hz,2H),7.34(brd,J=7.8Hz,2H),7.53(d,J=8.7Hz,2H)IR(Nujol)3464,3344,1611,1581,1523,1490,1266,1113,1073,1011,1000,821,782cm-1 |
I-115 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.11(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.96(dd,J=8.4,2.1Hz,1H),7.01(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.11(dd,J=8.7,8.7Hz,2H),7.42(dd,J=8.7,5.4Hz,2H),7.54(d,J=8.7Hz,2H)IR(Nujol)3560,3400,1612,1589,1522,1492,1260.1225,1116,1068,1006,992,841,826,803,786cm-1 |
I-116 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.23(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.97(brs,2H),7.11(brs,1H),7.31(dd,J=8.4,2.1Hz,1H),7.46(d,J=8.4Hz,1H),7.47(d,J=2.1Hz,1H),7.54(d,J=8.7Hz,2H)IR(Nujol)3460,3359,1610,1594,1522,1490,1264,1164,1110,1072,1008,877,824,781cm-1 |
I-117 | 1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),3.84(s,3H),5.07(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.95(d,J=9.0Hz,2H),6.96(dd,J=8.4,1.8Hz,1H),7.04(d,J=8.4Hz,1H),7.08(d,J=1.8Hz,1H),7.37(d,J=8.7Hz,2H),7.53(d,J=9.0Hz,2H)IR(Nujol)3400,1612,1586,1516,1188,1246,1174,1113,1070,1011,823cm-1 |
1-118 | 1HNMR(DMSO-d6)δ3.29(s,3H),3.64(s,3H),5.20(s,2H),6.39(s,1H),6.64(dd,J=8.4,2.1Hz,1H),6.79(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),6.92(d,J=8.4Hz,1H),7.43(d,J=8.7Hz,2H),7.52(d,J=6.0Hz,2H),8.69(d,J=6.0Hz,2H)IR(Nujol)3473,3441,1610,1582,1523,1493,1404,1241,1112,1074,1005,816,782cm-1 |
I-119 | 1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),5.27(s,2H),6.45(s,1H),6.92(dd,J=8.4,1.8Hz,1H),6.93(d,J=8.7Hz,2H),7.11(d,J=8.4Hz,1H),7.12(d,J=1.8Hz,1H),7.31(m,1H),7.36(brd,J=7.5Hz,1H),7.53(d,J=8.7Hz,2H),7.77(ddd,J=7.5,7.5,1.8Hz,1H),8.66(d,J=5.0Hz,1H)IR(Nujol)3555,3467,3342,1608,1597,1586,1522,1466,1210,1117,1080,1016,822,761cm-1 |
I-120 | 1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),5.21(s,2H),6 46(s,1H),6.91(d,J=8.7Hz,2H),6.99(brs,2H),7.11(brs,1H),7.40(dd,J=7.5,5.0Hz,1H),7.53(d,J=8.7Hz,2H),7.83(d,J=7.5Hz,1H),8.64(brd,J=5.0Hz,1H),8.74(brs,1H)IR(Nujol)3342,1609,1586,1522,1489,1253,1118,1074,1010,827,782cm-1 |
I-121 | m.p.166-168℃1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.77(d,J=6.3Hz,2H),6.22(t,J=6.3Hz,1H),6.93(d,J=8.7Hz,2H),6.93(d,J=8.7Hz,1H),6.98(dd,J=8.7,1.8Hz,1H),7.08(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3474,3411,2957,2930,1615,1589,1569,1523,1492,1407,1286,1263,1230,1113,1070,825cm-1 |
I-122 | m.p.190-192℃1HNMR(CDCl3)δ2.56(s,3H),3.22(s,3H),3.56(s,3H),3.79(s,3H),5.17(s,2H),5.73(s,1H),6.84(s,1H),6.93(dd,J=8.1and1.9Hz,1H),7.02(d,J=8.1Hz,1H),7.05(d,J=1.9Hz,1H),7.37-7.45(m,1H),7.71(d,J=8.6Hz,2H)IR(KBr)3512,1519,1484,1367,1174,1150,1078,957,870,798cm-1 |
I-123 | 泡沫1HNMR(CDCl3)δ3.08(s,3H),3.21(s,3H),3.44(s,3H),3.78(s,3H),5.15(s,2H),6.95(s,1H),7.11(d,J=8.7Hz,1H),7.33-7.47(m,9H),7.71(d,J=8.7Hz,2H),13.3-14.5(brs,1H)IR(KBr):3422,1735,1702,1520,1471,1366,1175,1150,1118,971,954,863,807cm-1 |
I-124 | m.p.258-259℃(dec)1HNMR(DMSO-d6)δ3.32(s,3H),3.69(s,3H),5.10(2H,s),6.65(dd,J=8.4,2.1Hz,1H),6.79(d,J=2.1Hz,1H),6.86(d,J=8.4Hz,2H),6.90(s,1H),6.94(d,J=8.4Hz,1H),7.30-7.54(m,7H),8.98(s,1H),9.63(s,1H)IR(KBr):3437,3157,1702,1610,1590,1521,1474,1464,1379,1260,1245,1224,1061,1014,952,834,793,748,698cm-1 |
I-125 | 1HNMR(CDCl3)δ1.75(s,3H),1.81(s,3H),3.21(s,3H),3.41(s,3H),3.68(s,3H),3.77(s,3H),4.61(d,J=6.8Hz,2H),5.50(t,J=6.8Hz,1H),6.93(s,1H),7.02(d,J=8.5Hz,1H),7.27(d,J=8.5,2.3Hz,1H),7.33(dd,J=2.3Hz,1H),7.38(d,J=8.6Hz,2H),7.71(d,J=8.6Hz,2H) |
I-126 | 1HNMR(CDCl3)δ1.75(s,3H),1.81(s,3H),3.41(s,3H),3.65(s,3H),3.76(s,3H),4.59(d,J=6.6Hz,2H),5.06(s,1H),5.51(t,J=6.6Hz,1H),5.67(s,1H),6.83(dd,J=8.4,2.1Hz,1H),6.87(s,1H),6.90-6.93(m,3H),6.98(d,J=2.1Hz,1H),7.54(d,J=9.0Hz,2H) |
I-127 | m.p.116-117℃1HNMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),3.32(s,3H),3.70(s,3H),4.53(d,J=7.1Hz,2H),5.48(t,J=7.1Hz,1H),6.65(dd,J=8.4,2.1Hz,1H),6.73(d,J=2.1Hz,1H),6.86(d,J=8.6Hz,2H),6.88(d,J=8.4Hz,1H),6.93(s,1H),7.47(d,J=8.6Hz,2H),8.84(s,1H),9.62(s,1H),11.9-13.4(brs,1H)IR(KBr):3446,1703,1611,1593,1520,1471,1380,1260,1225,1081,997,952,838cm-1 |
I-128 | 油状物1HNMR(CDCl3)δ1.65(s,3H),1.78(s,3H),2.96(s,3H),3.22(s,3H),3.25(s,3H)3.55(s,3H),3.79(s,3H),4.77(d,J=7.8Hz,2H),5.53(t,J=7.8Hz,1H),6.87(s,1H),7.39&7.67(ABq,J=8.7Hz,4H),7.70(d,J=2.1Hz,1H),7.86(d,J=2.1Hz,1H),10.36(s,1H)IR(CHCl3)1691,1473,1374,1230,1226,1209,1178,1152,1086,969,874,805cm-1 |
I-129 | 油状物1HNMR(CDCl3)δ1.73(d,J=0.9Hz,3H),1.80(s,3H),2.89(s,3H),3.20(s,3H),3.22(s,3H),3.54(s,3H),3.79(s,3H),4.66(d,J=7.8Hz,2H),4.77(s,2H),5.55(m,1H),6.85(s,1H),7 39&7 .68(ABq,J=9.0Hz,4H),7.39(d,J=2.1Hz,1H),7.44(d,J=2.1Hz,1H)IR(CHCl3)1475,1372,1230,1178,1151,1085,969,874cm-1 |
I-130 | m.p.189-190℃1HNMR(CDCl3)δ1.36(s,9H),2.81(s,3H),3.22(s,3H),3.30(s,3H),3.56(s,3H),3.79(s,3H),6.86(s,1H),7.36-7.42(m,3H),7.54(d,J=1.8Hz,1H),7.67-7.72(m,3H)IR(KBr)1472,1363,1331,1179,1153,1082,961,950,877,846,817,791,526cm-1 |
I-131 | m.p.147-148℃1HNMR(CDCl3)δ2.95(s,3H),3.18(s,3H),3.22(s,3H),3.55(s,3H),3.79(s,3H),5.28(s,2H),6.86(s,1H),7.38-7.44(m,7H),7.67(m,2H),7.75(d,J=2.1Hz,1H),7.83(d,J=2.1Hz,1H)IR(KBr)1687,1512,1472,1365,1352,1234,1201,1180,1151,1082,971,947,870,846,810,794,703,523cm-1 |
I-132 | m.p.122-124℃1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.80(s,3H),3.22(s,3H),3.28(s,3H),3.56(s,3H),3.62(d,J=7.8Hz,2H),3.78(s,3H),5.31(m,1H),6.85(s,1H),7.34(dd,J=8.1Hz,J=1.8Hz,1H),7.39&7.68(ABq,J=8.7Hz,4H),7.43(d,J=8.1Hz,1H),7.46(d,J=1.8Hz,1H)IR(KBr)1474,1362,1180,1151,1076,1014,968,944,870,816,799,521cm-1 |
I-133 | 1HNMR(CDCl3)δ1.73(d,J=0.9Hz,3H),1.82(s,3H),3.44(s,3H),3.75(s,3H),4.54(d,J=6.9Hz,2H),4.78(s,2H),5.30(s,1H),5.61(m,1H),5.67(s,1H),6.01(s,1H),6.45(s,1H),6.92&7.52(ABq,J=8.7Hz,4H),7.02(d,J=2.1Hz,1H),7.05(d,J=2.1Hz,1H)IR(KBr)3428,1612,1522,1483,1458,1403,1362,1334,1304,1266,1226,1174,1116,1083,1024,970,938cm-1 |
I-134 | m.p.167-168℃1HNMR(CDCl3)δ1.39(d,J=1.2Hz,3H),1.70(s,3H),3.36(d,J=8.1Hz,2H),3.45(s,3H),3.74(s,3H),4.98(s,1H),5.29(m,1H),5.96(s,1H),6.45(s,1H),6.78(s,1H),6.93&7.54(ABq,J=8.7Hz,4H),6.96(dd,J=7.8Hz,J=1.8Hz,1H),7.09(d,J=1.8Hz,1H),7.49(d,J=7.8Hz,1H)1R(KBr)3413,3365,2931,1611,1552,1520,1502,1475,1455,1441,1402,1360,1323,1262,1227,1206,1182,1170,1162,1114,1100,1081,1052,1014,941,835,816,587,542cm-1 |
I-135 | m.p.183-184℃1HNMR(CDCl3)δ3.46(s,3H),3.74(s,3H),3.83(s,3H),4.78(m,2H),5.99(m,1H),6.44(m,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.94(dd,J=8.1,1.8Hz,1H),7.00(d,J=8.1Hz,1H),7.10(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3383,2929,1699,1523,1491,1405,1262,1236,1206,1173,1116,1071,1011,822cm-1 |
I-136 | 1HNMR(CD3OD)δ1.26(s,3H),1.29(s,3H),3.38(s,3H),3.68(s,3H),3.80(dd,J=8.4,2.7Hz,1H),3.96(dd,J=9.6,8.4Hz,1H),4.34(dd,J=9.6,2.7Hz,1H),6.44(s,1H),6.80(dd,J=8.1,1.8Hz,1H),6.85(d,J=8.7Hz,2H),6.86(d,J=1.8Hz,1H),7.96(d,J=8.1Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3367,1612,1588,1523,1489,1254,1226,1115,1072,1013,940,814cm-1 |
I-137 | 1HNMR(CD3OD)δ3.38(s,3H),3.68(s,3H),4.02(dd,J=11.0,3.6Hz,1H),4.12(dd,J=11.0,1.8Hz,1H),5.48(dd,J=3.6,1.8Hz,1H),6.43(s,1H),6.83-6.87(m,3H),6.85(d,J=8.7Hz,2H),7.46(d,J=8.7Hz,2H)IR(Nujol)3410,1612,1588,1522,1487,1269,1231,1114,1071,1011,947,824cm-1 |
I-138 | 1HNMR(CD3OD)δ3.38(s,3H),3.68(s,3H),4.70(d,J=5.4Hz,2H),6.43(s,1H),6.80(dd,J=8.1,2.1Hz,1H),6.85(d,J=8.4Hz,2H),6.88(d,J=2.1Hz,1H),6.98(d,J=8.1Hz,1H),7.46(d,J=8.4Hz,2H),7.62(t,J=5.4Hz,1H)IR(Nujol)3368,1612,1589,1523,1589,1253,1226,1114,1072,1011,940,825cm-1 |
I-139 | 1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),3.92(s,3H),4.75(d,J=5.1Hz,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.92(d,J=6.0Hz,1H),7.00(dd,J=6.0,1.8Hz,1H),7.09(d,J=1.8Hz,1H),7.52(d,J=8.7Hz,2H),7.58(t,J=5.1Hz,1H)IR(Nujol)3399,1612,1589,1523,1489,1252,1226,1115,1072,1043,1014,941,825cm-1 |
I-140 | 1HNMR(CD3OD)δ3.38(s,3H),3.68(s,3H),4.51(s,2H),4.71(d,J=5.4Hz,2H),643(s,1H),6.80(dd,J=8.4,2.1Hz,1H),6.85(d,J=8.4Hz,2H),6.87(d,J=2.1Hz,1H),6.98(d,J=8.4Hz,1H),7.46(d,J=8.4Hz,2H),7.75(t,J=5.4Hz,1H)IR(Nujol)3384,1611,1588,1523,1489,1252,1227,1115,1072,1014,824,758cm-1 |
I-141 | 1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),4.76(d,J=5.1Hz,2H),5.15(s,2H),6.45(s,1H),6.86(d,J=8.4Hz,1H),6.92(d,J=8.7Hz,2H),6.94(dd,J=8.4,2.1Hz,1H),7.08(d,J=2.1Hz,1H),7.31-7.40(m,5H),7.53(d,J=8.7Hz,2H),7 65(t,J=5.1Hz,1H)IR(Nujol)3399,1611,1588,1523,1489,1251,1225,1115,1072,1013,940,825cm-1 |
I-142 | 1HNMR(CDCl3-CD3OD1∶1)δ3.26(s,3H),2.64(m,4H),3.13(m,4H),3.44(s,3H),3.73(s,3H),4.78(d,J=4.5Hz,2H),6.45(s,1H),6.90(d,J=8.7Hz,2H),6.90(dd,J=8.4,2.1Hz,1H),6.99(d,J=2.1Hz,1H),7.00(d,J=8.4Hz,1H),7.12(t,J=4.5Hz,1H),7.49(d,J=8.7Hz,2H)IR(Nujol)3492,3297,1607,1561,1523,1486,1247,1224,1113,1011,957,828,799cm-1 |
I-143 | 1HNMR(CDCl3)δ3.09(m,4H),3.45(s,3H),3.74(s,3H),3.86(m,4H),4.82(d,J=4.2Hz,2H),6.44(s,1H),6.92(d,J=8.7Hz,2H),6.98(dd,J=8.4,1.8Hz,1H),7.00(t,J=4 2Hz,1H),7.04(d,J=8.4Hz,1H),7.07(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3366,1611,1586,1523,1488,1268,1227,1114,1070,1011,823cm-1 |
I-144 | 1HNMR(CDCl3)δ1.29(t,J=6.9Hz,3H),2.65(dd,J=15.9,6.6Hz,1H),2.81(dd,J=15.9,6.6Hz,1H),3.44(s,3H),3.75(s,3H),4.03(dd,J=11.4,6.9Hz,1H),4.20(q,J=6.9Hz,2H),4.35(dd,J=11.4,2.4Hz,1H),4.66(ddt,J=6.9,6.6,2.4Hz,1H),6.44(s,1H),6.92(d,J=8.7Hz,2H),6.96-7.01(m,3H),7.53(d,J=8.7Hz,2H) |
I-145 | 油状物1HNMR(CDCl3)δ1.68(s,3H),1.74(d,J=0.9Hz,3H),2.55(m,2H),3.44(s,3H),3.75(s,3H),4.04(t,J=7.2Hz,2H),4.97(brs,1H),5.23(m,1H),6.00(s,1H),6.45(s,1H),6.92&7.53(ABq,J=8.7Hz,4H),7.02(m,1H),7.17-7.22(m,2H)IR(KBr)1613,1525,1490,1475,1463,1454,1402,1304,1269,1231,1112,1072,1019,827cm-1 |
I-146 | m.p.256-257℃1HNMR(DMSO-d6)δ3.35(s,3H),3.44(s,3H),3.74(s,3H),5.22(s,2H),7.06(s,1H),7.28-7.56(m,11H),7.69(s,1H),7.76(d,J=8.6Hz,2H)IR(KBr):3479,3360,1672,1517,1465,1361,1339,1295,1261,1228,1172,1144,1118,1013,957,870,852,804,751cm-1 |
I-147 | m.p.163-164℃1HNMR(CDCl3)δ1.74(s,3H),1.81(s,3H),3.43(s,3H),3.74(s,3H),4.58(d,J=6.8Hz,2H),5.50(t,J=6.8Hz,1H),5.80(s,1H),6.37(s,1H),6.86-6.95(m,5H),6.90(d,J=8.6Hz,2H),6.99(s,1H),7.49(d,J=8.6Hz,2H)IR(KBr):3533,3412,3350,1655,1609,1588,1519,1469,1373,1274,1245,1227,1131,1082,1060,999,954,838cm-1 |
I-148 | 1HNMR(CDCl3)δ2.88(s,3H),3.22(s,3H),3.54(s,3H),3.77(s,3H),5.35(m,2H),6.85(s,1H),7.24(d,J=9.0Hz,1H),7.39(d,J=8.7Hz,2H),7.42-7.46(m,5H),7.65(d.d,J=9.0&2.1Hz,1H),7.68(d,J=8.7Hz,2H),8.26(d,J=2.1Hz,1H) |
I-149 | 1HNMR(CDCl3)δ1.80(s,3H),1.85(s,3H),3.43(s,3H),3.74(s,3H),4.80(d,J=6.9Hz,2H),5.76(t,J=6.9Hz,1H),6.46(s,1H),6.92(d,J=8.4Hz,2H),7.14(d,J=8.7Hz,1H),7.49(d,J=8.4Hz,2H)7.70(d.d,J=8.7&2.1Hz,1H),8.28(d,J=2.1Hz,1H)IR(KBr)3472,1707,1671,1610,1520,1482,1460,1426,1269,1226,1119,1076,1012cm-1 |
I-150 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.63(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),4.62(d,J=6.3Hz,2H),4.73(s,2H),5.50(t,J=6.3Hz,H),6.84(s,1H),6.99(d,J=9.0Hz,1H),7.51-7.42(m,9H),7.70(d,J=9.0Hz,2H)IR(KBr)3432,1607,1512,1479,1364,1234,1176,1151,1079,1016cm-1 |
I-151 | 1HNMR(CDCl3)δ1.58(s,3H),1.81(s,3H),3.45(s,3H),3.73(s,3H),4.61(d,J=6.6Hz,2H),4.72(s,2H),5.52(t,J=6.6Hz,1H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.98(d,J=8.4Hz,1H),7.36(d.d,J=8.4&2.1Hz,1H),7.38(d,J=2.1Hz,1H),7.50(d,J=8.4Hz,2H)IR(KBr)3580,3411,1611,1521,1485,1464,1397,1233,1113,1077,1024,1001cm-1 |
I-152 | 1HNMR(CDCl3)δ3.50(s,3H),3.77(s,3H),5.15(s,2H),5.72(s,1H),6.03(s,2H),6.71(d.d,J=8.4&2.1Hz,1H),6.91(d,J=8.4Hz,1H),6.97(s,1H),6.98(d,J=8.4Hz,1H),7.07(s,1H),7.09(d.d,J=8.4&2.1Hz,1H),7.16(d,J=2.1Hz,1H),7.34-7.50(m,5H),989(s,1H)IR(KBr)3446,1697,1587,1511,1470,1383,1285,1240,1127,1036cm-1 |
I-153 | 1HNMR(CDCl3)δ3.78(s,3H),3.79(s,3H),4.87(s,1H),5.16(s,2H),5.70(s,1H),6.88-6.91(m,2H),6.97(s,1H),7.00(s,1H),6.99(d,J=8.4Hz,1H),7.08(dd,J=21,8.4Hz,1H),7.23(d,J=2.1Hz,1H),7.34-7.49(m,7H) |
I-154 | 1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.51-2.58(m,2H),3.19(s,3H),3.21(s,3H),3.79(s,3H),3.80(s,3H),4.07(t,J=6.9Hz,2H),6.18-5.27(m,1H),6.92(s,IH),6.95(s,1H),7.05(d,J=8.7Hz,1H),7.32-7.37(m,2H),7.49(dd,J=2.1,8.7Hz,1H),7.58(d,J=2.1Hz,1H),7.60-7.64(m,2H) |
I-155 | 1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.53(q,J=6.9Hz,2H),3.77(s,3H),3.78(s,3H),4.07(t,J=6.9Hz,2H),4.97(s,3H),5.20-5.25(m,1H),5.71(s,1H),6.87-6.93(m,3H),7.07(dd,J=1.8,8.4Hz,1H),7.20(d,J=1.8Hz,1H),7.45-7.50(m,2H) |
I-156 | m.p.163-175℃1HNMR(CDCl3)δ2.76(s,3H),3.19(s,3H),3.22(s,3H),3.54(s,3H),3.79(s,3H),5.20(s,2H),5.68(s,1H),6.84(s,1H),6.97(d,J=1.8Hz,1H),6.99(d,J=1.8Hz,1H),7.37-7.47(m,7H),7.68(m,2H)IR(KBr)3436,1480,1415,1391,1363,1233,1178,1151,1079,1024,969,953,875,801,522cm-1 |
I-157 | m.p.176-178℃1HNMR(CDCl3)δ2.08(s,3H),2.40,(s,3H),2.72(s,3H),3.21(s,3H),3.22(s,3H),3.55(s,3H),3.79(s,3H),5.13(s,2H),6.86(s,1H),7.39and7-68(ABq,J=8.7Hz,4H),7.47(d,J=2.1Hz,1H),7.49(d,J=2.1Hz,1H)IR(KBr)1770,17d7,1477,1391,1366,1235,1180,1152,1077,873,799,522cm-1 |
I-158 | m.p.175-177℃1HNMR(CDCl3)δ2.87(s,3H),3.13(s,6H),3.22(s,3H),3.55(s,3H),3.81(s,3H),5.22(s,2H),6.86(s,1H),7.38-7.45(m,7H),7.51-7.53(m,2H),7.67(m,2H)IR(KBr)1479,1367,1180,1151,1080,1019,966,876,798,525cm-1 |
I-159 | 泡沫1HNMR(CDCl3)δ2.44(s,3H),3.21(s,3H),3.54(s,3H),3.76(s,3H),3.79(s,3H),4.77(s,2H),5.24(s,2H),6.83(s,1H),6.90.7.00(m,3H),7.30-7.48(m,5H),7.37(d,J=8.8Hz,2H),7.69(d,J=8.8Hz,2H)IR(KBr):1758,1519,1481,1365,1236,1176,1150,1079,1013,963,872,798cm-1 |
I-160 | m.p.146-147℃1HNMR(DMSO-d6)δ3.31(s,3H),3.65(s,3H),4.63(s,2H),5.15(s,2H),6.40(s,1H),6.83-6.90(m,4H),7.05(d,J=8.4Hz,1H),7.32-7.52(m,7H),8.57(s,1H),9.50(s,1H),12.0-13.9(brs,1H)IR(KBr):3422,1728,1611,1524,1489,1455,1405,1247,1142,1118,1080,1012,818,749,742,698cm-1 |
I-161 | 1HNMR(CDCl3)δ1.76(s,3H),1.79(s,3H),2.57(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),3.80(s,3H),4.64(d,J=6.5Hz,2H),4.74(s,2H),5.54(t,J=6.5Hz,1H),6.83(s,1H),6.88(d,J=1.5Hz,1H),7.02-7.03(m,2H),7.38(d,J=8.7Hz,2H),7.69(d,J=8.7Hz,2H) |
I-162 | m.p.147-149℃1HNMR(DMSO-d6)δ1.73(s,3H),1.77(s,3H),3.30(s,3H),3.65(s,3H),4.57(d,J=6.6Hz,2H),4.60(s,2H),5.86(t,J=6.6Hz,1H),6.40(s,1H),6.80(d,J=1.7Hz,1H),6.84(d,J=8.7Hz,2H),6.87(dd,J=8.7Hz,1H),6.99(d,J=8 7Hz,1H),7.43(d,J=8.7Hz,2H),8.56(s,1H),9.51(s,1H),12.8 (brs,1H)IR(KBr):3483,3376,1737,1612,1523,1489,1460,1397,1271,1231,1175,1120,1072,1012,904,820cm-1 |
I-163 | m.p.144-145℃1HNMR(CDCl3)δ3.04(s,3H),3.20(s,3H),3.59(s,3H),3.75(s,3H),4.90(s,2H),5.16(s,2H),5.65(s,1H),6.67(s,1H),6.92(dd,J=2.1,8.4Hz,1H),7.00(d,J=8.4Hz,1H),7.06(d,J=2.1Hz,1H),7.26-7.47(m,7H),7.61-7.66(m,2H)IR(KBr)3600-3200(br),1517,1477,1449,1382,1361,1277,1235,1199,1150,1112,1079,1064,1010,997cm-1 |
I-164 | m.p.80-83℃1HNMR(CDCl3)δ2.99(s,3H),3.12(s,3H),3.20(s,3H),3.58(s,3H),3.75(s,3H),4.93(s,3H),5.18(s,2H),6.67(s,1H),7.12(d,J=8.7Hz,1H),7.34-7.49(m,9H),7.60-7.65(m,2H) |
I-165 | m.p.148-151℃1HNMR(CDCl3)δ3.03(s,3H),3.57(s,3H),3.74(s,3H),4.89(s,1H),4.90(s,2H),5.15(s,2H),5.64(s,1H),6.67(s,1H),6.88-6.93(m,3H),6.99(d,J=8.4Hz,1H),7.06(d,J=1.8Hz,1H),7.20-7.49(m,7H)IR(KBr)3600-3200(br),1609,1590,1519,1477,1459,1381,1253,1216,1156,1111,1077,1066,1012cm-1 |
I-166 | m.p.199℃1HNMR(CDCl3)δ310(s,3H),3.21(s,3H),3.44(s,3H),3.76(s,3H),5.17(s,2H),6.03(s,1H),6.44(s,1H),7.14(d,J=8.4Hz,1H),7.36-7.49(m,8H),7.52(d,J=2.1Hz,1H),7.67-7.72(m,2H)IR(KBr)3600-3200(br),1520,1486,1362,1183,1152,1110,971cm-1 |
I-167 | m.p.113-115℃1HNMR(CDCl3)δ0.76(t,J=7.2Hz,3H),1.46-1.55(m,2H),3.11(s,3H),3.20(s,1H),3.63(s,1H),3.71(t,J=6.6Hz,2H),5.18(s,2H),6.64(s,1H),7.11(d,J=8.7Hz,1H),7.33-7.50(m,9H),7.60-7.65(m,2H)IR(KBr)1517,1475,1365,1345,1293,1233,1177,1149,1109,1079,1017,956cm-1 |
I-168 | m.p.56-58℃1HNMR(CDCl3)δ0.76(t,J=7.5Hz,3H),1.441.56(m,2H),3.61(s,3H),3.71(t,J=6.6Hz,2H),3.74(s,3H),4.86(s,1H),5.15(s,2H),5.63(s,1H),6.65(s,1H),6.88-6.93(m,3H),6.98(d,J=8.4Hz,1H),7.04(d,J=1.8Hz,1H),7.37-7.50(m,7H)IR(KBr)3600-3200(br),1611,1590,1519,1476,1404,1379,1252,1230,1110,1078,1015cm-1 |
I-169 | m.p.101-103℃1HNMR(CDCl3)δ0.77(t,J=7.5Hz,3H),1.44-1.55(m,2H),1.76(s,3H),1.81(s,3H),3.20(s,3H),3.21(s,3H),3.63(s,3H),3.71(t,J=6.6Hz,2H),3.75(s,3H),4.63(d,J=6.6Hz,2H),5.48-5.53(m,1H),6.64(s,1H),7.04(d,J=8.4Hz,1H),7.32-7.38(m,3H),7.42(d,J=2.1Hz,1H),7.60-7.65(m,2H)IR(KBr)1514,1473,1370,1359,1290,1233,1174,1149,1107,970cm-1 |
I-170 | m.p.64-66℃1HNMR(CDCl3)δ0.77(t,J=7.5Hz,3H),1.44-1.55(m,2H),1.76(s,3H),1.81(s,3H),3.20(s,3H),3.21(s,3H),3.63(s,3H),3.71(t,J=6.6Hz,2H),3.75(s,3H),4.63(d,J=6.6Hz,2H),5.18-5.53(m,1H),6.64(s,1H),7.04(d,J=8.4Hz,1H),7.32-7.38(m,3H),7.42(d,J=2.1Hz,1H),7.60-7.65(m,2H)IR(KBr)3600-2800(br),1612,1590,1520,1475,1462,1405,1381,1285,1244,1226,1110,1079,988cm-1 |
I-171 | m.p.148-150℃1HNMR(CDCl3)δ1.74(d,J=0.9Hz,3H),1.80(s,3H),2.88(s,3H),3.22(s,3H),3.23(s,6H),3.55(s,3H),3.80(s,3H),4.72(d,J=7.5Hz,2H),5.55(m,1H),6.85(s,1H),7.39&7.67(ABq,J=8.7Hz,4H),7.40(s,2H)IR(KBr)1514,1479,1411,1366,1179,1152,1079,1022,968,875,799,525cm-1 |
I-172 | 1HNMR(CDCl3)δ0.94(t,J=7.2Hz,3H),1.45(tq,J=7.2,7.2Hz,2H),2.13(m,2H),3.46(s,3H),3.74(s,3H),4.68(d,J=5.4Hz,2H),5.72(m,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.96(brs,2H),7.07(brs,1H),7.53(d,J=8.7Hz,2H) |
I-173 | 1HNMR(CDCl3)δ1.76(brd,J=6.3Hz,3H),3.46(s,3H),3.74(s,3H),4.70(d,J=5.4Hz,2H),5.77(m,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.96(brs,2H),7.07(brs,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3350,1613,1587,1523,1491,1287,1261,1238,1114,1071,1011,936,820,783cm-1 |
I-174 | 1HNMR(CDCl3)δ3.45(s,3H),3.76(s,3H),4.56(s,2H),5.55(s,1H),6.45(s,1H),6.93(d,J=8.7Hz,2H),7.01(d,J=8.4Hz,1H),7.08(dd,J=8.4,2.1Hz,1H),7.27(d,J=2.1Hz,1H),7.54(d,J=8.7Hz,2H) |
I-175 | 1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),4.82(dd,J=6.6,1.5Hz,2H),5.28(d,J=10.5Hz,1H),5.35(d,J=16.5Hz,1H),5.75(dt,J=10.8,6.6Hz,1H),6.26(dd,J=10.5,10.5Hz,1H),6.45(s,1H),6.66(ddd,J=16.5,10.5,10.5Hz,1H),6.92(d,J=8.7Hz,2H),6.96(m,2H),7.07(brs,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3399,1611,1591,1523,1489,1248,1226,1113,1071,1009,825cm-1 |
I-176 | 1HNMR(CDCl3)δ1.59(m,6H),2.17(m,2H),2.24,(m,2H),2.71(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.65(d,J=7.2Hz,2H),5.43(t,J=7.2Hz,1H),6.84(s,1H),7.10(d,J=8.4Hz,1H),7.34(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.39(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H) |
I-177 | m.p.177-178℃1HNMR(CDCl3)δ2.31(t,J=5.7Hz,2H),2.39(t,J=5.7Hz,2H),2.76(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.70(t,J=5.7Hz,2H),3.73(t,J=5.7Hz,2H),3.78(s,3H),4.67(d,J=6.6Hz,2H),5.57(t,J=6.6Hz,1H),6.84(s,1H),7.09(d,J=8.4Hz,1H),7.35(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.39(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)2940,1519,1481,1362,1178,1152,1079,818cm-1 |
I-178 | 1HNMR(CDCl3)δ1.04(t,J=7.5Hz,3H),1.05(t,J=7.5Hz,3H),2.12(q,J=7.5Hz,2H),2.16(q,J=7.5Hz,2H),2.71(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.67(d,J=6.6Hz,2H),5.45(t,J=6.6Hz,1H),6.84(s,1H),7.11(d,J=8.4Hz,1H),7.35(dd,J=8.4,2.4Hz,1H),7.38(d,J=8.7Hz,2H),7.39(d,J=2.4Hz,1H),7.68(d,J=8.7Hz,2H) |
I-179 | 1HNMR(CDCl3)δ1.05(t,J=7.5Hz,3H),1.76(s,3H),2.10(q,J=7.5Hz,2H),2.71(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.66(d,J=6.9Hz,2H),5.48(t,J=6.9Hz,1H),6.84(s,1H),7.10(d,J=8.4Hz,1H),7.34(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.39(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H) |
I-180 | 1HNMR(CDCl3)δ1.76(s,3H),1.80(s,6H),2.72(s,3H),3.21(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),4.61(s,2H),6.84(s,1H),7.10(d,J=8.4Hz,1H),7.34(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.39(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H) |
I-181 | m.p.157-158℃1HNMR(CDCl3)δ1.55-1.65(m,6H),2.18(m,2H),2.23(m,2H),3.46(s,3H),3.74(s,3H),4.663d,J=7.2Hz,2H),5.47(t,J=7.2Hz,1H),6.45(s,1H),6.91(d,J=8.4Hz,2H),6.96(br.s,2H),7.06(br.s,1H),7.52(d,J=8.4Hz,2H)IR(KBr)3410,2924,2854,1609,1567,1523,1490,1462,1405,1254,1221,1198,1119,1069,824,813cm-1 |
I-182 | m.p.219-221℃1HNMR(DMSO-d6)δ2.22(t,J=5.4Hz,2H),2.32(t,J=5.4Hz,2H),3.30(s,3H),3.56(t,J=5.4Hz,2H),3.61(t,J=5.4Hz,2H),3.64(s,3H),4.59(d,J=6.6Hz,2H),5.54(t,J=6.6Hz,1H),6.39(s,1H),6.64(dd,J=8.4,2.1Hz,1H),6.73(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),6.89(d,J=8.4Hz,1H),7.43(d,J=8.4Hz,2H)IR(KBr)3392,2948,1609,1586,1522,1492,1271,1239,1219,1118,1076,1007,818cm-1 |
I-183 | m.p.149-150℃1HNMR(CDCl3)δ1.03(t,J=7.5Hz,3H),1.07(t,J=7.5Hz,3H),2.13(q,J=7.5Hz,2H),2.15(q,J=7.5Hz,2H),3.46(s,3H),3.75(s,3H),4.64(d,J=6.6Hz,2H),5.48(t,J=6.6Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.97(dd,J=7.8,1.5Hz,1H),6.97(d,J=7.8Hz,1H),7.06(d,J=1.5Hz,1H),7.52(d,J=8.7Hz,2H)IR(KBr)3398,2963,2934,1671,1610,1523,1493,1465,1407,1259,1224,1118,1071,813cm-1 |
I-184 | m.p.217-218℃1HNMR(CDCl3)δ3.86(s,3H),5.16(s,2H),5.72(s,1H),6.97-7.01(m,3H),7.12(dd,J=2.4,8.4Hz,1H),7.26(d,J=2.4Hz,1H),7.34-7.47(m,5H),7.54-7.58(m,2H),7.60(s,4H)IR(KBr)3600-3200(br),1605,1590,1493,1298,1282,1253,1206,1183,1022cm-1 |
I-185 | 1HNMR(CDCl3)δ1.21(t,J=6.9Hz,3H),1.77(s,3H),1.82(s,3H),2.38-2.46(m,2H),2.72-2.84(m,2H),3.18(s,3H),3.21(s,3H),3.35(s,3H),3.70(s,3H),4.06(q,J=6.9Hz,2H),4.63(d,J=6.6Hz,2H),5.52(t,J=6.6Hz,1H),6.75(s,1H),7.07(d,J=8.4Hz,1H),7.13(d.d,J=8.4&2.1Hz,1H),7.21(d,J=2.1Hz,1H),7.37(d,J=9.0Hz,2H),7.69(d,J=9.0Hz,2H)IR(KBr)1727,1517,1469,1364,1291,1234,1179,1152,1118,1080,1003cm-1 |
I-186 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.42-2.53(m,2H),2.72-2.86(m,2H),3.35(s,3H),3.69(s,3H),4.61(d,J=6.6Hz,2H),5.53(t,J=6.6Hz,1H),5.71(s,1H),6.68(d.d,J=8.4&2.1Hz,1H),6.76(s,1H),6.81(d,J=2.1Hz,1H),6.91(d,J=8.4Hz,2H),6.92(d,J=8.4Hz,1H),7.52(d,J=8.4Hz,2H)IR(KBr)3419,1707,1612,1518,1472,1390,1225,1078cm-1 |
I-187 | 1HNMR(CDC13)δ2.55(s,3H),3.54(s,3H),3.78(s,3H),5.18(s,1H),6.85(s,1H),6.91(d.d,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.04(d,J=2.1Hz,1H),7.33-7.48(m,5H),7.71(d,J=8.4Hz,2H),7.72(d,J=8.4Hz,2H)IR(KBr)3442,1617,1517,1485,1485,1394,1357,1331,1171,1124,1077,1067,1016cm-1 |
I-188 | 1HNMR(CDCl3)δ 2.68(s,3H),3.13(s,3H),3.54(s,3H),3.79(s,3H),5.19(s,2H),6.86(s,1H),7.16(d,J=8.7Hz,1H),7.31-7.50(m,7H),7.72(d,J=8.7Hz,2H),7.76(d,J=8.7Hz,2H)IR(KBr)1614,1513,1482,1366,1324,1177,1120,1079,1065,1016cm-1 |
I-189 | 1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.54(s,3H),3.79(s,3H),5.19(s,2H),6.86(s,1H),7.16(d,J=8.7Hz,1H),7.31-7.50(m,7H),7.72(d,J=8.7Hz,2H),7.76(d,J=8.7Hz,2H)IR(KBr)1614,1513,1482,1366,1324,1177,1120,1079,1065,1016cm-1 |
I-190 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.46(s,3H),3.76(s,3H),4.62(d,J=8.4Hz,2H),5.53(t,J=8.4Hz,1H),5.71(s,1H),5.85(s,1H),6.46(s,1H),6.94(d.d,J=8.1&1.8Hz,1H),6.98(d,J=8.1Hz,1H),7.05(d,J=1.8Hz,1H),7.71(d,J=8.1Hz,2H),7.77(d,J=8.1Hz,2H)IR(KBr)3552,3505,3466,1613,1509,1487,1397,1324,1288,1245,1163,1110,1065cm-1 |
I-191 | 1HNMR(CDCl3)δ3.02(s,6H),3.48(s,3H),3.76(s,3H),5.15(s,2H),5.67(s,1H),5.95(s,1H),6.47(s,1H),6.81(d,J=8.7Hz,2H),6.96(d.d,J=8.4&2.1Hz,1H),7.04(d,J=8.4Hz,1H),7.10(d,J=2.1Hz,1H),7.31-7.49(m,5H),7.55(d,J=8.7Hz,2H)IR(KBr)3543,3500,1605,1526,1486,1459,1245,1198,1110,1070,999cm-1 |
I-192 | mp122-124℃1HNMR(CDCl3)δ2.70(brs,3H),3.55-3.60(br,2H),3.60(s,3H),3.75(s,3H),3.81-3.83(m,2H),3.87(s,3H),5.15(s,2H),5.68(s,1H),6.69(s,1H),6.94(dd,J=2.1,8.4Hz,1H),6.97-7.03(m,3H),7.07(d,J=1.8Hz,1H),7.38-7.48(m,5H),7.51-7.56(m,2H)IR(KBr)3600-2800(br),1607,1597,1550,1518,1477,1462,1452,1392,1289,1248,1228,1175,1122,1096,1084,1015cm-1 |
I-193 | m.p.160-163℃1HNMR(CDCl3)δ3.60(s,3H),3.60-3.64(br,2H),3.76(s,3H),3.77-3.80(m,2H),5.15(s,2H),5.69(s,1H),5.88(s,1H),6.69(s,1H),6.90-6.94(m,3H),7.02(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.38-7.51(m,7H)IR(KBr)3600-3200(br),1613,1588,1519,1477,1462,1397,1256,1189,1117,1078,1011cm-1 |
I-194 | 1HNMR(CDCl3)δ3.02(s,6H),3.11(s,3H),3.50(s,3H),3.72(s,3H),4.43(brs,1H),4.58(brs,1H),5.18(s,2H),6.82(d,J=8.7Hz,2H),6.92(s,1H),7.16(d,J=9.3Hz,1H),7.31-7.51(m,7H),7.55(d,J=8.7Hz,2H)IR(KBr)3432,1611,1526,1476,1356,1291,1232,1186,1117,1079,1012cm-1 |
I-195 | m.p.157-158℃1HNMR(CDCl3)δ3.10(s,3H),3.21(s,3H),3.56(s,3H),3.69(s,3H),3.76(s,3H),4.47(s,2H),5.17(s,2H),6.68(s,1H),7.12(d,J=8.2Hz,1H),7.34-7.50(m,9H),7.63(d,J=8.6Hz,2H)IR(KBr):1748,1517,1476,1366,1232,1150,1114,968,873,812,791,750,707cm-1 |
I-196 | m.p.189-191℃(dec)1HNMR(DMSO-d6)δ3.45(s,3H),3.67(s,3H),4.25(s,2H),5.12(s,2H),6.66(dd,J=8.4,2.0Hz,1H),6.69(s,1H),6.77(d,J=2.0Hz,1H),6.80(d,J=8.6Hz,2H),6.98(d,J=8.4Hz,1H),7.33-7.54(m,7H),9.01(s,1H),9.54(brs,1H)IR(KBr):3422,3245,1733,1611,1596,1522,1478,1400,1262,1248,1222,1207,1130,1084,1011,836,781,744,699cm-1 |
I-197 | m.p.151-152℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.20(s,3H),3.21(s,3H),3.56(s,3H),3.70(s,3H),3.75(s,3H),4.47(s,2H),4.63(d,J=6.9Hz,2H),5.51(t,J=6.9Hz,1H),6.68(s,1H),7.05(d,J=8.4Hz,1H),7.36(dd,J=8.4,2.1Hz,1H),7.36(d,J=8.9Hz,2H),7.41(d,J=2.1Hz,1H),7.63(d,J=8.9Hz,2H)IR(KBr):1751,1517,1475,1366,1234,1150,1113,968,872,812,707cm-1 |
I-198 | m.p.155-156℃1HNMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),3.42(s,3H),3.67(s,3H),4.25(s,2H),4.54(d,J=6.8Hz,2H),5.49(t,J=6.8Hz,1H),6.65(dd,J=8.4,1.9Hz,1H),6.69(s,1H),6.73(d,J=1.9Hz,1H),6.84(d,J=8.4Hz,2H),7.36(d,J=8.4Hz,1H),7.41(d,J=8.4Hz,2H),8.85(s,1H),9.55(s,1H),11.2-13.6(brs,1H)IR(KBr):3411,3243,1733,1611,1594,1522,1477,1398,1247,1207,1126,1083,1015,835,788cm-1 |
I-199 | 1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.55(s,3H),3.80(s,3H),5.19(s,2H),6.88(s,1H),7.16(d,J=8.7Hz,1H),7.34(d,J=2.1Hz,1H),7.36-7.50(m,6H),7.81(d,J=8.4Hz,2H),7.98(d,J=8.4Hz,2H)IR(KBr)1698,1602,1481,1351,1232,1182,1079cm-1 |
I-200 | 1HNMR(CDCl3)δ2.42(s,3H),2.71(s,3H),3.03(s,3H),3.21(s,3H),3.56(s,3H),3.79(s,3H),5.17(s,2H),6.84(s,1H),7.19(d,J=8.4Hz,1H),7.22-7.30(m,3H),7.37(d,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.41-7.45(m,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1607,1519,1480,1177,1151,1079,970,875,798cm-1 |
I-201 | 1HNMR(CDCl3)δ2.38(s,3H),2.67(s,3H),3.14(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.15(s,2H),6.84(s,1H),7.14(d,J=8.4Hz,1H),7.17(brd,J=7.5Hz,1H),7.23-7.30(m,3H),7.34(dd,J=8.4,1.8Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=1.8Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1606,1519,1482,1180,1150,1078,1011,979,876,790cm-1 |
I-202 | 1HNMR(CDCl3)δ2.30(s,3H),2.38(s,6H),2.74(s,3H),2.94(s,3H),3.21(s,3H),3.57(s,3H),3.79(s,3H),5.13(s,2H),6.85(s,1H),6.91(brs,2H),7.37(d,J=8.7Hz,2H),7.40(brs,2H),7.41(dd,J=8.4,1.8Hz,1H),7.69(d,J=8.7Hz,2H)IR(CHCl3)1610,1518,1477,1370,1177,1149,1082,970,873cm-1 |
I-203 | 1HNMR(CDCl3)δ2.34(s,6H),2.66(s,3H),3.15(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.12(s,2H),6.84(s,1H),6.99(brs,1H),7.06(brs,2H),7.14(d,J=8.4Hz,1H),7.33(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1607,1519,1480,1178,1152,1097,1014,969,876,824,797cm-1 |
I-204 | 1HNMR(CDCl3)δ2.72(s,3H),3.16(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),3.94(s,3H),5.25(s,2H),6.84(s,1H),7.11(d,J=8.4Hz,1H),7.34(dd,J=8.4,2.1Hz,1H),7.38(d,J=8 7Hz.2H),7.42(d,J=2.1Hz,1H),7.55(d,J=8.4Hz,2H),7.68(d,J=8.7Hz,2H),8.09(d,J=8,4Hz,2H)IR(Nujol)1719,1610,1519,1480,1177,1151,1119,1080,1016,969,875,798cm-1 |
I-205 | m.p.153-157℃1HNMR(CDCl3)δ2.70(s,3H),3.16(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.13(s,2H),6.41(dd,J=3.3,2.0Hz,1H),6.49(d,J=3.3Hz,1H),6.84(s,1H),7.20(d,J=8.7Hz,1H),7.37(dd,J=8.7,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.46(d,J=2.0Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1605,1518,1482,1375,1361,1180,1150,1079,1013,977,876,814,800cm-1 |
I-206 | 1HNMR(CDCl3)δ2.41(s,3H),3.46(s,3H),3.75(s,3H),5.13(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.99(dd,J=8.4,2.1Hz,1H),7.07(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.22-7.34(m,3H),7.40(brd,J=7.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3471,3436,3339,1612,1581,1523,1489,1266,1245,1228,1185,1110,1070,1011,998,945,823,781cm-1 |
I-207 | 1HNMR(CDCl3)δ2.40(s,3H),3.45(s,3H),3.75(s,3H),5.11(s,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.95(dd,J=8.4,1.8Hz,1H),7.01(d,J=8.4Hz,1H),7.09(d,J=1.8Hz,1H),7.19(brd,J=7.5Hz,1H),7.22-7.34(m,3H),7.53(d,J=8.7Hz,2H)IR(Nujol)3410,1611,1589,1523,1489,1246,1225,1114,1071,1011,939,824,814,778cm-1 |
I-208 | m.p.230-236℃1HNMR(DMSO-d6)δ2.25(s,3H),2.35(s,6H),3.31(s,3H),3.65(s,3H),5.00(s,2H),6.39(s,1H),6.69(dd,J=8.4,1.8Hz,1H),6.76(d,J=1.8Hz,1H),6.84(d,J=8.7Hz,1H),6.90(brs,2H),7.06(d,J=8.4Hz,3H),7.44(d,J=8.7Hz,2H)IR(Nujol)3475,3361,1609,1579,1521,1260,1244,1110,1071,1012,988,822,782cm-1 |
I-209 | 1HNMR(CDCl3)δ2.35(s,6H),3.45(s,3H),3.75(s,3H),507(s,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.95(dd,J=8.4,1.8Hz,1H),7.01(brs,1H),7.02(d,J=8.4Hz,1H),7.06(brs,2H),7.08(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3410,1610,1588,1523,1489,1248,1225,1114,1071,1011,940,825,808,cm-1 |
I-210 | 1HNMR(CD3OD)δ3.37(s,3H),3.67(s,3H),5.25(s,2H),6.43(s,1H),6.77(dd ,J=8.4,2.1Hz,1H),6.84(d,J=8.7Hz,2H),6.89(d,J=2.1Hz,1H),6.94(d,J=8.4Hz,1H),7.45(d,J=8.7Hz,2H),7.60(d,J=8.4Hz,2H),8.04(d,J=8.4Hz,2H)IR(Nujol)3384,1694,1612,1591,1523,1488,1249,1113,1071,1013,940,826,812,765cm-1 |
I-211 | 1HNMR(CDCl3)δ3.45(s,3H),3.74(s,3H),5.09(s,3H),6.41(dd,J=3.3,1.8Hz,1H),6.45(s,1H),6.47(d,J=3.3Hz,1H),6.92(d,J=8.7Hz,2H),6.97(dd,J=8.4,2.1Hz,1H),7.07(d,J=2.1Hz,1H),7.08(d,J=8.4Hz,1H),7.48(dd,J=1.8,1.0Hz,1H),7.54(d,J=8.7Hz,2H)IR(Nujol)3410,1612,1589,1523,1489,1248,1226,1113,1071,1011,939,815,747cm-1 |
I-212 | m.p.156-158℃1HNMR(CDCl3)δ1.06(t,J=7.4Hz,3H),1.75(s,3H),2.10(q,J=7.4Hz,2H),3.46(s,3H),3.75(s,3H),4.64(d,J=7.0Hz,2H),5.52(t,J=7.0Hz,1H),6.45(s,1H),6.92(d,J=8.6Hz,2H),6.96(br.s,2H),7.06(br.s,1H),7.53(d,J=8.6Hz,2H)IR(KBr)3392,2960,2934,1610,1583,1568,1523,1492,1465,1406,1259,1241,1224,1198,1118,1071,824,812cm-1 |
I-213 | m.p.175-177℃1HNMR(CDCl3)δ1.77(s,3H),1.80(s,6H),34(s,3H),3.75(s,3H),4.59(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.96(br.s,2H),7.06(br.s,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3449,2929,1612,1581,1523,1489,1403,1262,1243,1228,1113,1070,823,807cm-1 |
I-214 | 1HNMR(CDCl3)δ1.66(tt,J=6.6,6.6Hz,2H),1.74(tt,J=6.6,6.6Hz,2H),2.32(t,J=6.6Hz,2H),2.34(t,J=6.6Hz,2H),2.71(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),4.62(d,J=6.9Hz,2H),5.60(m,1H),6.84(s,1H),7.09(d,J=8.7Hz,1H),7.34(dd,J=8.7,2.1Hz,1H),7.37(d,J=8.7Hz,2H),7.38(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)2941,1610,1518,1418,1365,1177,1151,1079,847,818cm-1 |
I-215 | 1HNMR(CDCl3)δ1.57-1.72(m,4H),2.05-2.13(m,4H),2.70(s,3H),3.21(s,3H),3.23(s,3H),3.56(s,3H),3.78(s,3H),4.48(s,2H),5.86(s,1H),6.84(s,1H),7.09(d,J=8.4Hz,1H),7.34(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.38(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(Br)2936,1610,1518,1481,1365,1177,1151,1079,818cm-1 |
I-216 | 1HNMR(CDCl3)δ1.74(d,J=6.6Hz,3H),2.54(d,J=2.1Hz,1H),2.70(s,3H),3.21(s,3H),3.24(s,3H),3.56(s,3H),3.78(s,3H),5.00(dd,J=6.6,2.1Hz,1H),6.84(s,1H),7.28(d,J=8.7Hz,1H),7.36(dd,J=8.7,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)3282,3023,2940,1609,1519,1481,1365,1177,1151,1079,970,815cm-1 |
I-217 | m.p.80-85℃1HNMR(CDCl3)δ1.62-1.77(m,4H),2.25-2.39(m,4H),3.46(s,3H),3.75(s,3H),4.60(d,J=7.0Hz,2H),5.63(m,1H),6.45(s,1H),6.92(d,J=8.6Hz,1H),6.95(br.s,2H),7.06(br.s,1H),7.68(d,J=8.6Hz,2H)IR(KBr)3282,3023,2940,1609,1519,1481,1365,1177,1151,1079,970,815cm-1 |
I-218 | 泡沫1HNMR(CDCl3)δ3.45(s,3H),3.77(s,3H),5.16(s,2H),5.69(brs,1H),5.86(s,1H),6.47(s,1H),6.95(dd,J=2.1,8.4Hz,1H),7.04(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.34-7.65(m,7H),7.83-7.92(m,2H)IR(CHCl3)3530,3022,1614,1588,1500,1485,1463,1405,1326,1290,1249,1168,1130,1117,1073,1011cm-1 |
I-219 | 泡沫1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.51-2.59(m,2H),2.74(s,3H),3.22(s,3H),3.55(s,3H),3.79(s,3H),4.07(t,J=6.6Hz,2H),5.21(m,1H),6.85(s,1H),7.08(d,J=8.7Hz,1H),7.35(dd,J=2.1,8.7Hz,1H),7.39(d,J=2.1Hz,1H),7.55-7.69(m,2H),7.81-7.87(m,2H)IR(CHCl3)3024,1609,1519,1481,1467,1396,1369,1321,1272,1179,1122,1082,1015cm-1 |
I-220 | m.p.124-126℃1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.50-2.57(m,2H),3.46(s,3H),3.76(s,3H),4.07(t,J=6.9Hz,2H),5.22(m,1H),5.69(brs,1H),5.84(s,1H),6.46(s,1H),6.93-7.05(m,3H),7.55-7.65(m,2H),7.82-7.91(m,2H).IR(KBr)3406,2935,1587,1519,1501,1488,1459,1359,1323,1304,1291,1274,1223,1170,1126,1113,1075,1018cm-1 |
I-221 | m.p.187-189℃1HNMR(CDCl3)δ2.33(s,3H),2.69(s,3H),3.21(s,3H),3.24(s,3H),3.55(s,3H),3.77(s,3H),4.17(s,2H),6.84(s,1H),7.12&7.25(ABq,J=8.7Hz,4H),7.31(dd,J=8.1Hz,J=1.5Hz,1H),7.38&7.67(ABq,J=8.7Hz,4H),7.42(d,J=8.1Hz,1H),7.46(d,J=1.5Hz,1H)IR(KBr)1512,1474,1417,1391,1356,1343,1177,1149,1082,1054,1013,976,961,939,867,854,844,820,812,799,523cm-1 |
I-222 | m.p.107-112℃1HNMR(CDCl3)δ2.73(s,3H),3.22(s,3H),3.28(s,3H),3.55(s,3H),3.77(s,3H),4.34(s,2H),6.84(s,1H),7.19(m,1H),7.30(dd,J=8.1Hz,J=1.8Hz,1H),7.34-7.41(m,3H),7.46(d,J=1.8Hz,1H),7.49(d,J=8.1Hz,1H),7.62-7.69(m,3H),8.55(m,1H)IR(KBr)1474,1389,1364,1179,1151,1081,937,873,813,797,523cm-1 |
I-223 | m.p.212-214℃1HNMR(CDCl3+CD3OD)δ3.45(s,3H),3.74(s,3H),4.13(s,2H),6.45(s,1H),6.90-6.96(m,3H),7.12(d,J=1.8Hz,1H),7.18-7.26(m,2H),7.48-7.54(m,3H),7.68(m,1H),8.63(m,1H)IR(KBr)3504,3272,1612,1596,1574,1521,1492,1463,1436,1405,1362,1310,1265,1222,1172,1116,1083,1052,1017,828cm-1 |
I-224 | m.p.199-200℃1HNMR(CDCl3)δ1.46(d,J=0.9Hz,3H),1.77(s,3H),3.44(s,3H),3.74(s,3H),3.90(m,2H),5.25(m,1H),6.04(brs,1H),6.45(s,1H),6.93&7.53(ABq,J=8.7Hz,4H),7.00(m,2H),7.05(m,1H)IR(KBr)3404,2999,2932,1612,1595,1522,1483,1454,1432,1401,1376,1357,1271,1223,1119,1080,1055,1015,974,938,829,817cm-1 |
I-225 | m.p.181-183℃1HNMR(CDCl3)δ1.37(s,9H),3.45(s,3H),3.75(s,3H),4.93(brs,1H),6.00(s,1H),6.46(s,1H),6.93&7.54(ABq,J=8.7Hz,4H),6.99(s,1H),7.01(dd,J=8.4Hz,J=1.5Hz,1H),7.16(d,J=1.5Hz,1H),7.49(d,J=8.4Hz,1H)IR(KBr)3495,3412,2959,2931,1610,1568,1552,1521,1499,1477,1459,1400,1364,1319,1270,1227,1192,1161,1116,1102,1090,1052,1019,942,833,817,588cm-1 |
I-226 | m.p.154-156℃1HNMR(CDCl3)δ2.33(s,3H),3.45(s,3H),3.75(s,3H),3.90(s,2H),4.68(s,1H),5.97(s,1H),6.45(s,1H),6.60(s,1H),6.90-6.98(m,3H),7.10(s,5H),7.41(d,J=8.1Hz,1H),7.53(m,2H)IR(KBr)3462,3368,1611,1550,1521,1499,1472,1455,1437,1401,1362,1321,1293,1267,1229,1187,1174,1164,1118,1077,1050,1011,821cm-1 |
I-227 | m.p.172-174℃1HNMR(CDCl3)δ1.38(d,J=1.2Hz,3H),1.76(s,3H),3.44(s,3H),3.75(s,3H),3.87(d,J=7.8Hz,2H),5.08(brs,1H),5.26(m,1H),6.08(s,1H),6.45(s,1H),6.94&7.53(ABq,J=8.7Hz,4H),7.11-7.14(m,2H),7.62(d,J=8.7Hz,1H),8.87(s,1H)IR(KBr)3412,1613,1520,1478,1458,1443,1404,1360,1346,1290,1270,1224,1200,1171,1119,1078,1054,945cm-1 |
I-228 | m.p.173-175℃1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.10(s,3H),2.50-2.61(m,2H),3.20(s,3H),3.21(s,3H),3.37(s,3H),3.71(s,3H),4.08(t,J=6.8Hz,2H),5.21-5.25(m,1H),6.73(s,1H),7.03-7.18(m,2H),7.23-7.25(m,2H),7.37(d,J=8.6Hz,2H),7.69(d,J=8.8Hz,2H)IR(KBr)3600-3200(br),3100-2800(br),1610,1527,1523,1477,1432,1365,1240,1172,1160,955,923cm-1 |
I-229 | m.p.148-150℃1HNMR(CDCl3)δ1.70(s,3H),1.77(s,3H),2.09(s,3H),2.48-2.62(m,2H),3.38(s,3H),3.73(s,3H),4.09(t,J=7.0Hz,2H),4.84(br,1H),5.19-5.22(m,1H),5.70(s,1H),6.71-6.96(m,5H),7.55(d,J=8.2Hz,2H)IR(KBr)3700-3200(br),3100-2800(br),1612,1584,1560,1448,1428,1390,1339,1315,1284,1246,1173,1160,1123,1018,999cm-1 |
I-230 | m.p.194-195℃1HNMR(CDCl3)δ2.10(s,3H),2.39(s,3H),3.10(s,3H),3.21(s,3H),3.36(s,3H),3.71(s,3H),5.13(s,2H),6.73(s,1H),7.14-7.18(m,8H),7.69(d,J=9.0Hz,2H)IR(KBr)3600-3200(br),3100-2800(br),1516,1475,1360,1332,1292,1266,1228,1199,1174,1151,1119,1098,1084,1005,968cm-1 |
I-231 | m.p.178-180℃1HNMR(CDCl3)δ2.09(s,3H),2.40(s,3H),3.37(s,3H),3.72(s,3H),497(brs,1H),5.10(s,2H),5.67(br,1H),6.70-6.75(m,2H),6.86-7.03(m,3H),7.22-7.26(m,2H),7.32-7.34(m,2H),7.54(d,J=8.2Hz,2H)IR(KBr)3600-3200(br),3100-2800(br),1611,1519,1479,1463,1388,1339,1314,1286,1258,1246,1225,1128,1098,1077,1007cm-1 |
I-232 | m.p.177-179℃1HNMR(CDCl3)δ2.54(s,3H),2.69(s,3H),3.13(s,3H),3.54(s,3H),3.77(s,3H),5.19(s,2H),6.85(s,1H),7.15(d,J=8.4Hz,2H),7.30-7.49(m,9H),7.53-7.59(m,2H)IR(CHCl3)1516,1476,1368,1266,1176,1118,1077,1080,1013,970,876,820cm-1 |
I-233 | 无定形粉末1HNMR(CDCl3)δ2.54(s,3H),3.46(s,3H),3.75(s,3H),5.15(s,2H),5.67(brs,1H),5.90(s,1H),6.46(s,1H),6.95(d.d,J=1.8&8.1Hz,1H),7.02(d,J=8.1Hz,1H),7.09(d,J=1.8Hz,1H),7.31-7.49(m,7H),7.55-7.62(m,2H)IR(CHCl3)3526,1517,1483,1414,1389,1289,1246,1192,1114.,1070,1010,937,818cm-1 |
I-234 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.73(s,3H),3.24(s,3H),3.53(s,3H),3.79(s,3H),3.96(s,3H),4.64(d,J=6.9Hz,2H),5.49(t,J=6.9Hz,1H),6.87(s,1H),7.09(d,J=8.4Hz,1H),7.35(d.d,J=8.4&2.1Hz,1H),7.39(d,J=2.1Hz,1H),7.71(d,J=8.4Hz,2H),8.13(d,J=8.4Hz,2H) |
I-235 | 1HNMR(CDCl3)δ2.69(s,3H),3.14(s,3H),3.55(s,3H),3.80(s,3H),5.20(s,2H),6.89(s,1H),7.16(d,J=9.0Hz,1H),7.34(d,J=2.1Hz,1H),7.36-7.51(m,6H),7.75(d,J=8.4Hz,2H),8.23(d,J=8.4Hz,2H)IR(KBr)3427,1724,1685,1606,1509,1481,1369,1272,1235,1179,1120,1084,1017cm-1 |
I-236 | 1HNMR(CDCl3)δ3.46(s,3H),3.77(s,3H),5.16(s,3H),6.50(s,3H),6.96(dd,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.34-7.50(m,5H),7.75(d,J=8.1Hz,2H),8.17(d,J=8.1Hz,2H) |
I-237 | 1HNMR(CDCl3)δ3.44(s,3H),3.76(s,3H),3.96(s,3H),5.16(s,2H),5.69(s,1H),5.89(s,1H),6.49(s,1H),6.96(d.d,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.32-1.50(m,5H),7.73(d,J=8.4Hz,2H),8.13(d,J=8.4Hz,2H)IR(KBr)3497,3443,1708,1608,1585,1487,1460,1443,1395,1281,1113,1068,1008cm-1 |
I-238 | 1HNMR(CDCl3)δ2.69(s,3H),3.13(s,3H),3.53(s,3H),3.79(s,3H),3.96(s,3H),5.19(s,2H),6.87(s,1H),7.15(d,J=9.0Hz,1H),7.31-7.50(m,7H),7.71(d,J=8.4Hz,2H),8.13(d,J=8.4Hz,2H)IR(KBr)1719,1608,1481,1366,1278,1118,1080,1017cm-1 |
I-239 | 1HNMR(CDCl3)δ2.38(s,3H),2.68(s,3H),3.12(s,3H),3.53(s,3H),3.79(s,3H),3.96(s,3H),5.14(s,2H),6.87(s,1H),7.15(d,J=8.7Hz,1H),7.21(d,J=8.4Hz,2H),7.34(d,J=8.4Hz,2H),7.36(d,J=8.7Hz,1H),7.40(d,J=2.1Hz,1H),7.71(d,J=8.7Hz,2H),8.13(d,J=8.4Hz,2H)IR(KBr)1718,1607,1519,1481,1355,1280,1232,1182,1121,1079,1018cm-1 |
I-240 | 1HNMR(CDCl3)δ2.70(s,3H),3.03(s,3H),3.12(s,3H),3.55(s,3H),3.77(s,3H),5.18(s,2H),6.78-6.89(broad,1H),6.86(s,1H),7.14(d,J=8.4Hz,1H),7.3 1-7.49(m,8H),7.55(d,J=8.4Hz,2H)IR(KBr)1604,1526,1483,1395,1374,1360,1292,1231,1177,1119,1078,1014cm-1 |
I-241 | 1HNMR(CDCl3)δ2.37(s,3H),2.69(s,3H),3.05(s,3H),3.12(s,3H),3.55(s,3H),3.77(s,3H),5.14(s,2H),6.85(s,1H),6.81-6.91(broad,2H),7.14(d,J=8.4Hz,1H),7.21(d,J=8.1Hz,1H),7.34(d,J=8.1Hz,2H),7.40(d,J=2.1Hz,1H),7.56(d,J=8.4Hz,2H)IR(KBr)1605,1529,1484,1396,1356,1275,1233,1178,1121,1078,1016cm-1 |
I-242 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.73(s,3H),3.03(s,6H),3.22(s,3H),3.55(s,3H),3.77(s,3H),4.63(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),6.75-6.91(broad,2H),6.86(s,1H),7.08(d,J=8.7Hz,1H),7.34(d.d,J=8.7&2.1Hz,1H),7.39(d,J=2.1Hz,1H),7.55(d,J=8,7Hz,1H)IR(KBr)1609,1529,1482,1363,1235,1178,1117,1078,1013cm-1 |
I-243 | IR(KBr)3409,1608,1509,1464,1367,1230,1175,1149,1079,1018cm-1 |
I-244 | 1HNMR(CDCl3)δ1.72(s,3H),1.76(s,3H),2.55(m,2H),3.22(s,3H),3.45(s,3H),3.72(s,3H),4.07(d,J=6.6Hz,2H),4.46(d,J=10.5Hz,1H),4.51(d,J=10.5Hz,1H),4.66(d,J=10.5Hz,1H),4.75(d,J=10.5Hz,1H),5.24(brs,1H),6.84(s,1H),6.95(d,J=8.7Hz,1H),7.02(s,1H),7.21(d,J=8.7Hz,1H),7.39(d,J=9.0Hz,2H)7.71(d,J=9.0Hz,2H)IR(KBr)3307,1609,1509,1465,1364,1235,1180,1152,1082,1021cm-1 |
I-245 | m.p.182-184℃1HNMR(CDCl3)δ2.42(s,3H),2.70(s,3H),3.13(s,3H),3.53(s,3H),3.77(s,3H),5.19(s,2H),6.86(s,1H),7.13-7.53(m,12H)IR(KBr)3434,3030,2937,1605,1522,1483,1366,1274,1235,1176,1119,1086,1011cm-1 |
I-246 | 1HNMR(CDCl3)δ2.58(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),3.91(s,3H),5.26(m,2H),684(s,1H),7.12(d,J=9.0Hz,1H),7.27-7.54(m,8H),7.60(d,J=8.7Hz,2H),7.90(d,J=2.1Hz,1H)IR(KBr)1728,1699,1605,1513,1480,1362,1239,1175,1150,1083,1017cm-1 |
I-247 | IR(KBr)1729,1607,1512,1479,1366,1234,1177,1151,1079,1015cm-1 |
I-248 | 1H NMR(CDCl3)δ1.75(s,3H),1.79 (s,3H),2.57(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),3.89(s,3H),4.63(d,J=6.6Hz,2H),5.49-5.58(m,1H),6.85(s,1H),6.93-7.00(m,3H),7.38(d,J=8.7Hz,2H),7.70(d,J=8.7Hz,2H)IR(KBr)1603,1518,1482,1365,1239,1176,1150,1078cm-1 |
I-249 | 泡沫1HNMR(CDCl3)δ2.30(br,1H),2.76-2.82(m,2H),3.64-3.68(m,2H)3.87(s,1H),5.14(s,2H),5.70(s,1H),6.70(dd,J=2.1,8.4Hz,1H),6.78(s,1H),6.84(d,J=1.8Hz,1H),6.97-7.01(m,3H),7.37-7.49(m,5H),7.56-7.61(m,2H)IR(KBr)3600-2800(br),1608,1583,1517,1464,1387,1287,1247,1225,1178,1082,1015cm-1 |
I-250 | m.p.104-105℃1HNMR(CDCl3)δ0.76(t,J=7.5Hz,3H),1.44-1.54(m,2H),3.61(s,3H),3.71(t,J=6.6Hz,2H),3.74(s,3H),3.87(s,3H),5.16(s,2H),5.63(s,1H),6.66(s,1H),6.90(dd,J=2.1,8.4Hz,1H),6.96-7.01(m,4H),7.04(d,J=1.8Hz,1H),7.37-7.48(m,5H),7.51-7.56(m,2H)IR(KBr)3600-2800(br),1608,1593,1518,1474,1462,1379,1294,1251,1226,1183,1109,1078,1040,1008cm-1 |
I-251 | m.p.103-105℃1HNMR(CDCl3)δ0.78(t,J=7.2Hz,3H),1.15-1.27(m,2H),1.43-1.51(m,2H),3.61(s,3H),3.73-3.77(m,2H),3.74(s,3H),3.87(s,3H),5.16(s,2H),5.63(s,1H),6.65(s,1H),6.90(dd,J=2.1,8.1Hz,1H),6.96-7.01(m,3H),7.04(d,J=2.1Hz,1H),7.37-7.48(m,5H),7.51-7.56(m,2H)IR(KBr)3600-2800(br),1607,1518,1467,1375,1288,1251,1179,1113,1084,1020,1008cm-1 |
1-252 | m.p.111.5-112.5℃1HNMR(CDCl3)δ0.78(t,J=7.5Hz,3H),1.15-1.27(m,2H),1.41-1.50(m,2H),3.10(s,3H),3.61(s,3H),3.73-3.78(m,2H),3.74(s,6H),5,18(s,2H),6.66(s,1H),6.96-7.01(m,2H),7.10(d,J=8.7Hz,1H),7.26-7.55(m,9H)IR(KBr)3600-2800(br),1609,1518,1464,1440,1375,1355,1289,1269,1249,1181,1170,1107,1080,1019cm-1 |
I-253 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),345(s,3H),3.76(s,3H),4.62(d,J=8.4Hz,2H),5.54(t,J=8.4Hz,1H),6.49(s,1H),6.91-6.99(m,2H),7.05(d,J=1.5Hz),7.74(d,J=8 7Hz,2H),8.15(d,J=8.7Hz,2H)IR(KBr)3474,1687,1607,1509,1417,1397,1316,1287,1240,1109,1071,1006cm-1 |
I-254 | 1HNMR(CDCl3)δ2.39(s,3H),3.45(s,3H),3.76(s,3H),5.11(s,2H),6.49(s,1H),6.94(dd,J=8.4&1.8Hz,1H),7.04(d,J=8.4Hz,1H),7.06(d,J=1.8Hz),7.19-7.38(m,4H),7.73(d,J=8.4Hz,2H),8.14(d,J=8.4Hz,2H)IR(KBr)3549,3466,1668,1603,1518,1489,1465,1449,1421,1397,1372,1288,1236,1186,1117,1074,1017cm-1 |
I-255 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.02(s,6H),3.48(s,3H),3.74(s,3H),4.61(d,J=7.2Hz,2H),5.53(t,J=7.2Hz,1H),5.66(s,1H),5.92(s,1H),6.47(s,1H),6.81(broad,2H),6.95(s,2H),7.06(s,1H),7.56(d,J=8.7Hz,2H)IR(KBr)3535,3494,3452,1606,1526,1487,1406,1357,1288,1242,1195,1112cm-1 |
I-256 | 1HNMR(CDCl3)δ2.39(s,3H),3.02(s,6H),3.48(s,3H),3.74(s,3H),5.10(s,2H),5.66(s,1H),5.93(s,1H),6.47(s,1H),6.82(d,J=8.4Hz,2H),6.96(dd,J=8.1&1.8Hz,1H),7.02(d,J=8.1Hz,1H),7.08(d,J=1.8Hz,1H),7.23(d,J=7.8Hz,2H),7.34(d,J=7.8Hz,2H),7.56(d,J=8.4Hz,2H)IR(KBr)3536,3379,1610,1586,1528,1489,1460,1443,1361,1288,1250,1225,1195,1117,1072,1008cm-1 |
I-257 | 1HNMR(CDCl3)δ1.71(s,3H),1.76(s,3H),2.49-2.60(m,2H),3.44(s,3H),3.70(s,3H),4.06(t,J=6.3Hz,2H),4.48(d,J=6.0Hz,2H),4.71(d,J=8.7Hz,2H),5.23(t,J=8.7Hz,1H),5.37(broads,1H),6.84(s,1H),6.91-6.97(m,1H),6.92(d,J=8.4Hz,2H),7.18-7.23(m,2H),7.52(d,J=8.7Hz,2H)IR(KBr)3398,1612,1518,1465,1389,1232,1174,1131,1101,1081,1023cm-1 |
I-258 | 1HNMR(CDCl3)δ:3.21(s,3H),3.41(s,3H),3.63(s,3H),3.77(s,3H),4.76(s,2H),6.15(s,2H),6.94(s,1H),6.99(d,J=8.7Hz,1H),7.23-7.49(m,9H),7.71(d,J=8.7Hz,2H)IR(KBr)3497,1738,1721,1607,1509,1469,1362,1242,1152,1056,1017cm-1 |
I-259 | 泡沫1HNMR(CDCl3)δ2.35(s,6H),2.73(s,3H),2.79(t,J=5.7Hz,2H),3.21(s,3H),3.31(s,3H),3.56(s,3H),3.78(s,3H),4.19(t,J=5.7Hz,2H),6.84(s,1H),7.09(d,J=8.4Hz,1H),7.34-7.41(m,4H),7.66-7.71(m,2H)IR(KBr)3600-2700(br),1519,1481,1365,1273,1200,1177,1151,1120,1079,1015cm-1 |
I-260 | 泡沫1HNMR(CDCl3+CD3OD)δ2.71(t,J=5.1Hz,2H),3.46(s,6H),3.73(s,6H),4.11(t,J=5.1Hz,2H),6.44(s,1H),6.87-6.99(m,4H),7.04(d,J=2.1Hz,1H),7.49-7.53(m,2H)IR(KBr)3600-2200(br),1607,1583,1519,1475,1407,1390,1275,1252,1226,1114,1062cm-1 |
I-261 | m.p.85-87℃1HNMR(CDCl3)δ3.49(s,3H),3.75(s,3H),5.15(s,2H),5.23(brs,1H),5.68(brs,1H),5.89(s,1H),6.43(s,1H),6.95(dd,J=8.3,2.1Hz,1H),7.03(d,J=8.3Hz,1H),7.08(d,J=2.1Hz,1H),7.08(t,J=8.7Hz,1H),7.33(ddd,J=8.7,2.1,1.2Hz1H),7.37-7.47(m,6H)IR(KBr)3410,1525,1488,1284,1248,1102,1010,759,704cm-1 |
I-262 | m.p.138-140℃1HNMR(CDCl3)δ1.77(s,3H),1.82,(s,3H),3.21(s,3H),3.22(s,3H),3.48(s,3H),3.78(s,3H),4.64(d,J=6.5Hz,2H),5.51(t,J=6.5Hz,1H),7.05(d,J=8.5Hz,1H),7.08(s,1H),7.14(dd,J=8.5,2.2Hz,1H),7.34(d,J=2.2Hz,1H),7.40(d,J=8.7Hz,2H),7.69(d,J=8.7Hz,2H),10.00(s,1H)IR(KBr)1693,1514,1470,1361,1348,1275,1239,1175,1151,979,969,867,845,815cm-1 |
I-263 | 泡沫1HNMR(DMSO-d6)δ1.74(s,3H),1.78(s,3H),3.32(s,3H),3.44(s,3H),3.76(s,3H),4.66(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),7.11(s,1H),7.23-7.25(m,3H),7.48(d,J=8.6Hz,2H),7.77(d,J=8.6Hz,2H),13.1(brs,1H)IR(KBr)3431,1737,1518,1471,1177,1151,972,864,849cm-1 |
I-264 | m.p.153.5-155.5℃1HNMR(CDCl3)δ2.58(s,3H),3.52(s,3H),3.77(s,3H),5.21(s,2H),5.83(s,1H),7.04-7.24(m,5H),7.30-7.49(m,5H),7.56-7.65(m,2H)IR(CHCl3)1607,1520,1481,1412,1368,1298,1267,1131,1080,1012,960,942,907,869,836,812cm-1 |
I-265 | dp>116℃1HNMR(CDCl3+CD3OD)δ2.69(s,3H),3.15(s,3H),3.16(s,3H),3.57(s,3H),3.80(s,3H),5.21(s,2H),6.88(s,1H),7.19(d,J=8.4Hz,1H),7.34-7.51(m,7H),7.83-7.90(m,2H),8.01-8.07(m,5H)IR(KBr)3434,3028,2934,1596,1519,1460,1365,1308,1276,1173,1148,1119,1108,1012,946,841,819cm-1 |
I-266 | m.p.136-138℃1HNMR(CDCl3)δ3.43(s,3H),3.75(s,3H),5.19(s,2H),5.98(s,1H),6.44(s,1H),7.04-7.52(m,10H),7.57-7.65(m,5H)IR(CHCl3)3496,1612,1521,1488,1454,1412,1391,1313,1267,1157,1113,1069,1010,934,825cm-1 |
I-267 | 泡沫1HNMR(CDCl3)δ2.38(s,3H),3.10)(s,3H),3.21(s,3H),3.41(s,3H),3.67(s,3H),3.77(s,3H),5.11(s,2H),6.93(s,1H),7.09(d,J=8.6Hz,1H),7.21(d,J=8.2Hz,2H),7.27(d,J=2.1Hz,1H),7.35(d,J=8.2Hz,2H),7.38(d,J=8.9Hz,2H),7.70(d,J=8.9Hz,2H)IR(KBr)1733,1518,1471,1367,1297,1177,1151,1118,1059,971,862,815cm-1 |
I-268 | 无定形1HNMR(DMSO-d6)δ1.64(s,3H),1.70(s,3H),2.44(q,J=7.2Hz,2H),3.30(s,3H),3.70(s,3H),3.93(t,J=7.2Hz,2H),5.26(t,J=7.2Hz,1H),6.64(dd,J=8.6,2.1Hz,1H),6.74(d,J=2.1Hz,1H),6.87(d,J=8.9Hz,2H),6.87(d,J=8.6Hz,1H),6.96(s,1H),7.48(d,J=8.9Hz,2H),8.84(s,1H),9.59(s,1H),12.8(brs,1H)IR(CHCl3)3594,3540,1743,1707,1520,1470,1260,1058cm-1 |
I-269 | m.p.206-208℃(dec.)1HNMR(DMSO-d6)δ2.32(s,3H),3.32(s,3H),3.66(s,3H),5.05(s,2H),6.66(dd,J=8.2,2.1Hz,1H),6.79(d,J=2.1Hz,1H),6.83(s,1H),6.84(d,J=8.6Hz,2H),6.89(d,J=8.2Hz,1H),7.20(d,J=8.0Hz,2H),7.38(d,J=8.0Hz,2H),7.45(d,J=8.6Hz,2H),8.91(s,1H),9.68(s,1H),12.7(brs,1H)IR(KBr)3413,1710,1612,1591,1520,1471,1377,1227,1083,1059,1013,837,809cm-1 |
I-270 | 泡沫1HNMR(CDCl3)δ2.42(s,3H),3.45(s,3H),3.75(s,3H),5.15(s,2H),5.68(s,1H),5.93(s,1H),6.47(s,1H),6.96(dd,J=1.8,8.1Hz,1H),7.03(d,J=1.8Hz,1H),7.25-7.28(m,2H),7.35-7.48(m,5H),7.52-7.56(m,2H)IR(CHCl3)3535,3014,1616,1588,1559,1523,1513,1490,1463,1455,1417,1396,1317,1290,1247,1194,1115,1072,1012cm-1 |
I-271 | m.p.143-145℃1HNMR(CDCl3)δ2.70(s,3H),3.12(s,3H),3.54(s,3H),3.73(s,3H),3.84(s,3H),5.18(s,2H),6.83(s,1H),7.00-7.07(m,2H),7.14(d,J=8.4Hz,1H),7.33-7.49(m,9H)IR(KBr)3434,2940,1609,1520,1482,1396,1369,1293,1283,1243,1178,1114,1080,1021,1009cm-1 |
I-272 | 泡沫1HNMR(CDCl3)δ3.45(s,3H),3.71(s,3H),3.86(s,3H),5.15(s,2H),5.67(s,1H),5.84(s,1H),6.42(s,1H),6.98(dd,J=1.8,8.4Hz,1H),7.01-7.07(m,2H),7.11(d,J=1.8Hz,1H),7.35-7.45(m,8H)IR(CHCl3)3534,3024,1617,1587,1517,1503,1483,1462,1409,1290,1247,1226,1215,1122,1104,1072,1013cm-1 |
I-273 | m.p.155-156℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.42(s,3H),2.73(s,3H),3.23(s,3H),3.53(s,3H),3.77(s,3H),4.63(d,J=6.6Hz,2H),5.49(m,1H),6.86(s,1H),7.09(d,J=8.4Hz,1H),7.25-7.53(m,6H)IR(KBr)3434,2935,1605,1522,1465,1388,1365,1292,1273,1176,1119,1084,1011cm-1 |
I-274 | m.p.138-140℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.73(s,3H),3.22(s,3H),3.54(s,3H),3.73(s,3H),3.84(s,3H),4.63(d,J=6.9Hz,2H),5.50(m,1H),6.83(s,1H),7.01-7.04(m,2H),7.08(d,J=8.4Hz,1H),7.26(d,J=0.6Hz,1H),7.34-7.43(m,3H)IR(KBr)3433,2937,1608,1519,1480,1400,1368,1292,1271,1244,1179,1112,1081,1011cm-1 |
I-275 | m.p.95-97℃1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.42(s,3H),3.45(s,3H),3.74(s,3H),4.61(d,J=6.6Hz,2H),5.52(m,1H),5.69(s,1H),6.47(s,1H),6.95-7.07(m,3H),7.25-7.28(m,2H),7.52-7.55(m,2H)IR(KBr)3479,2935,1613,1585,1523,1509,1490,1458,1415,1395,1362,1315,1249,1196,1112,1070,1005cm-1 |
I-276 | m.p.155-158℃1HNMR(CDCl3)δ1.76(d,J=0.9Hz,3H),1.82(d,J=0.9Hz,3H),3.45(s,3H),3.86(s,3H),4.61(d,J=6.9Hz,2H),5.35(m,1H),5.68(s,1H),5.82(s,1H),6.42(s,1H),6.96-7.09(m,4H),7.35-7.41(m,2H)IR(KBr)3428,3005,2952,1613,1583,1517,1505,1487,1464,1451,1411,1387,1359,1317,1289,1245,1140,1101,1070,1013cm-1 |
I-277 | m.p.173-175℃1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.42(s,3H),2.51-2.60(m,2H),2.75(s,3H),3.21(s,3H),3.53(s,3H),3.76(s,3H),4.07(t,J=6.9Hz,2H),5.21(m,1H),6.86(s,1H),7.06(d,J=8.7Hz,1H),7.25-7.28(m,2H),7.35(dd,J=2.1,8.7Hz,1H),7.40(d,J=2.1Hz,1H),7.50-7.53(m,2H)IR(KBr)3434,2934,1606,1523,1482,1388,1369,1277,1236,1177,1118,1085,1012cm-1 |
I-278 | m.p.151-154℃1HNMR(CDCl3)δ1.69(s,3H),1.74(d,J=0.9Hz,3H),2.51-2.59(m,2H),2.75(s,3H),3.21(s,3H),3.54(s,3H),3.73(s,3H),3.84(s,3H),4.07(t,J=6.9Hz,2H),5.21(m,1H),6.83(s,1H),7.00-7.08(m,3H),7.34-7.43(m,4H)IR(KBr)3434,2935,1610,1581,1522,1479,1399,1362,1283,1246,1180,1125,1114,1082,1046cm-1 |
I-279 | m.p.90-92℃1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.42(s,3H),2.49-2.56(m,2H),3.45(s,3H),3.74(s,3H),4.06(t,J=6.6Hz,2H),5.22(m,1H),5.67(s,1H),5.90(s,1H),6.46(s,1H),6.94-7.06(m,3H),7.25-7.28(m,2H),7.52-7.55(m,2H)IR(KBr)3529,3381,2927,1616,1586,1522,1490,1465,1418,1398,1360,1315,1289,1251,1225,1192,1114,1070,1011cm-1 |
I-280 | m.p.82-84℃1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.49-2.56(m,2H),3.45(s,3H),3.71(s,3H),3.85(s,3H),4.06(t,J=6.6Hz,2H),5.22(m,1H),5.67(s,1H),5.82(s,1H),6.42(s,1H),6.92-7.09(m,5H),7.35-7.43(m,2H)IR(KBr)3420,3326,2935,1615,1583,1518,1504,1486,1466,1410,1316,1289,1249,1122,1101,1071,1018cm-1 |
I-281 | m.p.166-168℃1HNMR(CDCl3)δ2.38(s,3H),2.69(s,3H),3.11(s,3H),3.54(s,3H),3.73(s,3H),3.84(s,3H),5.14(s,2H),6.83(s,1H),7.00-7.44(m,11H)IR(KBr)3434,2941,1608,1521,1498,1482,1466,1397,1368,1284,1243,1177,1113,1079,1019cm-1 |
I-282 | m.p.109-111℃1HNMR(CDCl3)δ2.39(s,3H),3.45(s,3H),3.71(s,3H),3.85(s,3H),5.10(s,2H),5.67(s,1H),5.83(s,1H),6.42(s,1H),6.95-7.41(m,11H)IR(CHCl3)3497,2935,1610,1583,1519,1499,1481,1465,1399,1312,1274,1245,1185,1120,1102,1067,1012cm-1 |
1-283 | 1HNMR(CDCl3)δ2.38(s,3H),2.68(s,3H),3.12(s,3H),3.53(s,1H),3.77(s,3H),5.14(s,2H),6.83(s,1H),7.10-7.24(m,5H),7.33(d,J=8.4Hz,1H),7.34(d,J=8.4Hz,2H),7.40(d,J=2.1Hz,1H)7.56-7.64(m,2H)IR(KBr)1603,1520,1482,1367,1297,1277,1251,1232,1176,1120,1084,1012cm-1 |
I-284 | 1HNMR(CDCl3)δ2.39(s,3H),3.45(s,3H),3.75(s,3H),5.10(s,2H),5.68(s,1H),5.88(s,1H),6.44(s,1H),6.95(dd,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.07(d,J=2.1Hz,1H),7.08-7.29(m,4H),7 34(d,J=8.4Hz,2H),7.56-7.65(m,2H)sIR(KBr)3504,3330,1604,1596,1490,1461,1455,1424,1360,1318,1242,1223,1121,1071,1009cm-1 |
I-285 | 1HNMR(CDCl3)δ2.69(s,3H),3.13(s,3H),3.56(s,3H),3.78(s,3H),5.19(s,2H),6.85(s,1H),7.05-7.15(m,1H),7.15(d,J=8.4Hz,1H),7.30-7.49(m,10H)IR(KBr)1610,1583,1517,1475,1455,1359,1296,1270,1239,1180,1116,1088,1013cm-1 |
I-286 | 1HNMR(CDCl3)δ3.47(s,3H),3.75(s,3H),5.15(s,2H),5.68(s,1H),5.89(s,1H),6.46(s,1H),6.95(dd,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.04-7.12(m,2H),7.35-7.51(m,9H)IR(KBr)3543,3346,1612,1586,1566,1518,1502,1479,1407,1362,1320,1239,1110,1068,1006cm-1 |
I-287 | 1HNMR(CDCl3)δ2.68(s,3H),3.14(s,3H),3.58(3,3H),3.81(s,3H),5.20(s,2H),6.88(s,1H),7.16(d,J=8.7Hz,1H),7.32-7.49(m,7H),7.60-7.68(m,1H),7.98-8.04(m,1H),8.24-8 29(m,1H),8.44-8.47(m,1H)IR(KBr)1609,1531,1362,1270,1239,1178,1122,1085,1014cm-1 |
I-288 | 1HNMR(CDCl3)δ3.49(s,3H),3.78(s,3H),5.17(s,2H),5.71(s,1H),5.83(s,1H),6.49(s,1H))6.95(dd,J=12.3&1.2Hz,1H),7.02(d,J=12.3Hz,1H),7.08(d,J=1.2Hz,1H),7.33-7.50(m,5H),7.60-7.68(m,1H),7.97-8.06(m,1H),8.21-8.27(m,1H),8.52(s,1H)IR(KBr)3528,3358,1588,1527,1499,1454,1406,1348,1314,1241,1122,1070,1009cm-1 |
I-289 | 1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.55(s,3H),3.77(s,3H),5.19(s,2H),6.79-6.88(m,1H),6.86(s,1H),7.02-7.10(m,2H),7.15(d,J=8.4Hz,1H),7.26-1.50(m,8H)IR(KBr)3479,3388,1623,1603,1518,1478,1396,1358,1176,1118,1081,1013cm-1 |
I-290 | 1HNMR(CDCl3)δ3.11(s,3H),3.45(s,3H),3.77(s,3H),5.17(s,2H),6.05(s,1H),6.46(s,1H))7.00-7.18(m,1H),7.14(d,J=8.4Hz,1H),7.33-7.50(m,9H),7.52(d,J=2.1Hz,1H)IR(KBr)3504,1612,1578,1519,1498,1464,1391,1355,1290,1276,1239,1183,1167,1107,1070,1004cm-1 |
I-291 | 1HNMR(CDCl3+CD3OD)δ3.44(s,3H),3.75(s,3H),4.74(s,2H),5.13(s,2H),1H),6.86-6.95(m,3H),6.99(d,J=8.7Hz,1H),7.30-7.48(m,7H),7.52(d,J=8.7Hz,2H)IR(KBr)3433,1707,1611,1518,1473,1463,1379,1250,1174,1132,1089,1058,1016cm-1 |
I-292 | 1HNMR(CDCl3+CD3OD)δ3.41(s,3H),3.62(s,3H),3.75(s,3H),4.74(s,2H),5.15(s,2H),6.87-7.01(m,4H),7.30-7.55(m,9H)IR(KBr)3386,1722,1611,1518,1464,1343,1271,1245,1233,1215,1168,1082,1060,1021cm-1 |
I-293 | 1HNMR(CDCl3)δ2.38(s,3H),2.69(s,3H),3.12(s,3H),3.56(s,3H),3.78(s,3H),5.14(s,2H),6.85(s,1H),7.05-7.45(m,12H)IR(KBr)1607,1584,1519,1479,1401,1364,1348,1280,1237,1178,1164,1115,1081,1016cm-1 |
I-294 | 泡沫1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.36(d,J=2.1Hz,1H),4.55(s,2H),4.76(d,J=2.1Hz,1H),6.45,(s,1H),6.92(d,J=8.7Hz,2H),6.99(d,J=8.4Hz,1H),7.20(dd,J=1.5and8.4Hz,1H),7.11(d,J=1.5Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3425,1612,1588,1523,1487,1295,1268,1228,1113,1069,825cm-1 |
I-295 | 泡沫1HNMR(CDCl3)δ2.78(s,3H),3.21(s,3H),3.23(s,3H),3.55(s,3H),3.78(s,3H),4.79(d,J=6.6Hz,2H),6.21(t,J=6.6Hz,1H),6.85(s,1H),7.08(d,J=8.7Hz,1H),7.37(dd,J=8.7,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1632,1607,1519,1482,1180,1150,1079,1011,976,876,814,798cm-1 |
I-296 | 泡沫1HNMR(CD3OD)δ3.38(s,3H),3.68(s,3H),4.12(brs,2H),4.65(brs,2H),5.01(m,2H),6.43(s,1H),6.78(dd,J=8.7,1.8Hz,1H),6.85(d,J=8.7,2H),6.86(d,J=1.8Hz,1H),6.94(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3411,1612,1591,1520,1485,1461,1253,1223,1115,1008,971,944,842,810,785cm-1 |
I-297 | 泡沫1HNMR(CD3OD)δ3.38(s,3H),3.68(s,3H),4.73(d,J=5.1Hz,2H),4.23(d,J=5.1Hz,2H),5.83(m,2H),6.43(s,1H),6.79(dd,J=8.7,1.8Hz,1H),6.85(d,J=8.7,2H),6.86(d,J=1.8Hz,1H),6.94(d,J=8.7Hz,2H)IR(Nujol)3393,1611,1588,1523,1489,1460,1248,1114,1071,1013,940,824cm-1 |
I-298 | 泡沫1HNMR(CD8OD)δ1.77(s,3H),3.38(s,3H),3.68(s,3H),4.00(s,2H),5.72(d,J=6.3Hz,2H),5.81(t,J=6.3Hz,1H),6.43(s,1H),6.79(dd,J=8.7,1.8Hz,1H),6.85(d,J=8.7,2H),6.85(d,J=1.8Hz,1H),6.94(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3384,1608,1585,1523,1494,1457,1262,1242,1227,1116,1078,1008,985,822,781cm-1 |
I-299 | 泡沫1HNMR(CD3OD)δ1.87(s,3H),3.83(s,3H),3.68(s,3H),4.17(s,2H),4.69(d,J=6.6Hz,2H),5.68(t,J=6.3Hz,1H),6.43(s,1H),6.79(dd,J=8.7,1.8Hz,1H),6.85(d,J=8.4,2H),6.85(d,J=1.8Hz,1H),6.94(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3350,3236,1606,1589,1524,1490,1463,1247,1227,1079,1011,992,819,790cm-1 |
I-300 | 泡沫1HNMR(CDCl3)δ1.87(s,3H),2.10(s,3H),3.45(s,3H),3.74(s,3H),4.68(s,2H),4.71(d,J=6.0Hz,2H),5.77(t,J=6.0Hz,1H),6.44(s,1H),6.92(d,J=8.0Hz,2H),6.95(m,2H),7.07(brs,1H),7.53(d,J=6.0Hz,2H)IR(Nujol)3409,1724,1612,1587,1523,1489,1466,1239,1114,1071,1012,940,825,781cm-1 |
I-301 | 泡沫1HNMR(CD3OD)δ2.93(d,J=2.1Hz,1H),3.38(s,3H),3.68(s,3H),4.06(dd,J=9.9,7.8Hz,1H),4.20(dd,J=9.9,3.6Hz,1H),4.74(ddd,J=7.8,3.6,2.1Hz,1H),6.44(s,1H),6.80(dd,J=8.4,1.8Hz,1H),6.85(d,J=8.7,2H),6.87(d,J=1.8Hz,H1),6.96(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3282,1655,1612,1588,1523,1489,1460,1254,1226,1072,1013,940,825cm-1 |
I-302 | 泡沫1HNMR(CD3OD)δ3.30(s,3H),3.68(s,3H),4.75(d,J=5.1Hz,2H),6.44(s,1H),6.80(dd,J=8.4,1.8Hz,1H),6.85(d,J=8.4,2H),6.92(d,J=1.8Hz,1H),6.99(d,J=8.7Hz,1H),7.42(t,J=5.1Hz,1H),7.46(d,J=8.4Hz,2H)IR(Nujol)3474,3316,1678,1611,1584,1523,1487,1458,1268,1231,1115,1171,1011,942,824,758cm-1 |
I-303 | 泡沫1HNMR(CD3OD)δ1.24(d,J=7.2Hz,3H),3.38(s,3H),3.68(s,3H),4.12(q,J=7.2Hz,2H),4.75(d,J=4.8Hz,2H),6.43(s,1H),6.80(dd,J=8.4,1.8Hz,1H),6.85(d,J=8.7,2H),6.91(d,J=1.8Hz,1H),6.99(d,J=8.4Hz,2H),7.46(d,J=8.7Hz,2H),7.52(t,J=4.8Hz,1H)IR(Nujol)3306,1715,1612,1587,1523,1487,1460,1266,1232,1115,1070,824,760cm-1 |
I-304 | 泡沫1HNMR(CDCl3)δ2.34(s,3H),2.38(s,3H),2.70(s,3H),3.07(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.13(s,2H),6.84(s,1H),7.03(d,J=7.8Hz,1H),7.06(s,1H),7.18(d,J=8.4Hz,1H),7.28(d,J=7.8Hz,1H),7 36(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)1611,1518,1480,1365,1177,1151,1080,876,816cm-1 |
I-305 | 泡沫1HNMR(CDCl3)δ1.25(d,J=6.9Hz,6H),2.67(s,3H),2.93(q,J=6.9Hz,1H)3.13(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.15(s,2H),6.84(s,1H),7.16(d,J=8.7Hz,1H),7.26(d,J=8.4Hz,2H),7.34(dd,J=2.4,8.7Hz,1H),7.38(d,J=8.4Hz,4H),7.40(d,J=2.4Hz,1H),7.68(d,J=8.4Hz,2H)IR(KBr)1609,1519,1481,1365,1177,1151,1080,875,819cm-1 |
I-306 | 泡沫1HNMR(CDCl3)δ2.62(s,3H),3.15(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),5.36(s,2H),6.84(s,1H),7.18(d,J=8.7Hz,1H),7.26(s,1H),7.33(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.51(m,2H),7.57(dd,J=1.8,8.4Hz,1H),7.68(d,J=8.7Hz,2H),7.84-7.93(m,4H)IR(KBr)1608,1519,1480,1364,1177,1151,1079,876,819,797cm-1 |
I-307 | 泡沫1HNMR(CDCl3)δ2.64(s,3H),3.21(s,3H),3.28(s,3H),3.55(s,3H),3.77(s,3H),5.51(s,2H),6.83(s,1H),7.18(d,J=8.4Hz,1H),7.31(dd,J=2.4,8.4Hz,1H),7.37(d,J=8.7Hz,2H),7.42(d,J=2.4Hz,1H),7.58(dt,J=2.4,7.2Hz,1H),7.67(d,J=8.7Hz,2H),7.74(d,J=8.4Hz,1H),7.76(dt,J=2.4,7.2Hz,1H),7.85(d,J=7.2Hz,1H),8.06(d,J=7.2Hz,1H),8.23(d,J=7.2Hz,1H)IR(KBr)1603,1519,1480,1365,1177,1151,1080,876,824,797cm-1 |
I-308 | 泡沫1HNMR(CDCl3)δ2.76(s,3H),3.17(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.25(s,2H),6.85(s,1H),7.12(d,J=8.7Hz,1H),7.35(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.42(d,J=2.1Hz,1H),7.61(d,J=8.7Hz,2H),7.67(d,J=8.4Hz,2H),7.68(d,J=8.7Hz,2H)IR(KBr)1610,1522,1489,1402,1245,1181,1164,1110,1071,821,805cm-1 |
I-309 | m.p.221-222℃1HNMR(CDCl3)δ2.36(s,3H),2.38(s,3H),3.46(s,3H),3.75(s,3H),5.09(s,2H),6.45(s,1H),6.92(d,J=8.4Hz,2H),6.98(dd,J=2.1,8.1Hz,1H),7.06(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.08(s,1H),7.28(d,J=8.4Hz,1H),7.53(d,J=8.4Hz,2H)IR(KBr)3475,1610,1522,1489,1402,1245,1181,1164,1110,1071,821,805cm-1 |
I-310 | m.p.153-155℃1HNMR(CDCl3)δ1.27(d,J=6.9Hz,6H),2.95(q,J=6.9Hz,1H),3.45(s,3H),3.74(s,3H),5.11(s,2H),6.45(s,1H),6.91(d,J=8.4Hz,2H),6.96(dd,J=2.1,8.1Hz,1H),7.03(d,J=8.1Hz,1H),708(d,J=2.1Hz,1H),7.28(d,J=8.1Hz,2H),7.38(d,J=8.1Hz,2H),7.53(d,J=8.4Hz,2H)IR(KBr)3486,1611,1522,1489,1265,1113,1072,1011,823cm-1 |
I-311 | m.p.176-177℃1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.32(s,2H),6.45(s,1H),6.91(d,J=8.4Hz,2H),6.97(dd,J=2.1,8.4Hz,1H),7.06(d,J=8.4Hz,1H),7.10(d,=2.1Hz,1H),7.53(d,J=8.4Hz,2H),7.50-7.57(m,3H),7.82-7.92(m,4H)IR(KBr)3476,1610,1522,1488,1469,1401,1263,1246,1173,1112,1073,1014,1002,819,806cm-1 |
I-312 | m.p.235-237℃1HNMR(CDCl3)δ3.44(s,3H),3.73(s,3H),5.49(s,2H),6.44(s,1H),692(d,J=8.4Hz,2H),6.93(dd,J=2.1,8.4Hz,1H),7.14(d,J=2.1Hz,1H),7.18(d,J=8.4Hz,1H),7.38(d,J=8.4Hz,1H),7.52(d,J=8.4Hz,2H),7.58(dd,J=7.2,7.2Hz,1H),7.77(dd,J=7.2,7.2Hz,1H),7.85(d,J=7.2Hz,1H),8.21(d,J=7.2Hz,1H),8.22(d,J=7.2Hz,1H)IR(KBr)3378,1609,1522,1488,1268,1229,1205,1114,1072,1016,825,782cm-1 |
I-313 | m.p.159-161℃1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.22(s,2H),6.45(s,1H),6.92(d,J=8.4Hz,2H),6.96(br.s,2H),7.11(br.s,1H),7.53(d,J=8.4Hz,2H),7.57(d,J=8.4Hz,2H),7.68(d,J=8.4Hz,2H),IR(KBr)3433,1613,1523,1490,1326,1251,1166,1113,1066,1014,825,cm-1 |
I-314 | m.p.92-93℃1HNMR(CDCl3)δ1.63(s,3H),1.74(s,3H),2.34-2.39(m,1H),2.67-2.72(m,2H),3.47(s,3H),3.74(s,3H),4.52-4.54(m,2H),5.30-5.33(m,2H),6.78-6.97(m,4H),7.20(d,J=7.2Hz,1H),7.56(d,J=8.0Hz,2H)IR(KBr)3410,2932,1613,1519,1473,1444,1390,1263,1228,1174cm-1 |
I-315 | m.p.85-86℃1HNMR(CDCl3)δ1.76(s,3H),1.83(s,3H),2.17-2.40(m,1H),2.65-2.71(m,2H),3.24(s,3H),3.46(s,3H),3.80(s,3H),4.50-4.52(m,2H),6.70(s,1H),7.28-7.43(m,5H),7.73(d,J=8.6Hz,2H)IR(KBr)3432,2938,1731,1513,1469,1366,1180,1151,970,868cm-1 |
I-316 | m.p.179-180℃1HNMR(CDCl3)δ1.72(s,3H),1.76(s,3H),2.15-2.35(m,1H),2.61-2.70(m,2H),3.46(s,3H),3.76(s,3H),4.47-4.50(m,2H),6.68(s,1H),7.17-7.52(m,5H),7.69(d,J=8.4Hz,2H)IR(KBr)3427,2934,1612,1576,1519,1465,1443,1415,1376,1228,1174,846cm-1 |
I-317 | m.p.141-142℃1HNMR(CDCl3)δ1.75(s,3H),1.80(s,3H),3.21(s,3H),3.39(s,3H),3.68(s,3H),3.77(s,3H),4.61(d,J=7.2Hz,2H),5.50(t,J=7.0Hz,1H),6.93(s,1H),6.99-7.33(m,5H),7.57-7.65(m,2H)IR(KBr)3432,2938,1724,1519,1474,1365,1346,1294,1262,1244,1220,1163,1119,1059,953,842,805cm-1 |
I-318 | m.p.127-128℃1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.54(dt,J=4.2,4.6Hz,2H),3.20(s,3H),3.39(s,3H),3.68(s,3H),3.76(s,3H),4.05(t,J=4.4Hz,2H),5.21(t,J=4.6Hz,1H),6.93(s,1H),7.00(d,J=5.6Hz,1H),7.11-7.18(m,2H),7.25-7.35(m,3H),7.61(dd,J=3.8,5.8Hz)IR(KBr)3447,2974,2940,1740,1519,1471,1365,1343,1295,1262,1226,1182,1161,1119,1058,952,843,814cm-1 |
I-319 | m.p.171-172℃1HNMR(CDCl3)δ2.38(s,3H),3.10(s,3H),3.39(s,3H),3.66(s,3H),3.77(s,3H),5.11(s,2H),6.93(s,1H),7.07-7.36(m,9H),7.61(dd,J=3.4,5.6Hz,2H)IR(KBr)3431,2937,1724,1519,1474,1440,1346,1296,1259,1243,1222,1165,1121,1060,953,843,804cm-1 |
I-320 | m.p.155-156℃1HNMR(CDCl3)δ3.40(s,3H),3.69(s,3H),3.77(s,3H),5.13(s,2H),5.70(brs,1H),6.82-7.42(m,5H),7.39-7.42(m,5H),7.62(dd,J=5.4,8.6Hz)IR(KBr)3550,3481,2956,1723,1519,1467,1435,1344,1285,1261,1238,1223,1130,1058,1013,840cm-1 |
I-321 | m.p.159-160℃1HNMR(CDCl3)δ3.11(s,3H),3.40(s,3H),3.66(s,3H),3.77(s,3H),5.16(s,2H),6.93(s,1H),7.07-7.49(m,5H),7.62(dd,J=3.0,8.4Hz,2H)IR(KBr)3441,2952,1732,1519,1469,1445,1381,1356,1342,1291,1273,12443,1226,1162,1119,1081,1057,999,950,842,805cm-11 |
I-322 | m.p.160-161℃1HNMR(CDCl3)δ2.37(s,3H),2.93(s,3H),3.19(s,3H),3.22(s,3H),3.55(s,3H),3.79(s,3H),5.23(s,2H),6.86(s,1H),7.20(d,J=8.1Hz,2H),7.30(d,J=8.1Hz,2H),7.36-7.41(m,2H),7.64-7.70(m,2H),7.74(d,J=2.1Hz,1H),7.83(d,J=2.1Hz,1H),10.16(s,1H)IR(CHCl3)3027,2940,1692,1473,1373,1227,1152,1085cm-1 |
I-323 | 粉末1HNMR(CDCl3)δ2.37(s,3H),2.86(s,3H),3.13(s,3H),3.21(s,3H),3.54(s,3H),3.79(s,3H),4.64(s,2H),5.11(s,2H),6.85(s,1H),7.21(d,J=7.8Hz,2H),7.32-7.44(m,6H),7.65-7.70(m,2H)IR(CHCl3)3026,2939,1475,1372,1228,1178,1151,1084cm-1 |
I-324 | 粉末1HNMR(CDCl3)δ1.89-1.98(brs,1H),2.39(s,3H),3.45(s,3H),3.75(s,3H),4.77(s,2H),5.01(s,3H),5.46(s,1H),5.99(s,1H),6.45(s,1H),6.45-6.95(m,2H),7.05(s,2H),7.24(d,J=8.1Hz,2H),7.38(d,J=8.1Hz,2H),7.50-7.56(m,2H)IR(CHCl3)3514,2937,1731,1613,1522,1484,1403,1228,1173,1082cm-1 |
I-325 | 粉末1HNMR(CDCl3)δ2.31(s,3H),2.88(s,3H),3.07(s,3H),3.22(s,3H),3.51(s,3H),3.74(s,3H),5.23(s,2H),6.83(s,1H),7.11-7.18(m,2H),7.32-7.41(m,4H),7.62-7.68(m,3H),8.03(s,1H)IR(CHCl3)3026,2939,1742,1472,1374,1227,1179,1129,1085cm-1 |
I-326 | 粉末1HNMR(CD3OD)δ2.33(s,3H),3.38(s,3H),3.68(s,3H),5.11(s,2H),6.44(s,1H),6.82-6.88(m,2H),6.99(d,J=1.8Hz,1H),7.13-7.19(m,3H),7.42-7.50(m,4H)IR(KBr)3411,2935,1680,1611,1520,1457,1404,1281,1230,1114cm-1 |
I-327 | 粉末1HNMR(CDCl3)δ1.72(s,3H),1.79(s,3H),3.12(s,3H),3.21(s,3H),3.27(s,3H),3.52(s,3H),3.53(s,3H),4.81(d,J=7.5Hz,2H),5.51(m,1H),7.38-7.43(m,2H),7.45-7.50(m,2H),7.80(d,J=2.1Hz,1H),7.97(d,J=2.1Hz,1H)IR(CHCl3)3032,2941,1543,1377,1209cm-1 |
I-328 | m.p.205-206℃1HNMR(CDCl3)δ1.75(s,3H),1.80(s,3H),3.41(s,3H),3.47(s,3H),4.66(d,J=6.6Hz,2H),5.06(s,1H),5.53(m,1H),6.33(s,1H),6.89-6.95(m,2H),7.28-7.34(m,2H),7.38-7.40(m,1H),7.99(d,J=2.1Hz,1H),10.83(d,J=0.6Hz,1H)IR(KBr)3476,2940,1614,1532,1371,1238,1094,1035cm-1 |
I-329 | m.p.144-145℃1HNMR(CDCl3)δ2.83(s,3H)3.22(s,3H),3.28(s,3H),3.55(s,3H),3.79(s,3H),6.86(s,1H),7.37-7.45(m,3H),7.47-7.53(m,3H),7.65-7.70(m,2H)IR(KBr)3434,3019,2939,1515,1480,1370,1176,1150,1081cm-1 |
I-330 | 无定形1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.54(q,J=7.2Hz,2H),3.21(s,3H),3.41(s,3H),3.65(s,3H),3.77(s,3H),4.03(t,J=7.2Hz,2H),5.23(t,J=7.2Hz,1H),6.94(s,1H),6.98(t,J=8.6Hz,1H),7.05(ddd,J=8.6,2.1,0.9Hz,1H),7.14(dd,J=12.0,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.71(d,J=8.7Hz,2H)IR(CHCl3)1732,1521,1471,1375,1262,1230,1150,1061,874cm-1 |
I-331 | m.p.146-148℃1HNMR(CDCL3)δ1.56(s,3H),1.80(s,3H),3.21(s,3H),3.41(s,3H),3.65(s,3H),3.77(s,3H),4.61(d,J=6.9Hz,2H),5.54(t,J=6.9Hz,1H),6.94(s,1H),6.98(t,J=8.4Hz,1H),7.05(ddd,J=8.4,2.4,0.9Hz,1H),7.14(dd,J=12.0,2.4Hz,1H),7.38(d,J=8.7Hz,2H),7.71(d,J=8.7Hz,2H)IR(KBr)1736,1519,1471,1357,1257,1150,1061,984,872cm-1 |
I-332 | m.p.170-171℃1HNMR(DMSO-d6)δ1.73(s,3H),1.77(s,3H),3.31(s,3H),3.73(s,3H),4.62(d,J=7.0Hz,2H),5.48(t,J=7.0Hz,1H),6.87(d,J=8.9Hz,2H),7.00(s,1H),7.03(ddd,J=8.7,2.3,0.9Hz,1H),7.10(dd,J=12.3,2.3Hz,1H),7.18(t,J=8.7Hz,1H),7.48(d,J=8.9Hz,2H),9.60(s,1H),12.9(brs,1H)IR(KBr)3258,1687,1615,1523,1465,1373,1260,1233,1057,994,835,823cm-1 |
I-333 | m.p.172-174℃1HNMR(CDCl3)δ3.21(s,3H),3.41(s,3H),3.61(s,3H),3.77(s,3H),5,17(s,2H),6.94(s,1H),7.01-7.04(m,2H),7.13-7.18(m,1H),7.33-7.49(m,7H),7.70(d,J=9.0Hz,2H)IR(KBr)1725,1522,1463,1346,1261,1230,1147,1058,878,756cm-1 |
I-334 | m.p.149-151℃1HNMR(CDCl3)δ2.36(s,3H),3.21(s,3H),3.41(s,3H),3.61(s,3H),3.77(s,3H),5.13(s,2H),6.93(s,1H),7.00-7.03(m,2H),7.12-7.17(m,1H),7.20(d,J=8.4Hz,2H),7.35(d,J=8.4Hz,2H),7.38(d,J=8.7Hz,2H),7.70(d,J=8.7Hz,2H)IR(KBr)1731,1519,1472,1370,1298,1152,1058,874,791cm-1 |
I-335 | m.p.173-174℃1HNMR(DMSO-d6)δ1.64(s,3H),1.70(s,3H),2.45(q,J=6.9Hz,2H),3.31(s,3H),3.73(s,3H),4.04(t,J=6.9Hz,2H),5.22(t,J=6.9Hz,1H),6.87(d,J=8.7Hz,2H),6.99(s,1H),7.03(ddd,J=8.7,2.1,0.9Hz,1H),7.10(dd,J=12.3,2.1Hz,1H),7.16(t,J=8.7Hz,1H),7.48(d,J=8.7Hz,2H),9.61(s,1H),12.9(brs,1H)IR(KBr)3303,1696,1523,1473,1371,1261,1241,1061,1009,839cm-1 |
I-336 | m.p.222-224℃1HNMR(DMSO-d6)δ3.31(s,3H),3.73(s,3H),5.26(s,2H),6.87(d,J=8.7Hz,2H),7.00(s,1H ),7.03-7.07(m,1H),7.13(dd,J=12.3,2.1Hz,1H),7.26(t,J=8.7Hz,1H),7.36-7.52(m,7H),9.61(s,1H),12.9(brs,1H)IR(KBr)3268,1689,1523,1465,1374,1261,1055,836cm-1 |
I-337 | m.p.205-206℃1HNMR(DMSO-d6)δ2.32(s,3H),3.31(s,3H),3.72(s,3H),5.15(s,2H),6.87(d,J=8.7Hz,2H),6.99(s,1H),7.04(ddd,J=9.0,1.9,0.9Hz,1H),7.12(dd,J=12.3,1.9Hz,1H),7.23(d,J=8.0Hz,2H),7.24(t,J=9.0Hz,1H),7.38(d,J=8.0Hz,2H),7.48(d,J=8.7Hz,2H),9.60(s,1H),12.9(brs,1H)IR(KBr)3303,1696,1523,1464,1261,1241,1056,993,838,811,791cm-1 |
I-338 | m.p.120-121℃1HNMR(CDCl3)δ3.13(s,3H),3.50(s,3H),3.78(s,3H),5.08(s,1H),5.20(s,2H),6.90(m,2H),7.09(s,1H),7.15-7.19(m,3H),7.37-7.50(m,5H),7.56(dd,J=10.8,2.1Hz,1H),7.64(d,J=2.4Hz,1H),9.90(s,1H)IR(KBr)3460,2934,1694,1609,1585,1518,1467,1442,1348,1295,1273,1255,1238,1171,1123,1075,1003,960,828,807,755,700,653,582,522cm-1 |
I-339 | m.p.256-258℃1HNMR(DMSO-d6)δ3.34(s,3H),3.35(s,3H),3.72(s,3H),5.28(s,2H),6.75(d,J=8.1Hz,2H),7.05-7.11(m,3H),7.36-7.45(m,4H),7.53(d,J=8.1Hz,2H),7.60-7.66(m,2H),9.44(s,1H),12.84(s,1H)IR(KBr)3459,2940,2563,1706,1612,1522,1469,1349,1294,1258,1185,1114,1082,1063,1000,961,919,827,756,699,524cm-1 |
I-340 | m.p.165-166℃1HNMR(CDCl3)δ3.14(s,3H),3.19(s,3H),3.51(s,3H),3.76(s,3H),5.21(s,2H),7.11(s,1H),7.17(d,J=8.4Hz,1H),7.29-7.50(m,9H),7.57(dd,J=8.1,2.1Hz,1H),7.65(d,J=2.1Hz,1H),10.02(s,1H)IR(CHCl3)2938,2844,1698,1613,1590,1515,1469,1372,1331,1293,1255,1174,1150,1122,1092,1005,969,873,816cm-1 |
I-341 | m.p.195-197℃1HNMR(CDCl3)δ3.13(s,3H),3.18(s,3H),347(s,3H),3.77(s,3H),5.20(s,2H),6.97(s,1H),7.17(d,J=8.7Hz,1H),7.30-7.50(m,9H),7.58(dd,J=8.7,1.8Hz,1H),7 67(d,J=1.8Hz,1H)IR(CHCl3)2938,1740,1707,1601,1516,1472,1371,1293,1260,1174,1149,1117,1082,1060,1002,971,875cm-1 |
I-342 | m.p.207-209℃1HNMR(CD3OD)δ3.40(s,3H),3.72(s,3H),5.21(s,2H),6.76-6.78(m,2H),6.97(s,1H),7.01-7.17(m,4H),7.31-7.52(m,6H)IR(KBr)3366,1705,1612,1591,1522,1473,1434,1375,1253,1234,1130,1084,1061,998,918,864,835,813,792,743,697,648,526cm-1 |
I-343 | m.p.206-208℃1H NMR(CDCl3)δ3.14(s,3H),3.48(s,3H),3.72(s,3H),5.20(s,2H),5.48(br,1H),6.85-6.89(m,3H),7.15-7.19(m,3H),7.37-7.51(m,8H),7.56(dd,J=8.4,2 4Hz,1H),7.68(d,J=2.4Hz,1H)IR(CHCl3)3320,2938,1612,1520,1474,1371,1292,1257,1172,1120,1090,1005,972,857,837,818cm-1 |
I-344 | m.p.187-190℃1HNMR(CDCl3)δ2.33(s,3H),3.13(s,3H),3.50(s,3H),3.76(s,3H),5.20(s,2H),7.10(s,1H),7.15-7.19(m,3H),7.28-7.50(m,7H),7.56(dd,J=8.7,2.4Hz,1H),7.64(d,J=2.4Hz,1H),9.93(s,1H)IR(CHCl3)2930,2836,1750,1695,1588,1513,1465,1369,1329,1220,1166,1122,1091,1003,962,912,848,813cm-1 |
I-345 | m.p.218-220℃1HNMR(DMSO-d6)δ2.29(s,3H),3.36(s,3H),3.37(s,3H),3.76(s,3H),5.29(s,2H),7.11-7.16(m,3H),7.31-7.46(m,6H),7.52-7.55(m,2H),7.62-7.68(m,2H),13.00(br,1H)IR(KBr)3433,2940,2600,1757,1713,1652,1611,1518,1471,1365,1295,1260,1216,1200,1171,1117,1082,1061,1022,998,975,916,897,829,804,735,697,525cm-1 |
I-346 | m.p.206-208℃1HNMR(CDCL3)δ2.31(s,3H),3.13(s,3H),3.45(s,3H),3.58(s,3H),3.76(s,3H),5.19(s,2H),6.95(s,1H),7.08-7.16(m,3H),7.34-7.50(m,7H),7.57(dd,J=8.7,2.4Hz,1H),7.67(d,J=2.4Hz,1H)IR(CHCl3)2939,1732,1613,1599,1518,1468,1371,1290,1169,1117,1081,1064,1004,972,961,905,847,828cm-1 |
I-347 | m.p.201-203℃1HNMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),3.34(s,3H),3.63(s,3H),4.51(d,J=4.2Hz,2H),5.49(t,J=4.6Hz,1H),6.66(s,1H),6.76(s,2H),6.86(s,1H),7.23-7.29(m,2H),7.62-7.66(m,2H)IR(KBr)3431,2935,1575,1516,1462,1444,1421,1397,1375,1224,1159,1063,837cm-1 |
I-348 | m.p.265-266℃1HNMR(DMSO-d6)δ2.31(s,3H),3.33(s,3H),3.62(s,3H),5.03(s,2H),6.66(s,1H),6.72-6.90(m,4H),7.18-7.28(m,3H),7.38(d,J=5.2Hz,2H),7.64(dd,J=4.0,5.4Hz,2H)IR(KBr)3428,2925,1575,1516,1463,1442,1396,1374,1248,1221,1129,1087,1068cm-1 |
I-349 | m.p.262-263℃1HNMR(DMSO-d6)δ1.64(s,3H),1.70(s,3H),2.43(dt,J=4.6,5.0Hz,2H),3.34(s,3H),3.62(s,3H),3.91(t,J=4.8Hz,2H),5.25(t,J=4.6Hz,1H),6.70(s,1H),6.75(s,2H),6.87(s,1H),7.23-7.29(m,2H),7.64(dd,J=2.0,5.8Hz,2H)IR(KBr)3430,2934,1575,1516,1464,1443,1422,1398,1375,14246,1225,1065,1015cm-1 |
I-350 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(d,J=0.6Hz,3H),2.54(s,3H),2.73(s,3H),3.23(s,3H),3.54(s,3H),3.77(s,3H),4.63(d,J=6.6Hz,2H),5.49(m,1H),6.85(s,1H),7.09(d,J=8.4Hz,1H),7.30-7.40(m,4H),7.53-7.59(m,2H)IR(CHCl3)2936,1606,1515,1475,1366,1116,1078,970,875,820cm-1 |
I-351 | 1HNMR(CDCl3)δ1.68(s,3H),1.74(d,J=0.9Hz,3H),2.48-2.60(m,5H),2.75(s,3H),3.21(s,3H),3.54(s,3H),3.77(s,3H),4.07(t,J=6.9Hz,2H),5.21(m,1H),6.85(s,1H),7.07(d,J=8.7Hz,1H),7.30-7.42(m,4H),7.53-7.59(m,2H)IR(CHCl3)2928,1607,1517,1476,1367,1267,1118,1080,1014,971,892,822cm-1 |
I-352 | m.p.201-203℃1HNMR(CDCl3)δ3.35(s,3H),3.75(s,3H),3.76(s,3H),5.26(s,2H),6.79-6.83(m,2H),6.97(s,1H),7.01(s,1H),7.31-7.54(m,10H),9.45(s,1H)IR(KBr)3600-2800(br),1610,1525,1492,1462,1377,1337,1298,1208,1171,1114,1054,1031cm-1 |
I-353 | m.p.141-143℃1HNMR(CDCl3)δ3.56(s,3H),3.78(s,3H),3.80(s,3H),4.86(s,1H),5.26(s,2H),6.88-6.92(m,2H),6.92(s,1H),6.93(s,1H),7.24-7.29(m,2H),7.36-7.41(m,1H),7.45-7.50(m,2H)IR(KBr)3600-2800(br),1612,1524,1491,1463,1448,1378,1263,1205,1177,1153,1071,1053,1026cm-1 |
I-354 | m.p.115-115.5℃1HNMR(CDCl3)δ3.19(s,3H),3.56(s,3H),3.79(s,3H),3.80(s,3H),5.27(s,2H),6.93(s,1H),6.94(s,1H),7.25-7.27(m,2H),7.32-7.40(m,3H),7.60-7.64(m,2H)IR(KBr)3600-2800(br),1524,1492,1463,1379,1266,1210,1174,1154,1126,1082,1053,1029cm-1 |
I-355 | m.p.139-140℃1HNMR(CDCl3)δ1.77(d,J=0.6Hz,3H),1.81(d,J=0.9Hz,3H),3.82(s,6H),4.64(d,J=6.9Hz,2H),5.52-5.57(m,1H),6.95(s,1H),6.97(s,1H),7.04(t,J=8.4Hz,1H),7.26-7.31(m,1H),7.37(dd,J=2.1,12.6Hz,1H),7.73-7.77(m,2H),8.26-8.31(m,2H)IR(KBr)3600-2800(br),1593,1524,1508,1486,1464,1380,1355,1278,1264,1211,1054,1029cm-1 |
I-356 | 泡沫1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.53(s,3H),3.78(s,3H),5.19(s,2H),6.83(s,1H),7.10-7.19(m,3H),7.30-7.50(m,7H),7.56-7.64(m,2H)IR(KBr)1607,1520,1482,1365,1232,1177,1119,1082,1013cm-1 |
I-357 | 1HNMR(CDCl3)δ2.39(s,3H),3.48(s,3H),3.75(s,3H),5.11(s,2H),5.67(s,1H),5.88(s,1H),6.46(s,1H),6.95(d.d,J=8.7&1.8Hz,1H),7.02-7.11(m,1H),7.03(d,J=8.7Hz,1H),7.07(d,J=1.8Hz,1H),7.22(d,J=8.7Hz,2H),7.34(d,J=8.7Hz,2H),7.36-7.47(m,3H)IR(KBr)3546,3511,1611,1586,1517,1478,1405,1360,1318,1240,1109,1068,1007cm-1 |
I-358 | 1HNMR(CDCl3)δ3.03(s,6H),3.48(s,3H),3.77(s,3H),5.15(s,2H),5.71(s,1H),6.73(dd,J=8.7&1.8Hz,1H),6.82(d,J=8.4Hz,2H),6.97(d,J=1.8Hz,1H),6.98(dJ=8.7Hz,1H),7.11(s,1H),7.33-7.48(m,5H),7.56(d,J=8.7Hz,2H),9.92(s,1H)IR(KBr)3524,3447,1697,1612,1586,1525,1468,1364,1283,1257,1230,1201,1127,1103,1073,1020cm-1 |
I-359 | 1HNMR(CDCl3)δ3.04(s,6H),3.14(s,3H),3.48(s,3H),3.76(s,3H),5.17(s,2H),6.84(d,J=8.7Hz,2H),7.06-7.17(m,3H),7.34(d,J=1.8Hz,1H),7.35-7.50(m,6H),7.55(d,J=8.7Hz,2H),10.08(s,1H)IR(KBr)1698,1610,1527,1470,1357,1290,1232,1183,1115,1083,1018cm-1 |
I-360 | 1HNMR(CDCl3)δ2.56(s,3H),3.02(s,6H),3.54(s,3H),3.76(s,3H),5.16(s,2H),5.67(s,1H),6.80(d,J=8.4Hz,2H),6.85(s,1H),6.91(d.d,J=8.4&2.1Hz,1H),7.01(d,J=8.4Hz,1H),7.05(d,J=2.1Hz,1H),7.30-7.47(m,5H),7.55(d,J=8.7Hz,2H)IR(KBr)3542,3436,1605,1530,1483,1391,1360,1287,1253,1234,1169,1074,1016cm-1 |
I-361 | 1HNMR(CDCl3)δ1.31(d,J=6.9Hz,6H),2.57(s,3H),2.97(quint,J=6.9Hz,1H),3.54(s,3H),3.76(s,3H),5.17(s,2H),5.68(s,1H),6.86(s,1H),6.92(dd,J=8.4&2.1Hz,1H),7.02(d,J=8.4Hz,1H),7.05(d,J=2.1Hz,1H),7.31(d,J=8.1Hz,2H),7.34-7.46(m,5H),7.55(d,J=8.1Hz,2H)IR(KBr)3446,1606,1585,1522,1484,1457,1394,1356,1289,1257,1228,1172,1076,1018,1007cm-1 |
I-362 | 1HNMR(CDCl3)δ1.31(d,J=6.9Hz,6H),2.98(quint,J=6.9Hz,1H),3.46(s,3H),3.74(s,3H),5.15(s,2H),5.67(s,1H),5.92(s,1H),6.48(s,1H),6.97(dd,J=8.4&1.8Hz,1H),7.03(d,J=8.4Hz,1H),7.10(d,J=1.8Hz,1H),7.25(s,1H),7.31(d,J=7.8Hz,2H),7.34-7.49(m,5H),7.57(d,J=7.8Hz,2H)IR(KBr)3538,3505,3465,1610,1586,1552,1518,1584,1458,1398,1281,1288,1245,1198,1112,1071,1002cm-1 |
I-363 | 1HNMR(CDCl3)δ2.66(s,3H),3.06(s,3H),3.13(s,3H),3.57(s,3H),3.67(s,3H),3.78(s,3H),5.19(s,2H),6.44(s,1H),6.85(s,1H),7.15(d,J=8.7Hz,1H),7.28-7.51(m,10H)IR(KBr)3443,1604,1518,1479,1364,1237,1177,1153,1118,1078,1014cm-1 |
I-364 | 1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.70(s,3H),3.06(s,3H),3.24(s,3H),3.58(s,3H),3.78(s,3H),4.64(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),6.42(s,1H),6.85(s,1H),7.09(d,J=8.4Hz,1H),7.28-7.49(m,5H)IR(KBr)3432,3285,1604,1518,1479,1364,1328,1291,1269,1237,1177,1154,1117,1078cm-1 |
I-365 | 1HNMR(CDCl3)δ1.57(s,3H),1.67(s,3H),1.77(s,3H),1.81(s,3H),2.70(s,3H),2.96(s,3H),3.24(s,3H),3.53(s,3H),3.78(s,3H),4.32(d,J=7.2Hz,2H),4.64(d,J=6.9Hz,2H),5.25(t,J=6.9Hz,1H),5.49(t,J=7.2Hz,1H),6.85(s,1H),7.09(d,J=8.7Hz,1H),7.31-7.41(m,3H),7.44-7.64(m,3H)IR(KBr)3433,1600,1517,1474,1365,1339,1237,1178,1153,1118,1078,1014cm-1 |
I-366 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.08(s,3H),348(s,3H),3.75(s,3H),4.62(d,J=7.2Hz,2H),5.54(t,J=7.2Hz,1H),5.70(s,1H),5.85(s,1H),6.40(s,1H),6.46(s,1H),6 89-7.00(m,2H),7.05(d,J=1.5Hz,1H),7.43-7.51(m,3H)IR(KBr)3437,1605,1585,1518,1482,1386,1323,1243,1152,1114,1071,1002cm-1 |
I-367 | 1HNMR(CDCl3)δ2.37(s,3H),3.21(s,3H),3.47(s,3H),3 64(s,3H),3.77(s,3H),3.84(s,3H),5.17(s,2H),6.63(s,1H),6.78(s,1H),7.10(s,1H),7.20(d,J=8.1Hz,2H),7.40(d,J=8.1Hz,2H),7.41(d,J=9.3Hz,2H),7.70(d,J=9.3Hz,2H)IR(KBr)1702,1607,1589,1518,1468,1356,1216,1151,1067,1039,1018cm-1 |
I-368 | 1HNMR(CDCl3)δ2.37(s,3H),3.21(s,3H),3.48(s,6H),3.65(s,3H),3.73(s,3H),3.83(s,3H),4.32(d,J=11.4Hz,1H),4.51(d,J=11.4Hz,1H),5.17(s,2H),6.93(s,1H),6.71(s,1H),6.88(s,1H),7.21(d,J=8.4Hz,2H),7.32-7.41(m,4H),7.73(d,J=8.4Hz,2H)IR(KBr)3514,1608,1516,1465,1355,1215,1119,1076,1039,1017cm-1 |
I-369 | m.p.125-127℃1HNMR(CDCl3)δ2.60(s,3H),3.52(s,3H),3.73(s,3H),3.84(s,3H),5.20(s,2H),6.83(s,1H),7.00-7.48(m,12H)IR(KBr)3434,2943,1611,1580,1520,1498,1480,1398,1297,1268,1245,1179,1129,1079,1009cm-1 |
I-370 | m.p.137-139℃1HNMR(CDCl3)δ3.43(s,3H),3.71(s,3H),3.85(s,3H),5.19(s,2H),5.92(s,1H),6.43(s,1H),7.01-7.51(m,12H)lR(KBr)3391,2937,1615,1583,1520,1503,1482,1464,1405,1359,1314,1292,1273,1239,1121,1108,1069,1005cm-1 |
I-371 | m.p.92-94℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.70(s,3H),3.53(s,3H),3.73(s,3H),3.84(s,3H),4.63(d,J=6.9Hz,2H),5.53(m,1H),6.84(s,1H),7.00-7.45(m,7H)IR(KBr)3433,2938,1609,1581,1523,1499,1480,1401,1368,1297,1268,1240,1178,1118,1079,1021cm-1 |
I-372 | 泡沫1HNMR(CDCl3)δ1.68(s,3H),1.74(d,J=0.6Hz,3H),2.50-2.59(m,2H),2.71(s,3H),3.53(s,3H),3.73(s,3H),3.84(s,3H),4.04(t,J=7.2Hz,2H),5.23(m,1H),6.83(s,1H),7.00-7.42(m,7H)IR(CHCl3)3011,2938,1612,1581,1522,1500,1480,1465,1398,1370,1301,1268,1238,1209,1176,1119,1081,1017cm-1 |
I-373 | m.p.95-98℃1HNMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.43(s,3H),3.72(s,3H),3.85(s,3H),4.63(d,J=6.6Hz,2H),5.56(m,1H),5.92(s,1H),6.43(s,1H),7.01-7.42(m,7H)IR(KBr)3318,2937,1612,1598,1500,1485,1464,1450,1361,1298,1275,1240,1104,1072,1011cm-1 |
I-374 | m.p.69-71℃1HNMR(CDCl3)δ1.68(s,3H),1.74(d,J=0.6Hz,3H),2.50-2.60(m,2H),3.43(s,3H),3.71(s,3H),3.85(s,3H),4.04(t,J=7.2Hz,2H),5.23(m,1H),5.91(s,1H),6.43(s,1H),7.00-7.42(m,7H)IR(KBr)3385,2933,1611,1583,1521,1503,1485,1466,1403,1358,1299,1276,1241,1122,1104,1071,1011cm-1 |
I-375 | m.p.105-107℃1HNMR(CDCl3)δ2.36(s,3H),2.59(s,3H),3.52(s,3H),3.73(s,3H),3.84(s,3H),5.16(s,2H),6.83(s,1H),7.00-7.42(m,11H)IR(KBr)3433,2940,1609,1581,1522,1499,1481,1461,1401,1366,1296,1269,1240,1178,1117,1079,1021,1011cm-1 |
I-376 | m.p.142-144℃1HNMR(CDCl3)δ2.37(s,3H),3.42(s,3H),3.71(s,3H),3.85(s,3H),5.14(s,2H),5.91(s,1H),6.43(s,1H),7.01-7.42(m,11H)IR(KBr)3367,2936,1615,1583,1520,1502,1482,1464,1447,1405,1359,1317,1291,1274,1239,1121,1109,1070,1009cm-1 |
I-377 | m.p.174-176℃1HNMR(CDCl3)δ3.21(s,3H),3.41(s,3H),3.63(s,3H),3.77(s,3H),5.30(s,2H),6.94(s,1H),7.03-7.05(m,2H),7.15-7.20(m,1H),7.25(m,1H),7.38(d,J=8.9Hz,2H),7.62(d,J=7.8Hz,1H),7.71(d,J=8.9Hz,2H),7.76(dt,J=7.8,1.5Hz,1H),8.60(m,1H)IR(KBr)1732,1523,1474,1368,1148,1061,863,845,790cm-1 |
I-378 | m.p.>260℃1HNMR(DMSO-d6)δ3.32(s,3H),3.73(s,3H),5.28(s,2H),6.87(d,J=8.7Hz,2H),7.00(s,1H),7.04(dd,J=8.9,1.8Hz,1H),7.16(dd,J=12.3,1.8Hz,1H),7.26(t,J=8.9Hz,1H),7.39(m,1H),7.57(d,J=8.7Hz,2H),7.58(d,J=7,8Hz,1H),7.89(dt,J=7.8,1.5Hz,1H),8.61(m,1H),9.61(s,1H),12.9(brs,1H)IR(KBr)3383,1735,1705,1610,1522,1471,1272,1226,1059,1014,838,762cm-1 |
I-379 | m.p.137-138℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.46(s,3H),3.79(s,3H),4.64(d,J=4.6Hz,1H),5.56(t,J=4.6Hz,1H),6.92-7.20(m,6H),7.61(dd,J=3.6,5.8Hz,2H),9.96(Brs,1H)IR(KBr)3434,2966 2935,2839,1702,1695,1521,1466,1378,1299,1287,1272,1240,1012,840cm-1 |
I-380 | m.p.98-99℃1HNMR(CDCl3)δ2.37(s,3H),3.45(s,3H),3.78(s,3H),5.15(s,2H),6.93-7.26(m,4H),7.36(d,J=7.8Hz,2H),7.62(dd,J=4.0,8.8Hz,2H ),9.94(s,1H)IR(KBr)3446,2933,2845,1699,1521,1473,1463,1381,1293,1261,1238,1221,1131,803cm-1 |
I-381 | m.p.118-119℃1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.54(dt,J=5.0,7.8Hz,2H),3.45(s,3H),3.78(s,3H),4.05(t,J=7.2Hz,2H),5.24(t,J=4.4Hz,1H),6.95-7.16(m,6H),7.61(dd,J=3.4,8.8Hz,2H),9.95(brs,1H)IR(KBr)3433,2959,2930,2842,1701,1602,1522,1464,1379,1303,1263,1222,1132,1018cm-1 |
I-382 | m.p.93-94℃1HNMR(DMSO-d6)δ1.74(s,3H),1.78(s,3H),3.32(s,3H),3.71(s,3H),4.62(d,J=7.0Hz,2H),5.48(t,J=5.8Hz,1H),6.91(s,1H),7.09-7.35(m,2H),7.64-7.71(m,2H)IR(KBr)3433,2976,2937,1707,1604,1520,1472,1376,1300,1265,1226,1160,1131,1060,839cm-1 |
I-383 | m.p.98-99℃1HNMR(DMSO-d6)δ2.32(s,3H),3.31(s,3H),3.70(s,3H),5.13(s,2H),6.88(s,1H),7.14-7.39(m,5H),7.63-7.70(m,2H)IR(KBr)3433,2981,2937,1704,1603,1520,1470,1375,1301,1266,1226,1159,1061,839cm-1 |
I-384 | 油状物1HNMR(DMSO-d6)δ1.68(s,3H),1.74(s,3H),2.48-2.56(m,2H),3.57(s,3H),3.77(s,3H),3.98(t,J=4.8Hz,2H),5.26(t,J=4.2Hz,1H),6.84(s,1H),7.05-7.36(m,5H),7.63-7.70(m,2H)IR(KBr)3433,2979,2938,1726,1603,1522,1470,1376,1301,1264,1226,1160,1132,1080,1058,840cm-1 |
I-385 | m.p.137-138℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.55(s,3H),3.21(s,3H),3.57(s,3H),3.78(s,3H),4.56(d,J=7.0Hz,2H),5.52(t,J=7.4Hz,1H),6.84(s,1H),7.02(d,J=8.8Hz,2H),7.34-7.40(m,4H),7.70(d,J=8.8Hz,2H)IR(KBr)3434,2938,1607,1519,1366,1244,1174,1151,1072,871,796cm-1 |
I-386 | m.p.169-170℃1HNMR(CDCl3)δ2.48(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),5.08(s,2H),6.84(s,1H),7.07(d,J=5.8Hz,2H),7.19-7.39(m,4H),7.70(d,J=6.0Hz,2H)IR(KBr)3432,3016,2935,1605,1519,1479,1368,1357,1233,1176,1151,1076,876,843,798cm-1 |
I-387 | m.p.140-141℃1HNMR(CDCl3)δ1.68(s,3H),1.75(s,3H),2.51(dt,J=4.4,4.6Hz,2H),2.55(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),3.97(t,J=4.8Hz,2H),5.26(t,J=4.0Hz,1H),6.84(s,1H),6.99(d,J=5.8Hz,2H),7.34-7.39(m,4H),7.70(d,J=5.8Hz,2H)IR(KBr)3445,2937,1608,1519,1480,1391,1361,1351,1237,1177,1154,1077,962,871,862,800cm-1 |
I-388 | m.p.124-125℃1HNMR(DMSO-d6)δ1.73(s,3H),1.75(s,3H),3.30(s,3H),3.65(s,3H),4.54(d,J=6.6Hz,2H),5.47(t,J=6.4Hz,1H),6.40(s,1H),6.82-6.94(m,4H),7.20(d,J=8.6Hz,2H),7.44(d,J=8.2Hz,2H)IR(KBr)3411,2934,1608,1523,1487,1396,1231,1175,1105,1072,996,898cm-1 |
I-389 | m.p.93-94℃1HNMR(DMSO-d6)δ2.32(s,3H),3.32(s,3H),3.64(s,3H),5.08(s,2H),6.40(s,1H),6.84(d,J=8.6Hz,2H),6.98(d,J=8.6Hz,2H),7.19-7.23(m,4H),7.34-7.46(m,4H)IR(KBr)3398,2933,1609,1523,1486,1461,1398,1235,1174,1119,1071,997,829cm-1 |
I-390 | 油状物1HNMR(DMSO-d6)δ1.72(s,3H),1.74(s,3H),2.52(dt,J=4.8,5.0Hz,2H),3.24(s,3H),3.58(s,3H),4.06(t,J=7.2Hz,2H),5.24(t,J=4.4Hz,1H),6.80-6.95(m,4H),7.22(d,J=8.4Hz,2H),7.46(d,J=8.2Hz,2H)IR(KBr)3340,2934,1608,1522,1486,1396,1285,1230,1175,1106,1072,996,828cm-1 |
I-391 | 1HNMR(CDCl3+CD3OD)δ3.05(s,3H),3.48(s,3H),3.75(s,3H),5.16(s,2H),5.97(s,1H),6.02(s,1H),6.47(s,1H),6.94(d.d,J=8.4&1.8Hz,1H),7.04(d,J=8.4Hz,1H),7.07(d,J=1.8Hz,1H),7.22-7.52(m,9H)IR(KBr)3548,3357,1603,1589,1520,1487,1460,1445,1410,1329,1286,1247,1153,1115,1077,1010cm-1 |
I-392 | 1HNMR(CDCl3)δ2.37(s,3H),2.77-2.88(broad,1H),3.47(s,3H),3.64(s,3H),3.72(s,3H),3.82(s,3H),4.32(d.d,J=11.1&0.6Hz,1H),4.45-4.56(broad,1H),4.92(s,1H),5.16(s,2H),6.70(d,J=9.3Hz,2H),6.88(s,1H),6.92(d,J=9.0Hz,2H),7.22(d,J=8.4Hz,2H),7.38(d,J=8.4Hz,2H),7.56(d,J=9.0Hz,2H)IR(KBr)3476,1610,1519,1476,1463,1386,1265,1215,1074,1041,1010cm-1 |
I-393 | 泡沫1HNMR(CD3OD)δ2.34(s,3H),3.38(s,3H),3.68(s,3H),4.00(dd,J=9.9,8.7Hz,1H),4.17(dd,J=9.9,3.0Hz,1H),5.06(dd,J=8.7,3.0Hz,1H),6.43(s,1H),6.78(dd,J=8.7,1.8,1H),6.86(d,J=8.7Hz,2H),6.88(d,J=1.8Hz,1H),6.91(d,J=8.4Hz,1H),7.20(d,J=8.1Hz,2H),7.36(d,J=8.1Hz,2H),7.46(d,J=8.7Hz,2H)IR(Nujol)3367,1655,1612,1586,1523,1489,1459,1254,1225,1115,1072,1015,941,817cm-1 |
I-394 | 泡沫1HNMR(CD3OD)δ3.38(s,3H),3.67(s,3H),4.02(dd,J=10.2,9.0Hz,1H),4.20(dd,J=10.2,3.3Hz,1H),5.11(dd,J=9.0,3.3Hz,1H),6.43(s,1H),6.78(dd,J=8.4,2.1,1H),6.85(d,J=8.7Hz,2H),6.88(d,J=2.1Hz,1H),6.91(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H),7.30~7.50(m,5H)IR(Nujol)3368,1655,1612,1587,1523,1489,1456,1254,1225,1114,1072,1014,941,825,764cm-1 |
I-395 | 泡沫1HNMR(CDCl3)δ2.48(s,3H),2.82(s,3H),3.16(s,3H),3.22(s,3H),3.54(s,3H),3.77(s,3H),6.85(s,3H),7.34~7.38(m,2H),7.38(d,J=8.1Hz,2H),7.39(d,J=8.7Hz,2H),7.46(d,J=1.8Hz,1H),7.46(d,J=8.7Hz,2H),7.82(d,J=8.1Hz,2H)IR(Nujol)1597,1514,1479,1464,1177,1152,1085,969,883,846,797,729cm-1 |
I-396 | 泡沫1HNMR(CDCl3)δ2.85(s,3H),3.14(s,3H),3.22(s,3H),3.54(s,3H),3.77(s,3H),6.85(s,1H),7.36(m,2H),739(d,J=8.7Hz,2H),7.45,(m,1H),7.60(m,2H),7.66(d,J=8.7Hz,2H),7.74(m,1H),7.94(m,2H)IR(Nujol)1612,1584,1514,1479,1451,1179,1152,1085,969,949,846,797,737cm-1 |
I-397 | 泡沫1HNMR(CDCl3)δ2.73(s,3H),3.21(s,6H),3.55(s,3H),3.77(s,3H),5.20(s,2H),6.84(s,1H),7.16(brs,1H),7.22(d,J=8.1Hz,1H),7.33,(d,J=2.4Hz,1H),7.37(brs,2H),7.38(d,J=8.7Hz,2H),7.65(brs,1H),7.67(d,J=8.7Hz,2H)IR(Nujol)1608,1519,1480,1464,1176,1151,1080,972,876,846,798cm-1 |
I-398 | 泡沫1HNMR(CDCl3)δ2.91(s,3H),3.19(s,3H),3.22(s,3H),3.54(s,3H),3.78(s,3H),5.26(s,2H),5.34(s,2H),7.04(brs,1H),7.05(s,2H),7.12(brs,1H),7.39(d,J=8.7Hz,2H),7.36~7.43(m,3H),7.67(d,J=8.7Hz,2H)IR(Nujol)1608,1519,1480,1463,1176,1151,1079,972,876,799cm-1 |
I-399 | m.p.203-205℃1HNMR(DMSO-d6)δ2.87(s,3H),3.35(s,3H),3.45(s,3H),3.52(s,3H),3.78(s,3H),5.39(s,2H),7.07(s,1H),7.08(d,J=3.9Hz,1H),7.16(d,J=3.9Hz,1H),7.31(dd,J=9.0,1.8Hz,1H),7.33(s,1H),7.42(d,J=9.0Hz,1H),7.49(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)1609,1520,1481,1455,1231,1080,1013,984,947,878,832,798cm-1 |
I-400 | 泡沫1HNMR(CDCl3)δ2.72(s,3H),3.14(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),5.14(s,2H),6.84(s,1H),7.11(d,J=8.7Hz,1H),7.34(dd,J=2.1,8.7Hz,1H),7.34(d,J=8.4Hz,2H),7.37(d,J=8.4Hz,2H),7.41(d,J=2.1Hz,1H),7.54(d,J=8.4Hz,2H),7.68(d,J=8.4Hz,2H) |
I-401 | 泡沫1HNMR(CDCl3)δ2.83(s,3H),3.14(s,3H),3.22(s,3H),3.55(s,3H),3.78(s,3H),5.26(s,2H),6.85(s,1H),7.24(d,J=8.4Hz,1H),7.38(d,J=8.4Hz,1H),7.41(dd,J=2.1,8.4Hz,1H),7.44(d,J=2.1Hz,1H),7.67(d,J=8.4Hz,2H)IR(KBr)1609,1523,1509,1481,1367,1402,1178,1152,1080,973,943,876,798cm-1 |
I-402 | 泡沫1HNMR(CDCl3)δ2.68(s,3H),3.14(s,3H),3.21(s,3H),3.55(s,3H),3.66(s,2H),3.71(s,3H),3.78(s,3H),5.18(s,2H),6.84(s,1H),7.14(d,J=8.4Hz,1H),7 32(d,J=8.7Hz,1H),7.35(dd,J=2.1,8.7Hz,1H),7.37(d,J=8.4Hz,2H),7.39(d,J=2.1Hz,1H),7.42(d,J=8.4Hz,2H),7.67(d,J=8.4Hz,2H)IR(KBr)1736,1610,1519,1481,1365,1177,1151,1079,876,817,798cm-1 |
I-403 | 泡沫1HNMR(CDCl3)δ2.70(s,3H),3.16(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.24(s,2H),6.84(s,1H),7.18(d,J=8.4Hz,1H),7.36(dd,J=1.5,8.4Hz,1H),7.38(d,J=8.4Hz,2H),7.41(d,J=1.5Hz,1H),7.46(m,2H),7.54(d,J=8.1Hz,2H),7.62(m,3H),7.64(d,J=8.1Hz,2H),7.68(d,J=8.4Hz,2H)IR(KBr)1609,1519,1481,1365,1177,1151,1079,1014,876,818,797cm-1 |
I-404 | m.p.128-130℃1HNMR(CDCl3)δ2.75(s,3H),2.92(s,3H),3.18(t,J=6.9Hz,2H),3.21(s,3H),3.55(s,3H),3.77(s,3H),4.34(t,J=6.9Hz,2H),6.81(s,1H),7.08(d,J=8.4Hz,1H),7.29(m,2H),7.32(br.s,3H),7.35(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.4Hz,2H),7.39(d,J=2.1Hz,1H),7.67(d,J=8.4Hz,2H)IR(KBr)1609,1520,1481,1364,1177,1151,1080,872,815,797cm-1 |
I-405 | 泡沫1HNMR(CDCl3)δ1.71(d,J=6.3Hz,3H),2.45(br.s,3H),3.20(s,3H),3.28(s,3H),3.53(s,3H),3.75(s,3H),5.43(q,J=6.3Hz,1H),6.81(s,1H),6,90(d,J=8.4Hz,1H),7.16(dd,J=2.1,8.4Hz,1H),7.30(m,1H),7.36(d,J=2.1Hz,1H),7.37(d,J=8.4Hz,2H),7.35-7.41(m,4H),7.66(d,J=8.4Hz,2H)IR(KBr)1609,1518,1480,1365,1177,1151,1078,874,818,798cm-1 |
I-406 | 泡沫1HNMR(CDCl3)δ1.02(t,J=9.0Hz,3H),2.04(dq,=6.3,9.0Hz,2H),2.39(brs,3H),3.20(s,3H),3.30(s,3H),3.53(s,3H),3.75(s,3H),5.18(t,J=6.3Hz,1H),6.80(s,1H),6.88(d,J=8.4Hz,1H),6.92(m,1H),7.14(dd,J=2.4,8.4Hz,1H),7.25-7.40(m,7H),7.66(d,J=8.4Hz,2H)IR(KBr)1609,1518,1480,135,1177,1151,1079,874,819,797cm-1 |
I-407 | 泡沫1HNMR(CDCl3)δ2.46(s,3H),3.07(s,3H),3.20(s,3H),3.54(s,3H),3.76(s,3H),6.33(s,1H),6.82(s,1H),6.99(d,J=9.0Hz,1H),7.19(dd,J=2.1,9.0Hz,1H),7.26-7.40(m,9H),7.43-7.47(m,4H),7.66(d,J=8.4Hz,2H)IR(KBr)1607,1518,1481,1364,1177,1151,1081,873,822,798cm-1 |
I-408 | m.p.179-180℃1HNMR(CDCl3)δ1.69(d,J=6.3Hz,3H),2.34(br.s,3H),2.45(s,3H),3.20(s,3H),3.27(s,3H),3.54(s,3H),3.75(s,3H),5.40(q,J=6.3Hz,1H),6.81(s,1H),6.92(d,J=8.7Hz,1H),7.15(d,J=8.7Hz,2H),7.16(dd,J=2.1,8.4Hz,1H),7.27(d,J=8.7Hz,1H),7.35(d,J=2.1Hz,1H),7.37(d,J=8.4Hz,2H),7.66(d,J=8.4Hz,2H)IR(KBr)1609,1518,1480,1365,1177,1151,1078,874,819,797cm-1 |
I-409 | m.p.243-244℃1HNMR(DMSO-d6)δ3.30(s,3H),3.64(s,3H),5.19(s,2H),6.39(s,1H),6.64(dd,J=1.8,8.4Hz,1H),6.77(d,J=1.8Hz,1H),6.83(d,J=8.4Hz,2H),6.97(d,J=8.4Hz,1H),7.37(t,J=7.5Hz,1H),7.44(d,J=8.4Hz,2H),7.48(t,J=8.4Hz,2H),7.60(d,J=8.4Hz,2H),7.67-7.73(m,5H)IR(KBr)3421,1610,1523,1488,1463,1403,1176,1115,1072,821cm-1 |
I-410 | 泡沫1HNMR(CDCl3)δ3.18(t,J=6.9Hz,2H),3.45(s,3H),3.73(s,3H),4.31(t,J=6.9Hz,2H),6.44(s,1H),6.91(d,J=8.4Hz,2H),6.94(br.s,2H),7.03(br.s,1H),7.23-7.37(m,5H),7.53(d,J=8.4Hz,2H)IR(KBr)3434,1612,1587,1523,1489,1455,1403,1250,1113,1070,1011,825,815cm-1 |
I-411 | 泡沫1HNMR(C1DCl3)δ1.70(d,J=6.0Hz,3H),3.44(s,3H),3.72(s,3H),5.36(q,J=6.0Hz,1H),6.42(s,1H),6.78(d,J=8.1Hz,1H),6.81(dd,J=1.5,8.7Hz,1H),6.91(d,J=8.4Hz,2H),7.06(d,J=1.5Hz,1H),7.26-7.42(m,4),7.51(d,J=8.dHz,2H)IR(KBr)3472,1612,1587,1523,1488,1454,1403,1248,1113,1070,1011,825,cm-1 |
I-412 | 泡沫1HNMR(CDCl3)δ1.03(t,J=7.2Hz,3H),1.94(m,1H),2.06(m,1H),3.43(s,3H),3.72(s,3H),5.08(dd,J=7.2,5.4Hz,1H),6.43(s,1H),6.73(d,J=8.4Hz,1H),6.78(dd,J=1.8,8.4Hz,1H),6.90(d,J=8.4Hz,2H),7.05(d,J=1.8Hz,1H),7.25-7.38(m,5H),7.51(d,J=8.4Hz,2H)IR(KBr)3434,1612,1522,1488,1454,1403,1247,1113,1070,1011,826,811cm-1 |
I-413 | 泡沫1HNMR(CDCl3)δ3.44(s,3H),3.73(s,3H),6.25(s,1H),6.43(s,1H),7.26(m,2H),6.90(d,J=8.4Hz,2H),7.08(d,J=2.1Hz,1H),7.29-7.43(m,10H),7.51(d,J=8.4Hz,2H)IR(KBr)3432,1611,1523,1489,1454,1402,1226,1110,1069,1011,825cm-1 |
I-414 | 泡沫1HNMR(CDCl3)δ1.69(d,J=6.3Hz,3H),2.35(s,3H),3.44(s,3H),3.72(s,3H),5.33(q,J=6.3Hz,1H),6.42(s,1H),6.80(br.s,2H),6.90(d,J=8.4Hz,2H),7.05(br.s,1H),7.18(d,J=7.8Hz,2H),7.29(d,J=7.8Hz,2H),7.51(d,J=8.4Hz,2H)IR(KBr)3433,1612,1522,1488,1459,1403,1248,1113,1069,1011,817cm-1 |
I-415 | m.p.164-167℃1HNMR(CDCl3)δ3.79(s,3H),3.80(s,3H),4.81(brs,1H),5.29(s,2H),6.88-6.94(m,4H),7.16(d,J=8.7Hz,1H),7.32-7.52(m,7H),7.73(dd,J=2.1,8.7Hz,1H),8.10(d,J=2.1Hz,1H)IR(KBr)3513,2930,1618,1529,1497,1448,1387,1354,1296,1257,1211,1168,1091,1064,1024cm-1 |
I-416 | m.p.155-159℃1HNMR(CDCl3)δ3.20(s,3H),3.39(s,3H),3.82(s,3H),3.83(s,3H),6.95(s,1H),6.96(s,1H),7.34-7.38(m,2H),7.58-7.64(m,3H),7.87(dd,J=2.1,8.4Hz,1H),8.26(d,J=2.1Hz,1H)IR(KBr)3433,2944,1539,1519,1487,1358,1216,1176,1150,1086,1057,1031cm-1 |
I-417 | m.p.124-126℃1HNMR(CDCl3)δ3.19(s,3H),3.80(s,6H),5.30(s,2H),6.93(s,1H),6.94(s,1H),7.18(d,J=9.0Hz,1H),7.32-7.52(m,7H),7.59-7.64(m,2H),7.73(dd,J=2.1,9.0Hz,1H),8.10(d,J=2.1Hz,1H)IR(KBr)3433,2937,1619,1531,1491,1465,1450,1358,1290,1256,1211,1176,1150,1088,1062,1033cm-1 |
I-418 | m.p.151-153℃1HNMR(CDCl3)δ3.18(s,3H),3.781(s,3H),3.784(s,3H),5.14(s,2H),6.90-7.00(m,5H),7.31-7.50(m,7H),7.60-7.65(m,2H)IR(KBr)3480,3383,2930,1610,1523,1489,1467,1383,1358,1330,1211,1175,1147,1024cm-1 |
I-419 | m.p.198-200℃1HNMR(CDCl3)δ3.77(s,6H),5.13(s,2H),6.86-7.00(m,7H),7.34-7.50(m,7H)IR(KBr)3403,3327,1611,1592,1525,1492,1462,1444,1384,1318,1273,1243,1209,1178,1149,1110,1058,1037,1006cm-1 |
I-420 | m.p.168-171℃1HNMR(CDCl3)δ2.99(s,3H),3.19(s,3H),3.80(s,3H),3.81(s,3H),5.16(s,2H),6.83(brs,1H),6.92(s,1H),6.96(s,1H),7.06(d,J=8.7Hz,1H),7.32-7.46(m,8H),7.60-7.64(m,2H),7.81(d,J=2.1Hz,1H)IR(KBr)3403,3327,1611,1592,1525,1492,1462,1444,1384,1318,1273,1243,1209,1178,1149,1110,1058,1037,1006cm-1 |
I-421 | m.p.168-171℃1HNMR(CDCl3)δ3.19(s,3H),3.80(s,3H),3.81(s,3H),5.23(s,2H),6.93(s,1H),6.97(s,1H),7.07(d,J=8.7Hz,1H),7.33-7.45(m,8H),7.61-7.65(m,2H),8.58(d,J=2.4Hz,1H),8.66(brs,1H)IR(KBr)3401,1723,1613,1595,1549,1518,1486,1385,1365,1330,1299,1256,1212,1151,1119,1060,1037,1017cm-1 |
I-422 | m.p.159-160℃1HNMR(CDCl3)δ1.69(s,3H),1.74,(s,3H),2.55(q,J=7.2Hz,2H),2.73(s,3H),3.22(s,3H),3.55(s,3H),3.77(s,3H),4.06(t,J=7.2Hz,2H),5.24(t,J=7.2Hz,1H),6.85(s,1H),7.07(d,J=8.6Hz,1H),7.39(d,J=8.7Hz,2H),7.55(dd,J=8.6,2.1Hz,1H),7.63(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)1515,1481,1359,1325,1175,1140,1079,870,799cm-1 |
I-423 | m.p.180-182℃1HNMR(CDCl3)δ1.76(s,3H),1.81,(s,3H),2.71(s,3H),3.22(s,3H),3.55(s,3H),3.78(s,3H),4.06(d,J=6.3Hz,2H),5.50(t,J=6.3Hz,1H),6.85(s,1H),7.09(d,,J=8.7Hz,1H),7.39(d,J=8.7Hz,2H),7.55(dd,J=8.7,2.0Hz,1H),7.64(d,J=2.0Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)1514,1479,1360,1241,1174,1132,1078,866,800cm-1 |
I-424 | m.p.176-178℃1HNMR(CDCl3)δ2.64(s,3H),3.22(s,3H),3.55(s,3H),3.78(s,3H),5.26(s,2H),6.85(s,1H),7.14(d,J=8.6Hz,1H),7.33-7.48(m,7H),7.54(dd,J=8.6,2.1Hz,1H),7.66-7.70(m,3H)IR(KBr)1517,1482,1367,1327,1178,1150,1135,1081,878,797cm-1 |
I-425 | m.p.199-200℃1HNMR(CDCl3)δ2.37(s,3H),2.63(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.21(s,2H),6.84(s,1H),7.13(d,J=8.7Hz,1H),7.20(d,J=8.0Hz,2H),7.34(d,J=8.0Hz,2H),7.38(d,J=9.0Hz,2H),7.53(dd,J=8.7,1.8Hz,1H),7.66(d,J=1.8Hz,1H),7.68(d,J=9.0Hz,2H)IR(KBr)1517,1481,1366,1326,1255,1177,1151,1082,871,798cm-1 |
I-426 | 无定形1HNMR(CDCl3)δ1.68(s,3H),1.73(s,3H),2.54(q,J=7.2Hz,2H),3.44(s,3H),3.75(s,3H),4.05(t,J=7.2Hz,2H),5.07(s,1H),5.24(t,J=7.2Hz,1H),6.02(s,1H),6.45(s,1H),6.92(d,J=8.6Hz,2H),7.41(d,J=8.6Hz,1H),7.53(d,J=8.6Hz,2H),7.59(dd,J=8.6,2.0Hz,1H),7.63(d,J=2.0Hz,1H)IR(CHCl3)3595,3506,1614,1523,1489,1326,1281,1258,1122,1079,1057cm-1 |
I-427 | m.p.180-182℃1HNMR(CDCl3)δ1.75(s,3H),1.80(s,3H),3.44(s,3H),3.76(s,3H),4.66(d,J=6.9Hz,2H),4.87(s,1H),5.52(t,J=6.6Hz,1H),6.02(s,1H),6.46(s,1H),6.93(d,J=8.9Hz,2H),7.06(d,J=8.4Hz,1H),7.53(d,J=8.9Hz,2H),7.59(dd,J=8.4,2.1Hz,1H),7.71(d,J=2.1Hz,1H),IR(KBr)3406,1615,1522,1488,1399,1324,1280,1256,1138,1116,1076,1054,996,835,826cm-1 |
I-428 | m.p.133-135℃1HNMR(CDCl3)δ3.44(s,3H),3.75(s,3H),4.87(s,1H),5.23(s,2H),6.03(s,1H),6.46(s,1H),6.93(d,J=8.6Hz,2H),7.11(d,J=8.4Hz,1H),7.32-7.49(m,5H),7.53(d,J=8.6Hz,2H),7.60(dd,J=8.4,2.1Hz,1H),7.75(d,J=2.1Hz,1H),IR(KBr)3397,1612,1523,1489,1400,1321,1257,1132,1084,1056,1002,832cm-1 |
I-429 | m.p.174-176℃1HNMR(CDCl3)δ2.37(s,3H),3.44(s,3H),3.75(s,3H),4.88(s,1H),5.18(s,2H),6.02(s,1H),6.45(s,1H),6.93(d,J=8.6Hz,2H),7.11(d,J=8.4Hz,1H),7.21(d,J=8.1Hz,2H),7.36(d,J=8.1Hz,2H),7.53(d,J=8.6Hz,2H),7.59(dd,J=8.4,2.1Hz,1H),7.74(d,J=2.1Hz,1H),IR(KBr)3481,3376,1616,1520,1491,1327,1260,1119,1081,1004,827cm-1 |
I-430 | 1HNMR(CDCl3)δ2.37(s,3H),2.54(s,3H),2.68(s,3H),3.12(s,3H),3.54(s,3H),3.77(s,3H),5.14(s,2H),6.85(s,1H),7.12-7.24(m,3H),7.30-7.44(m,6H),7.53-7.59(m,2H)IR(CHCl3)1608,1517,1476,1367,1117,1080,1013,970,876cm-1 |
I-431 | m.p.164-168℃1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.54(s,3H),3.47(s,3H),3.75(s,3H),4.62(d,J=6.9Hz,2H),5.53(m,1H),5.69(s,1H),5.89(s,1H),6.46(s,1H),6.92-7.08(m,3H),7.30-7.38(m,2H),7.55-7.62(m,2H)IR(CHCl3)3518,2968,1584,1516,1483,1460,1414,1388,1310,1289,1243,1114,1069,1011,936,818cm-1 |
I-432 | m.p.179-181℃1HNMR(CDCl3)δ2.39(s,3H),2.54(s,3H),3.46(s,3H),3.74(s,3H),5.10(s,2H),5.67(s,1H),5.89(s,1H),6.46(s,1H),6.81(dd,J=2.1,8.4Hz,1H),7.03(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.20-7.26(m,2H),7.31-7.37(m,4H),7.55-7.61(m,2H)IR(CHCl3)3524,2930,1585,1517,1483,1460,1414,1389,1310,1289,1245,1114,1090,1070,1009,937,818cm-1 |
I-433 | m.p.111-112℃1HNMR(CDCl3)δ1.76(d,J=0.6Hz,3H),1.81(d,J=0.9Hz,3H),2.69(s,3H),3.52(s,3H),3.78(s,3H),4.63(t,J=6.6Hz,2H),5.53(m,1H),6.84(s,1H),7.02-7.25(m,5H),7.56-7.65(m,2H)IR(CHCl3)2932,1607,1520,1481,1368,1266,1080,1012,961,907,836,812cm-1 |
I-434 | m.p.97-101℃1HNMR(CDCl3)δ1.69(s,3H),1.75(d,J=0.9Hz,3H),2.48-2.58(m,5H),3.46(s,3H),3.47(s,3H),4.06(t,J=6.9Hz,2H),5.22(m,1H),5.67(s,1H),5.88(s,1H),6.46(s,1H),6.92-6.97(m,2H),7.05(m,1H),7.30-7.38(m,2H),7.55-7.62(m,2H)IR(CHCl3)3518,2928,1584,1517,1483,1414,1388,1290,1246,1114,1090,1070,1011,937,907,818cm-1 |
I-435 | m.p.127-129℃1HNMR(CDCl3)δ1.68(s,3H),1.74(d,J=1.2Hz,3H),2.50-2.60(m,2H),2.71(s,3H),3.52(s,3H),3.77(s,3H),4.04(t,J=7.2Hz,2H),5.23(m,1H),6.83(s,1H),7.00-7.21(m,5H),7.57-7.64(m,2H)IR(CHCl3)2930,1607,1520,1481,1368,1266,1080,1012,960,836,812cm-1 |
I-436 | m.p.159-161℃1HNMR(CDCl3)δ2.36(s,3H),2.57(s,3H),3.52(s,3H),3.77(s,3H),5.16(s,2H),6.83(s,1H),7.05-7.24(m,7H),7.31-7.37(m,2H),7.56-7.65(m,2H)IR(CHCl3)1520,1481,1368,1267,1131,1080,1012,960,836cm-1 |
I-437 | m.p.120-124℃1HNMR(CDCl3)δ1.76(d,J=0.6Hz,3H),1.81(d,J=0.6Hz,3H),3.43(s,3H),3.67(s,3H),4.63(d,J=6.6Hz,2H),5.56(m,1H),5.96(s,1H),6.44(s,1H),7.00-7.24(m,5H),7.57-7.66(m,2H)IR(CHCl3)3522,2930,1586,1518,1484,1415,1390,1311,1290,1248,1115,1090,1071,1012,938,818cm-1 |
I-438 | m.p.140.5-141.5℃1HNMR(CDCl3)δ2.37(s,3H),3.43(s,3H),3.75(s,3H),5.14(s,2H),5.97(s,1H),6.44(s,1H),7.04-7.28(m,7H),7.36(d,J=8.1Hz,1H),7.57-7.65(m,2H)IR(CHCl3)3496,2932,1613,1520,1488,1460,1391,1313,1267,1113,1069,1010,934,825cm-1 |
I-439 | m.p.76.5-77.5℃1HNMR(CDCl3)δ1.68(s,3H),1.74(d,J=0.9Hz,3H),2.49-2.60(m,2H),3.43(s,3H),3.75(s,3H),4.05(t,J=7.2Hz,2H),5.23(m,1H),5.96(s,1H),6.44(s,1H),6.99-7.28(m,5H),7.57-7.66(m,2H)IR(CHCl3)3498,2930,1613,1521,1489,1391,1310,1267,1113,1070,1011,934,825cm-1 |
I-440 | m.p.174-176℃1HNMR(CDCl3)δ2.80(s,3H),3.46(s,3H),3.76(s,3H),5.16(s,2H),5.71(s,1H),5.88(s,1H),6.47(s,1H),6.95(dd,J=1.8,8.4Hz,1H),7.04(d,J=8.4Hz,1H),7.08(d,J=1.8Hz,1H),7.34-7.49(m,5H),7.72-7.85(m,4H)IR(CHCl3)3518,1587,1516,1483,1459,1415,1387,1290,1114,1070,1041,1011,936,821cm-1 |
I-441 | m.p.199-202℃1HNMR(d6-DMSO)δ3.28(s,3H),3.34(s,3H),3.67(s,3H),5.14(s,2H),6.52(s,1H),6.66(dd,J=2.1,8.4Hz,1H),6.79(d,J=2.1Hz,1H),6.97(d,J=8.4Hz,1H),7.30-7.56(m,5H),7.86-7.93(m,2H),7.98-8.04(m,2H),8.65-9.02(brs,2H)IR(KBr)3487,3413,3004,1597,1518,1500,1482,1456,1360,1310,1281,1231,1146,1118,1090,1068,1016,1004,961cm-1 |
I-442 | m.p.80-84℃1HNMR(CDCl3)δ1.15(t,J=7.2Hz,3H),3.60(q,J=7.2Hz,2H),3.75(s,3H),5.03(s,1H),5.15(s,2H),5.69(s,1H),5.98(s,1H),6.45(s,1H),6.88-6.94(m,2H),6.96(dd,J=2.1,8.1Hz,1H),7.02(d,J=8.1Hz,1H),7.10(d,J=2.1Hz,1H),7.34-7.49(m,5H),7.51-7.59(m,2H)IR(CHCl3)3528,1612,1521,1488,1454,1412,1383,1286,1246,1113,1069,1023,886,825cm-1 |
I-443 | m.p.168-169℃1HNMR(CDCl3)δ1.14(t,J=6.9Hz,3H),2.66(s,3H),3.13(s,3H),3.20(s,3H),3.72(q,J=6.9Hz,2H),3.78(s,3H),5.19(s,2H),6.84(s,1H),7.15(d,J=8.4Hz,1H),7.31-7.49(m,9H),7.66-7.73(m,5H)IR(CHCl3)1517,1479,1369,1148,1117,1082,969,873cm-1 |
I-444 | m.p.192-194℃1HNMR(CDCl3)δ3.13(s,3H),3.44(s,3H),3.63(s,3H),3.76(s,3H),5.14(br,1H),5.19(s,2H),6.81-6.84(m,2H),6.94(s,1H),7.14(d,J=8.4Hz,1H),7.22-7.25(m,2H),7.37-7.50(m,5H),7.57(dd,J=8.7,2.1Hz,1H),7.67(d,J=2.1Hz,1H)IR(CHCl3)3595,3441,1730,1613,1522,1472,1371,1291,1258,1172,1164,1003,972,961,904,838cm-1 |
I-445 | m.p.179-180℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.31(s,3H),3.24(s,3H),3.45(s,3H),3.58(s,3H),3.76(s,3H),4.64(d,J=6.9Hz,2H),6.95(s,1H),7.06-7.13(m,3H),7.35-7.38(m,2H),7.57(dd,J=8.4,2.4Hz,1H),7.64(d,J=2.4Hz,1H)IR(CHCl3)2938,1732,1614,1599,1518,1470,1445,1370,1345,1290,1228,1200,1169,1116,1081,1003,973,905,846,829cm-1 |
I-446 | m.p.137-138℃1HNMR(CDCl3)δ3.13(s,3H),3.45(s,3H),3.59(s,3H),3.77(s,3H),3.88(s,3H),4.23(s,2H),5.19(s,2H),6.96(s,1H),7.15(d,J=8.7Hz,1H),7.35-7.50(m,9H),7.60(dd,J=8.7,2.4Hz,1H),7.67(d,J=2.4Hz,1H)IR(CHCl3)2954,1750,1734,1614,1516,1471,1387,1372,1345,1291,1258,1173,1147,1118,1081,1064,1004,877cm-1 |
I-447 | m.p.184-185℃1HNMR(CDCl3)δ3.44(s,3H),3.60(s,3H),3.74(s,3H),4.70(br,2H),5.17(s,2H),6.95-7.02(m,4H),7.17(dd,J=8.4,2.1Hz,1H),7.25(s,1H),7.31-7.34(d,J=8.7Hz,2H),7.38-7.47(m,5H)IR(CHCl3)3541,2937,1776,1733,1608,1519,1474,1442,1344,1291,1157,1130,1085,1063,1002,900,862,835cm-1 |
I-448 | m.p.176-178℃1HNMR(CDCl3)δ3.12(s,3H),3.44(s,3H),360(s,3H),3.76(s,3H),3.83(s,3H),4.66(s,2H),5.19(s,2H),6.91-6.96(m,3H),7.14(d,J=8.4Hz,1H),7.28-7.49(m,7H),7.57(dd,J=8.7,2.4Hz,1H),7.67(d,J=2.4Hz,1H)IR(CHCl3)2953,2939,1758,1732,1610,1519,1471,1444,1371,1345,1291,1177,1117,1085,1064,1002,973,961,904,837cm-1 |
I-449 | m.p.124-126℃1HNMR(CDCl3)δ1.69(s,3H),1.74(d,J=0.9Hz,3H),2.31(s,3H),2.53-2.60(m,2H),3.23(s,3H),3.44(s,3H),3.58(s,3H),3.76(s,3H),4.09(t,J=6.6Hz,2H),5.22(m,1H),6.95(s,1H),7.07(d,J=8.4Hz,1H),7.10-7.13(m,2H),7.34-7.37(m,2H),7.57(dd,J=9.0,2.4Hz,1H),7.64(d,J=2.4Hz,1H)IR(CHCl3)2938,1732,1614,1518,1469,1445,1370,1291,1257,1170,1167,1081,1004,973,961,906,846cm-1 |
I-450 | m.p.160-161℃1HNMR(CDCl3)δ1.69(s,3H),1.74(d,J=0.9,3H),2.53-2.60(m,2H),3.23(s,3H),3.44(s,3H),3.62(s,3H),3.76(s,3H),4.08(d,J=6.6Hz,2H),4.91(br,1H),5.20-5.25(m,1H),6.83-6.86(m,2H),6.94(s,1H),7.06(d,J=8.7Hz,2H),7.23-7.26(m,2H),7.57(dd,J=8.7,2.4Hz,1H),7.64(d,J=2.4Hz,1H)IR(CHCl3)3595,3448,2937,1730,1613,1522,1469,1445,1370,1345,1292,1260,1172,1117,1081,1064,1003,973,864,837cm-1 |
1-451 | m.p.182-184℃1HNMR(CDCl3)δ1.70(d,J=0.6Hz,3H),1.81(d,J=0.9Hz,3H),3.24(s,3H),3.45(s,3H),3.63(s,3H),3.75(s,3H),4.64(d,J=6.6Hz,2H),5.48-5.54(m,1H),5.76(br,1H),6.78-6.82(m,2H),6.95(s,1H),7.08(d,J=8.7Hz,1H),7.19-7.24(m,2H),7.56(dd,J=8.7,2.4Hz,1H),7.64(d,J=2.4Hz,1H)IR(CHCl3)3595,3445,2939,1730,1613,1522,1471,1445,1369,1345,1291,1257,1172,1116,1081,1064,1002,973,904,838cm-1 |
I-452 | m.p.250-253℃(dec.)1HNMR(CD3OD)δ3.41(s,3H),3.71(s,3H),4.58(s,2H),5.21(s,2H),6.29-6.95(m,3H),7.02-7.03(m,2H),7.17(s,1H),7.26 7.41(m,5H),7.49-7.52(m,2H)IR(KBr)3424,2933,2553,1709,1608,1519,1467,1383,1333,1291,1229,1129,1084,1060,1001,916,861,841,727,697cm-1 |
I-453 | 泡沫1HNMR(CDCl3)δ1.69(s,3H),1.75(d,J=1.2Hz,3H),2.51-2.58(m,2H),3.43(s,3H),3.62(s,3H),3.75(s,3H),4.08(t,J=6.9Hz,2H),4.85(br,1H),5.23(m,1H),5.71(br,1H),6.82-6.85(m,2H),6.90-6.94(m,2H),7.16(dd,J=8.4,2.1Hz,1H),7.23-7.26(m,3H)IR(CHCl3)3596,3541,2936,1730,1612,1590,1522,1470,1395,1345,1290,1258,1173,1130,1081,1063,1004,861,836cm-1 |
I-454 | m.p.166-167℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.48(s,3H),3.75(s,3H),4.64(d,J=6.6Hz,2H),5.51-5.55(m,1H),5.75(br,1H),6.77-6.80(m,2H),6.93-6.96(m,2H),7.17(dd,J=8.1,2.1Hz,1H),7.23-7.28(m,3H)IR(KBr)3447,2937,1590,1559,1522,1473,1382,1338,1295,1259,1131,1080,1059,999,918,862,837,815,791,754cm-1 |
I-455 | m.p.168-170℃1HNMR(CD3OD)δ1.68(s,3H),1.74(s,3H),2.50-2.58(m,2H),3.41(s,3H),3.73(s,3H),4.05(t,J=6.9Hz,2H),5.29(m,1H),6.76-6.79(m,2H),6.98-7.17(m,6H)IR(KBr)3411,2964,2936,1685,1613,1590,1523,1472,1379,1293,1259,1229,1131,1082,1061,1000,962,861,838,814,791,754,529cm-1 |
I-456 | m.p.153-155℃1HNMR(CDCl3)δ3.14(s,3H),3.50(s,3H),3.77(s,3H),5.20(s,2H),7.10-7.28(m,6H),7.38-7.50(m,5H),7.56(dd,J=8.4,2.1Hz,1H),7.65(d,J=2.1Hz,1H),9.98(s,1H)IR(CHCl3)2938,2843,1697,1604,1590,1517,1469,1372,1331,1293,1254,1172,1159,1123,1093,1005,963,818cm-1 |
I-457 | m.p.143-145℃1HNMR(CDC13)δ1.77(s,3H),1.83(s,3H),3.44(s,3H),3.63(s,3H),3.75(s,3H),4.63(d,J=6.6Hz,2H),5.53(m,1H),5.72(br,1H),6.82-6.85(m,2H),6.92-6.95(m,2H),7.16(dd,J=8.4,2.4Hz,1H),7.23-7.26(m,3H)IR(CHCl3)3595,3537,2938,1729,1612,1591,1522,1473,1395,1344,1290,1258,1173,1129,1081,1063,1003,900,862,836cm-1 |
I-458 | 粉末1HNMR(CDCl3)δ2.37(s,3H),3.08(s,3H),3.11(s,3H),3.21(s,3H),3.51(s,3H),3.52(s,3H),5.26(s,2H),7.19-7.23(m,2H),7.36-7.43(m,4H),7.45-7.50(m,2H),7.82(d,J=2.1Hz,1H),7.98(d,J=2.1Hz,1H)IR(CHCl3)3033,2942,1543,1377,1220,1181,1153,1034cm-1 |
I-459 | m.p.182-187℃(dec.)1HNMR(CDCl3)δ2.36(s,3H),2.73(s,3H),3.16(s,3H),3.22(s,3H),3.43(s,3H),3.47(s,3H),5.08(s,2H),6.85(brs,1H),6.92(brs,1H),7.17-7.21(m,2H),7.32-7.38(m,2H),7.39-7.44(m,2H),7.50-7.55(m,2H)IR(CHCl3)3030,2939,1618,1599,1513,1468,1416,1372,1178,1150,1031cm-1 |
I-460 | 粉末1HNMR(CDCl3)δ2.38(s,3H),2.83(s,3H),3.05(s,3H),3.22(s,3H),3.56(s,3H),3.80(s,3H),3.91(s,3H),5.13(s,2H),6.86(s,1H),7.20-7.24(m,2H),7.37-7.46(m,4H),7.65-7.70(m,3H),7.89(d,J=2.1Hz,1H)IR(CHCl3)3032,2940,1728,1473,1373,1232,1179,1150,1085cm-1 |
I-461 | 无定形1HNMR(CDCl3)δ3.78(s,6H),5.16(s,2H),5.31(d,J=3.6Hz,1H),5.72(s,1H),6.91(s,1H),6.94(s,1H),6.99(d,J=8.2Hz,1H),7.04(t,J=8.6Hz,1H),7.08(dd,J=8.2,2.1Hz,1H),7.22(d,J=2.1Hz,1H),7.25(ddd,J=8.6,1.8,0.9Hz,1H),7.34-7.46(m,6H)IR(CHCl3)3577,3548,1526,1495,1280,1635cm-1 |
I-462 | m.p.153-155℃1HNMR(CDCl3)δ3.12(s,3H),3.26(s,3H),3.80(s,3H),3.81(s,3H),5.18(s,2H),6.91(s,1H),6.94(s,1H),7.12(d,J=8.4Hz,1H),7.36-7.50(m,8H),7.59(d,J=1.8Hz,1H)IR(CHCl3)1494,1367,1212,1180,1116,872,808cm-1 |
I-463 | m.p.125-127℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.23(s,3H),3.27(s,3H),3.80(s,3H),3.82(s,3H),4.64(d,J=6.7Hz,2H),5.51(t,J=6.7Hz,1H),6.91(s,1H),6.95(s,1H),7.06(d,J=8.7Hz,1H),7.37(dd,J=8.7,1.9Hz,1H),7.40-7.47(m,2H),7.50(d,J=2.4Hz,1H),7.57(d,J=1.9Hz,1H)IR(KBr)1523,1496,1370,1213,1175,1116,1035,977,832,807cm-1 |
I-464 | m.p.149-151℃1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.55(q,J=7.0Hz,2H),3.21(s,3H),3.26(s,3H),3.80(s,3H),3.81(s,3H),4.07(t,J=7.0Hz,2H),5.21(t,J=7.0Hz,1H),6.91(s,1H),6.94(s,1H),7.05(d,J=8.4Hz,1H),7.37(dd,J=8.4,2.1Hz,1H),7.40-7.47(m,2H),7.50(d,J=2.1Hz,1H),7.57(d,J=2.1Hz,1H)IR(KBr)1523,1495,1368,1212,1176,1116,1035,976,832,806cm-1 |
I-465 | m.p.148-150℃1HNMR(CDCl3)δ2.38(s,3H),3.11(s,3H),3.26(s,3H),3.80(s,3H),3.81(s,3H),5.13(s,2H),6.91(s,1H),6.94(s,1H),7.12(d,J=8.4Hz,1H),7.22(d,J=7.8Hz,2H),7.35(d,J=7.8Hz,2H),7.37(dd,J=8.4,1.8Hz,1H),7.40-7.50(m,3H),7.59(d,J=1.8Hz,1H)IR(KBr)1523,1490,1370,1181,1115,971,868,806cm-1 |
I-466 | m.p.109-112℃1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.79(s,6H),4.62(d,J=6.9Hz,2H),5.26(d,J=3.9Hz,1H),5.52(t,J=6.9Hz,1H),5.72(s,1H),6.91(s,1H),6.93(d,J=8.6Hz,1H),6.94(s,1H),7.04(t,J=8.7Hz,1H),7.07(dd,J=8.6,2.1Hz,1H),7.19(d,J=2.1Hz,1H),7.25(ddd,J=8.7,1.8,0.9Hz,1H),7.37(dd,J=12.0,1.8Hz,1H)IR(CHCl3)3578,3542,1526,1495,1280,1055,1035cm-1 |
I-467 | 无定形1HNMR(CDCl3)δ2.39(s,3H),3.79(s,6H),5.11(s,2H),5.40(brs,1H),5.73(s,1H),6.91(s,1H),6.94(s,1H),6.99(d,J=8.4Hz,1H),7.04(t,J=8.7Hz,1H),7.08(dd,J=8.4,2.1Hz,1H),7.21(d,J=2.1Hz,1H),7.23(d,J=7.7Hz,2H),7.25(ddd,J=8.7,2.1,1.2Hz,1H),7.34(d,J=7.7Hz,2H),7.37(dd,J=11.7,2.1Hz,1H)IR(CHCl3)3577,3545,1526,1495,1280,1055,1035,868cm-1 |
I-468 | 无定形1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.53(q,J=7.0Hz,2H),3.78(s,3H),3.79(s,3H),4.07(t,J=7.2Hz,2H),5.22(t,J=7.0Hz,1H),5.27(d,=3.9Hz,1H),5.71(s,1H),6.91(s,1H),6.91(d,J=8.6Hz,1H),6.94(s,1H),7.04(t,J=8.4Hz,1H),7.06(dd,J=8.6,2.1Hz,1H),7.19(d,J=2.1Hz,1H),7.25(ddd,J=8.4,1.9,1.1Hz,1H),7.37(dd,J=12.0,1.9Hz,1H)IR(CHCl3)3578,1526,1495,1280,1055,1035cm-1 |
I-469 | m.p.190-191℃1HNMR(CDCl3)δ2.38(s,3H),3.11(s,3H),3.19(s,3H),3.80(s,6H),5.13(s,2H),6.92(s,1H),6.94(s,1H),7.12(d,J=8.7Hz,1H),7.22(d,J=7.8Hz,1H),7.32-7.37(m,4H),7.49(dd,J=2.1,8.4Hz,1H),7.59(d,J=1.8Hz,1H),7.60-7.65(m,2H)IR(KBr)3600-2800(br),1521,1492,1468,1386,1366,1336,1292,1272,1259,1202,1174,1150,1113cm-1 |
I-470 | m.p.147-148℃1HNMR(CDCl3)δ2.37(s,3H),3.19(s,3H),3.79(s,3H),3.80(s,3H),5.16(s,2H),6.92(s,1H),6.93(s,1H),7.06(t,J=8.7Hz,1H),7.20-7.27(m,3H),7.32-7.41(m,5H),7.60-7.64(m,2H)IR(KBr)3600-2800(br),1523,1492,1462,1454,1379,1359,1299,1278,1264,1210,1175,1151,1129,1054,1031,1009cm-1 |
I-471 | m.p.170-172℃1HNMR(CDCl3)δ3.19(s,3H),3.24(s,3H),3.79(s,3H),3.80(s,3H),5.12(s,2H),6.92(s,1H),6.94(s,1H),7.11(d,J=8.7Hz,1H),7.26-7.30(m,2H),7.32-7.37(m,2H),7.47(dd,J=2.4,8.4Hz,1H),7.61-7.64(m,3H),7.74-7.80(m,1H),8.61-8.63(m,1H)IR(KBr)3600-2800(br),1522,1491,1462,1361,1296,1264,1212,1177,1149,1115,1030cm-1 |
I-472 | m.p.174-175℃1HNMR(CDCl3)δ3.19(s,3H),3.79(s,3H),3.80(s,3H),5.33(s,2H),6.92(s,1H),6.93(s,1H),7.07(d,J=8.7Hz,1H),7.23-7.28(m,2H),7.32-7.37(m,2H),7.41(dd,J=1.8,12.6Hz,1H),7.60-7.64(m,3H),7.73-7.79(m,1H),8.60-8.63(m,1H)IR(KBr)3600-2800(br),1524,1491,1464,1380,1361,1302,1267,1209,1172,1149,1130,1034,1024,1008cm-1 |
I-473 | m.p.118.5-119.5℃1HNMR(CDCl3)δ1.77(s,3H),1.80(d,J=0.9Hz,3H),3.78(s,3H),3.79(s,3H),4.63(d,J=6.9Hz,2H),5.52-5.57(m,1H),6.73-6.78(m,2H),6.91(s,1H),6.93(s,1H),7.02(t,J=8.7Hz,1H),7.25-7.30(m,1H),7.35-7.43(m,3H)IR(KBr)3600-2800(br),1625,1527,1491,1461,1449,1378,1298,1279,1259,1207,1184,1125,1055,1031cm-1 |
I-474 | m.p.156-158℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.08(s,3H),3.80(s,3H),3.81(s,3H),4.64(d,J=6.6Hz,2H),5.52-5.58(m,1H),6.43(brs,1H),6.93(s,1H),6.94(s,1H),7.03(t,J=8.4Hz,1H),7.26-7.30(m,3H),7.37(dd,J=1.8,12.6Hz,1H),7.57-7.61(m,2H)IR(KBr)3600-2800(br),1526,1495,1463,1382,1325,1300,1267,1210,1156,1139,1129,1054,1032cm-1 |
I-475 | m.p.158-160℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.80(s,6H),4.64(d,J=6.6Hz,2H),4.73(brs,2H),5.53-5.57(m,1H),6.51(brs,1H),6.93(s,1H),6.94(s,1H),7.03(t,J=8.7Hz,1H),7.26-7.31(m,3H),7.37(dd,J=2.1,12.6Hz,1H),7.57-7.61(m,2H)IR(KBr)3600-2800(br),1527,1495,1462,1395,1326,1299,1264,1208,1170,1130,1054,1031cm-1 |
I-476 | m.p.138-140℃1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.21(s,3H),3.78(s,3H),3.80(s,3H),4.63(d,J=6.9Hz,2H),5.53-5.57(m,1H),6.93(s,1H),6.94(s,1H),7.03(t,J=8.4Hz,1H),7.20(brs,1H),7.26-7.30(m,1H),7.37(dd,J=2.1,12.6Hz,1H),7.56(m,4H)IR(KBr)3600-2800(br),1666,1604,1527,1494,1463,1448,1379,1317,1299,1264,1209,1130,1055,1032cm-1 |
I-477 | m.p.200-202℃1HNMR(CDCl3+CD3OD)δ1.77(s,3H),1.81(s,3H),3.79(s,3H),3.80(s,3H),4.64(d,J=6.6Hz,2H),5.52-5.57(m,1H),6.93(s,1H),6.94(s,1H),7.03(t,J=9.0Hz,1H),7.27-7.30(m,1H),7.34-7.41(m,3H),7.52-7.55(m,2H)IR(KBr)3600-2800(br),2404,1684,1660,1584,1528,1493,1462,1386,1301,1274,1263,1209,1132,1053,1029cm-1 |
I-478 | m.p.195-196.5℃1HNMR(CDCl3)δ1.55(s,9H),3.78(s,3H),3.79(s,3H),4.85(s,1H),6.75(brs,1H),6.88-6.92(m,2H),6.92(s,1H),6.93(s,1H),7.31-7.39(m,3H),7.45-7.49(m,2H),8.12(t,J=7.5Hz,1H)IR(KBr)3600-2800(br),1729,1590,1531,1500,1464,1394,1261,1240,1199,1156,1055,1033,1023cm-1 |
I-479 | m.p.172-174℃1HNMR(CDCl3)δ1.55(s,9H),3.19(s,3H),3.79(s,3H),3.80(s,3H),6.75(d,J=2.1Hz,1H),6.92(s,1H),6.94(s,1H),7.26-7.39(m,5H),7.60-7.65(m,2H)IR(KBr)3600-2800(br),1728,1590,1531,1513,1494,1464,1391,1367,1352,1240,1206,1179,1145,1056,1033,1024cm-1 |
I-480 | m.p.152-153℃1HNMR(CDCl3)δ1.74(s,3H),1.77(s,3H),3.18(s,3H),3.78(d,J=9.9Hz,2H),3.79(s,6H),3.93(brs,1H),5.35-5.40(m,1H),6.75(t,J=8.4Hz,1H),6.91(s,1H),6.95(s,1H),7.24-7.36(m,4H),7.60-7.65(m,2H)IR(KBr)3600-2800(br),1630,1530,1488,1466,1380,1366,1346,1259,1213,1176,1149,1124,1054,1027cm-1 |
I-481 | 泡沫1HNMR(CDCl3)δ2.40(s,3H),3.19(s,3H),3.77(s,3H),3.78(s,3H),6.80(t,d=2.4Hz,1H),6.90(s,1H),6.91(s,1H),7.25-7.36(m,6H),7.58-7.65(m,3H),7.72-7.76(m,2H)IR(KBr)3600-2800(br),1522,1490,1366,1342,1211,1164,1151,1091,1053,1030cm-1 |
I-482 | m.p.201-203℃1HNMR(CDCl3)δ2.45(s,3H),3.20(s,3H),3.82(s,6H),6.95(s,1H),6.98(s,1H),7.32-7.48(m,6H),7.61-7.66(m,2H),7.80-7.84(m,2H),8.10(d,J=3.3Hz,1H),8.55(d,J=8.4Hz,1H)IR(KBr)3600-2800(br),1671,1592,1524,1494,1388,1366,1328,1265,1207,1172,1150,1052,1024cm-1 |
I-483 | m.p.132-134℃1HNMR(CDCl3)δ1.55(s,9H),3.00(s,6H),3.79(s,6H),6.73(d,J=2.4Hz,1H),6.81(m,2H),6.92(s,1H),6.96(s,1H),7.32-7.39(m,2H),7.48-7.52(m,2H),8.11(t,J=8.1Hz,1H)IR(KBr)3600-2800(br),1728,1610,1591,1533,1499,1459,1446,1381,1365,1238,1206,1159,1055,1030cm-1 |
I-484 | 泡沫1HNMR(CDCl3)δ1.74(s,3H),1.77(s,3H),3.00(s,6H),3.78(d,J=9.6Hz,1H),3.78(s,3H),3.79(s,3H),5.34-5.38(m,1H),6.75(t,J=8.4Hz,1H),6.92(s,1H),6.94(s,1H),6.93-6.95(m,1H),7.23-7.32(m,3H),7.48-7.52(m,2H)IR(KBr)3600-2800(br),1625,1611,1531,1494,1446,1380,1340,1257,1207,1123,1055,1032cm-1 |
I-485 | 泡沫1HNMR(CDCl3)δ2.40(s,3H),3.00(s,6H),3.76(s,3H),3.77(s,3H),6.70(t,J=2.4Hz,1H),6.80(t,J=8.7Hz,2H),6.87(s,1H),6.94(s,1H),7.24-7.33(m,4H),7.46-7.50(m,2H),7.60(t,J=9.0Hz,1H),7.71-7.75(m,2H)IR(KBr)3600-2800(br),1609,1529,1493,1446,1381,1340,1208,1164,1090,1054,1031cm-1 |
I-486 | m.p.184-186℃1HNMR(CDCl3)δ2.45(s,3H),3.01(s,6H),3.80(s,3H),3.81(s,3H),6.82(d,J=7.5Hz,2H),6.95(s,1H),6.98(s,1H),7.32(d,J=8.1Hz,2H),7.40-7.52(m,4H),7.80-7.84(m,2H),8.08(d,J=2.7Hz,1H),8.52(t,J=8.4Hz,1H)IR(KBr)3600-2800(br),1647,1608,1530,1497,1379,1365,1284,1267,1206,1051,1030cm-1 |
I-487 | 泡沫1HNMR(CDCl3)δ2.36(s,3H),3.77(s,6H),4.81(brs,1H),6.69(dd,J=0.9,3.6Hz,1H),6.88-6.92(m,2H),6.94(s,1H),6.95(s,1H),7.23-7.26(m,2H),7.46-7.51(m,2H),7.53(dd,J=1.5,8.4Hz,1H),7.59(d,J=3.6Hz,1H),7.73(d,J=0.9Hz,1H),7.80-7.84(m,2H),8.02(d,J=8.4Hz,1H)IR(KBr)3600-2800(br),1611,1594,1520,1498,1459,1444,1369,1259,1208,1170,1129,1092,1051,1028cm-1 |
I-488 | m.p.219-220℃1HNMR(CDCl3)δ2.37(s,3H),3.19(s,3H),3.78(s,3H),3.79(s,3H),6.70(dd,J=0.9,3.6Hz,1H),6.94(s,1H),6.97(s,1H),7.24-7.27(m,2H),7.32-7.37(m,2H),7.53(dd,J=1.8,8.7Hz,1H),7.60(d,J=3.6Hz,1H),7.61-7.66(m,2H),7.73(d,J=0.9Hz,1H),7.80-7.84(m,2H),8.03(d,J=8.7Hz,1H)IR(KBr)3600-2800(br),1513,1494,1464,1444,1373,1209,1173,1155,1122,1049cm-1 |
I-489 | 1HNMR(CDCl3)δ3.79(s,3H),3.80(s,3H),3.94(s,3H),5.17(s,2H),5.71(s,1H),6.96(s,1H),6.97(s,1H),6.99(d,J=8.7Hz,1H),7.09(d.d,J=8.7&2.4Hz,1H),7.22(d,J=2.4Hz),7.26(s,1H),7.32-7.49(m,5H),7.66(d,J=8.7Hz,2H),8.09(d,J=8.7Hz,2H)IR(KBr)3383,1702,1606,1489,1381,1291,1206,1111,1032,1002cm-1 |
I-490 | 1HNMR(CDCl3)δ3.12(s,3H),3.79(s,3H),3.81(s,3H),395(s,3H),5.18(s,2H),6.96(s,2H),7.12(d,J=8.4Hz,1H),7.31-7.53(m,6H),7.60(d,J=2.1Hz,1H),7.65(d,J=8.7Hz,2H),8.10(d,J=8.7Hz,2H)IR(KBr)1720,1607,1492,1362,1275,1211,1112,1057,1032cm-1 |
I-491 | 1HNMR(CDCl3)δ3.12(s,3H),3.80(s,3H),3.81(s,3H),5.18(s,2H),6.92(s,1H),6.96(s,1H),7.13(d,J=8.4Hz,1H),7.31-7.52(m,6H),7.70(d,J=2.1Hz,1H),7.66-7.77(m,4H)IR(KBr)3433,1685,1606,1509,1492,1372,1318,1264,1211,1183,1111,1055,1031cm-1 |
I-492 | 1HNMR(CDCl3)δ3.79(s,3H),3.80(s,3H),5.17(s,2H),5.71(s,2H),6.91(s,1H),6.97(s,1H),7.00(d,J=8.4Hz,1H),7.08(dd,J=8.4&2.4Hz,1H),7.22(d,J=2.4Hz,1H),7.32-7.49(m,5H),7.70(s,4H)IR(KBr)3291,2242,1607,1579,1488,1384,1324,1272,1209,1130,1054,1034,1001cm-1 |
I-493 | 1HNMR(CDCl3)δ3.12(s,3H),3.80(s,3H),3.81(s,3H),5.18(s,2H),6.92(s,1H),6.96(s,1H),7.12(d,J=8.4Hz,1H),7.31-7.72(m,6H),7.60(d,J=1.8Hz,1H),7.65-7.74(m,4H)IR(KBr)2223,1604,1490,1363,1296,1264,1213,1172,1117,1055,1036,1026cm-1 |
I-494 | 1HNMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.23(s,3H),3.80(s,3H),3.81(s,3H),3.95(s,3H),4.64(d,J=6.6Hz,2H),5.51(t,J=6.6Hz,1H),6.96(s,2H),7.06(d,J=8.7Hz,1H),7.50(d.d,J=8.7&2.1Hz,1H),7.59(d,J=2.1Hz,1H),7.65(d,J=8.7Hz,2H),8.10(d,J=8.7Hz,2H)IR(KBr)1720,1608,1508,1492,1384,1357,1273,1179,1110,1026,1019cm-1 |
I-495 | 1HNMR(CDCl3)δ2.38(s,3H),3.12(s,3H),3.80(s,6H),3.81(s,3H),3.95(s,3H),5.14(s,2H),6.96(s,2H),7.13(d,J=8.4Hz,1H),7.21(d,J=7.8Hz,2H),7.35(d,J=7.8Hz,2H),7.49(d,d,J=8.4&1.8Hz,1H),7.60(d,J=1.8Hz,1H),7.65(d,J=8.7Hz,2H),8.10(d,J=8.7Hz,2H)IR(KBr)1697,1607,1492,1364,1286,1263,1213,1178,11115,1057,1030cm-1 |
I-496 | IR(KBr)1730,1701,1610,1515,1465,1359,1238,1186,1116,1082,1064,1016cm-1 |
I-497 | 1HNMR(CDCl3)δ1.75(s,3H),1.80(s,3H),2.89(s,6H),3.21(s,3H),3.44(s,3H),3.68(s,3H),3.77(s,1H),4.61(d,J=8.4Hz,2H),5.49(t,J=8.4Hz,1H),6.92(s,1H),7.01(d,J=8.4Hz,1H),7.25-7.28(m,3H),7.33(d,J=2.1Hz,1H),7.52(dd,J=8.4&1.8Hz,1H),7.66(d,J=2.4Hz,1H)IR(KBr)1727,1598,1515,1467,1360,1295,1258,1241,1116,1084cm-1 |
I-498 | 1HNMR(CDCl3)δ2.38(s,3H),2.89(s,6H),3.10(s,3H),3.44(s,3H),3.66(s,3H),3.77(s,3H),5.11(s,3H),6.93(s,1H),7.06-7.15(m,2H),7.17-7.29(m,4H),7.31-7.37(m,3H),7.53(d.d,J=8.7&1.8Hz,1H),7.66(dJ=1.8Hz,1H)IR(KBr)1732,1701,1598,1518,1466,1352,1294,1121,1085,1060,1015cm-1 |
I-499 | 1HNMR(CDCl3)δ2.88(s,6H),3.44(s,3H),3.64(s,3H),3.77(s,3H),5.17(s,2H),5.65(s,1H),6.84(dd,J=8.1&2.1Hz,1H),6.92(s,1H),6.95(d,J=8.1Hz,1H),7.01(d,J=2.1Hz,1H),7.12(d,J=8.4Hz,1H),7.31-7.46(m,6H),7.53(d.d,J=8.4&1.8Hz,1H),7.66(d,J=1.8Hz,1H)IR(KBr)3526,3434,1732,1598,1515,1460,1344,1260,1240,1222,1061,1013cm-1 |
I-500 | 1HNMR(CDCl3)δ2.60(s,3H),3.43(s,3H),3.72(s,3H),3.75(s,3H),5.17(s,2H),5.67(s,1H),6.77(s,1H),6.94(dd,J=8.4&1.8Hz,1H),702(d,J=8.4Hz,1H),7.06(d,J=1.8Hz,1H),7.32-7.50(m,7H),7.53-7.62(m,1H),7.94(d,J=7.8Hz,1H)IR(KBr)1732,1719,1585,1521,1481,1403,1352,1289,1253,1225,1172,1073,1012cm-1 |
1-501 | 1HNMR(CDCl3)δ2.73(s,3H),3.12(s,3H),3.43(s,3H),3.72(s,3H),3.76(s,3H),5.19(s,2H),6.78(s,1H),7.15(d,J=8.4Hz,1H),7.31-7.63(m,10H),9.96(d,J=6.6Hz,1H)IR(KBr)1726,1609,1520,1480,1400,1371,1294,1262,1179,1075,1009cm-1 |
I-502 | 1HNMR(CDCl3)δ1.78(s,3H),1.81(s,3H),3.22(s,3H),3.48(s,3H),3.77(s,3H),3.77(s,3H)),3.82(s,3H),4.66(d,J=6.9Hz,2H),5.56(t,J=6.9Hz,1H),6.62(s,1H),6.70(s,1H),7.11(s,1H),7.38(d,J=8.7Hz,1H),7.69(d,J=8.7Hz,1H)IR(KBr)1699,1607,1587,1516,1468,1354,1216,1152,1067,1044,1004cm-1 |
I-503 | 1HNMR(CDCl3)δ1.78(s,3H),1.81(s,3H),3.21(s,3H),3.48(s,3H),3.72(s,3H),3.74(s,3H),3.82(s,3H),4.33(d,J=11.7Hz,1H),4.54(dJ=11.7Hz,1H),4.65(d,J=8.4Hz,1H),5.57(t,J=8.4Hz,1H),6.68(s,1H),6.69(s,1H),6.89(s,1H),7.38(d,J=8.7Hz,2H),7.73(d,J=8.7Hz,2H)IR(KBr)3530,1609,1515,1467,1356,1214,1174,1151,1075,1039,1004cm-1 |
I-504 | 1HNMR(CDCl3)δ1.77(s,3H),1.80(s,3H),3.22(s,3H),3.45(s,3H),3.75(s,3H),3.77(s,3H),3.81(s,3H),4.62(d,J=6.9Hz,2H),5.55(t,J=6.9Hz,1H),6.64(s,1H),6.77(s,1H),6.97(s,1H),7.39(d,J=8.7Hz,2H),7.72(d,J=8.7Hz,2H)IR(KBr)3431,1735,1706,1609,1514,1474,1367,1206,1176,1150,1055,1039cm-1 |
I-505 | 1HNMR(CDCl3)δ1.77(s,3H),1.80(s,3H),2.94(broad,1H),3.47(s,3H),3.72(s,3H),3.73(s,3H),3.81(s,3H),4.32(s,1H),4.36(s,1H),4.65(d,J=6.6Hz,2H),5.34(s,1H),5.57(t,J=6.6Hz,1H),6.69(s,1H),6.70(s,1H),6.89(s,1H),6.91(d,J=8.1Hz,2H),7.55(d,J=8.1Hz,2H)IR(KBr)3466,1610,1517,1475,1463,1386,1265,1215,1170,1147,1075,1042,1007cm-1 |
I-506 | 1HNMR(CDCl3)δ1.76(s,3H),1.79(s,3H),3.44(s,3H),3.74(s,3H),3.76(s,3H),3.80(s,3H),4.63(d,J=7.2Hz,2H),5.30(s,1H),5.49-5.60(m,1H),6.63(s,1H),6.78(s,1H),6.94(d,J=8.7Hz,2H),6.97(s,1H),7.54(.d,J=8.7Hz,2H)IR(KBr)3382,1726,1699,1611,1519,1470,1206,1174,1143,1074,1056,997cm-1 |
I-507 | 1HNMR(CDCl3)δ1.77(s,3H),1.79(s,3H),3.41(s,3H),3.60(s,3H),3.74(s,3H),3.77(s,3H),3.81(s,3H),4.63(d,J=6.9Hz,2H),4.74-5.02(broad,1H),5.52-5.60(m,1H),6.63(s,1H),6.75(s,1H),6.91(d,J=8.7Hz,2H),6.94(s,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3423,1734,1612,1520,1475,1441,1395,1337,1267,1215,1173,1140,1017,cm-1 |
I-508 | 1HNMR(CDCl3)δ3.21(s,3H),3.45(s,3H),3.73(s,3H),4.41-4.62(m,2H),5.16(s,2H),5.71(s,1H),6.79(d.d,J=8.1&2.1Hz,1H),6.84(s,1H),6.92(d,J=2.1Hz,1H),7.01(d,J=8.1Hz,1H),7.32-7.50(m,7H),7.71(d,J=8.4Hz,2H)IR(KBr)3496,3255,1607,1590,1528,1473,1464,1358,1247,1147,1071,1017cm-1 |
I-509 | 1HNMR(CDCl3)δ3.21(s,3H),3.45(s,3H),3.73(s,3H),3.89(s,3H),4.51(d,J=6.3Hz,2H),5.20(s,2H),6.80(d.d,J=8.1&2.1Hz,1H),6.85(s,1H),6.89(d,J=2.1Hz,1H),6.97(d,J=8.1Hz,1H),7.29-7.51(m,7H),7.71(d,J=8.7Hz,2H)IR(KBr)3412,1603,1586,1515,1464,1364,1242,1175,1151,1081,1020,1006cm-1 |
I-510 | 1HNMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.22(s,3H),3.45(s,3H),3.73(s,3H),3.87(s,3H),4.52(s,2H),4.64(d,J=6.6Hz,2H),5.57(t,J=6.6Hz,1H),6.83(dd,J=7.5&1.2Hz,1H),6.86(d,J=1.2Hz,1H),6.96(d,J=7.5Hz,1H)IR(KBr)3433,1598,1579,1517,1469,1372,1244,1221,1174,1149,1072,1017cm-1 |
I-511 | 1HNMR(CDCl3)δ2.36(s,3H),3.21(s,3H),3.45(s,3H),3.72(s,3H),3.88(s,3H),4.50(s,2H),5.16(s,2H),6.80(dd,J=8.1&2.1Hz,1H),6.85(s,1H),6.88(d,J=2.1Hz,1H),6.97(d,J=8.1Hz,1H),7.20(d,J=8.4Hz,2H),7.33-7.42(m,4H),7.71(d,J=8.4Hz,2H)IR(KBr)3502,1604,1510,1465,1383,1360,1266,1239,1227,1147,1071,1008cm-1 |
I-512 | 1HNMR(CDCl3)δ3.45(s,3H),3.72(s,3H),3.89(s,3H),4.48(s,2H),5.20(s,2H),6.81(dd,J=8.1&2.1Hz,1H),6.86(s,1H),6.88-6.99(m,4H),7.27-7.43(m,3H),7.46-7.54(m,4H)IR(KBr)3528,1610,1591,1517,1474,1461,1438,1388,1263,1239,1173,1140,1017,cm-1 |
I-513 | 1HNMR(CDCl3)δ1.75(s,3H),1.79(s,3H),2.47(broads,1H),3.45(s,3H),3.73(s,3H),3.86(s,3H),4.52(s,2H),4.63(d,J=6.6Hz,2H),5.16(s,1H),5.56(d,J=6.6Hz,1H),6.82-6.97(m,6H),7.53(d,J=9.0Hz,2H)IR(KBr)3477,3246,1609,1586,1518,1464,1439,1387,1266,1240,1221,1173,1141,1079,1011,1002cm-1 |
I-514 | 1HNMR(CDCl3)δ2.36(s,3H),2.48(broad,1H),3.44(s,3H),3.72(s,3H),3.88(s,3H),4.50(s,2H),5.16(s,3H),6.76-6.98(m,6H),7.19(d,J=7.8Hz,2H),7.36(d,J=7.8Hz,2H),7.52(d,J=8.7Hz,2H)IR(KBr)3544,3239,1614,1593,1519,1463,1386,1266,1240,1218,1173,1139,1074,1010cm-1 |
I-515 | m.p.159-160℃1HNMR(CDCl3)δ3.19(s,3H),3.34(s,3H),3.79(s,3H),3.80(s,3H),5.18(ABq,J=12.3Hz,2H),6.92(s,1H),6.93(s,1H),7.08(d,J=8.7Hz,1H),7.33-7.64(m,11H)IR(KBr)3433,2937,1694,1520,1492,1369,1288,1243,1211,1176,1150,1100cm-1 |
I-516 | 1HNMR(CDCl3)δ2.91(s,3H),3.777(s,3H),3.783(s,3H),4.85(brs,1H),5.12(s,2H),6.87-7.00(m,7H),7.32-7.50(m,7H)IR(KBr)3432,2938,1609,1590,1525,1494,1380,1254,1207,1174,1152,1058,1031cm-1 |
I-517 | m.p.213-215℃1HNMR(CDCl3)δ2.99(s,3H),3.779(s,3H),3.804(s,3H),4.86(brs,1H),5.16(s,2H),6.83(brs,1H),6.93(s,1H),6.94(s,1H),7.06(d,J=8.7Hz,1H),7.35(dd,J=2.1,8.7Hz,1H),7.41-7.49(m,7H),7.81(d,J=2.1Hz,1H)IR(KBr)3409,3374,1610,1525,1491,1371,1321,1251,1208,1145,1120,1037cm-1 |
I-518 | 粉末1HNMR(CDCl3)δ1.75(s,3H),1.81(s,3H),2.84(s,3H),3.21(s,3H),3.22(s,3H),3.55(s,3H),3.79(s,3H),3.93(s,3H),4.67(d,J=7.2Hz,2H),5.59(m,1H),6.85(s,1H),7.36-7.42(m,2H),7.62(d,J=2.1Hz,1H),7.65-7.70(m,2H),7.86(d,J=2.1Hz,1H)IR(CHCl3)3026,2940,1728,1510,1473,1373,1179,1150,1086cm-1 |
I-519 | 粉末1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.52-2.61(m,2H),2.86(s,3H),3.20(s,3H),3.21(s,3H),3.55(s,3H),3.79(s,3H),3.93(s,3H),4.21(t,J=6.9Hz,2H),5.26(m,1H),6.86(s,1H),7.36-7.42(m,2H),7.62(d,J=2.1Hz,1H),7.65-7.70(m,2H),7.86(d,J=2.1Hz,1H)IR(CHCl3)3024,2939,1729,1511,1475,1447,1373,1179,1150,1085cm-1 |
I-520 | 粉末1HNMR(CDCl3)δ2.84(s,3H),3.21(s,3H),3.22(s,3H),3.56(s,3H),3.81(s,3H),3.88(s,3H),5.30(s,2H),6.86(s,1H),7.26-7.32(m,1H),7.37-7.42(m,2H),7.65-7.72(m,4H),7.76-7.83(m,1H),7.92(d,J=2.1Hz,1H),8.60-8.63(m,1H)IR(KBr)3434,3019,2940,1730,1511,1474,1367,1178,1151,1082cm-1 |
I-521 | 粉末1HNMR(CDCl3+CD3OD)δ1.69(s,3H),1.77(s,3H),2.51-2.58(m,2H),3.43(s,3H),3.73(s,3H),4.23(t,J=6.6Hz,2H),6.44(s,1H),6.89-6.95(m,2H),7.24(d,J=1.8Hz,1H),7.46-7.52(m,2H),7.65-7.67(m,1H)IR(KBr)3434,2934,1716,1611,1402,1226,1116,1082,1027cm-1 |
I-522 | m.p.240-243℃1HNMR(CDCl3+CD3OD)δ3.44(s,3H),3.75(s,3H),5.31(s,2H),6.46(s,1H),6.89-6.95(m,2H),7.30-7.31(m,1H),7.35-7.42(m,2H),7.47-7.53(m,2H),7.56(d,J=2.4Hz,1H),7.79-7.86(m,1H),8.65-8.68(m,1H)IR(KBr)3411,2937,1683,1611,1521,1406,1230,1115,1082,1026cm-1 |
I-523 | m.p.136-137℃1HNMR(CDCl3)δ2.25(s,3H),2.29(s,3H),3.12(s,3H),3.20(s,3H),5.18(s,2H),7.11(s,1H),7.14(s,1H),7.23-7.51(m,12H)IR(KBr)1518,1488,1357,1263,1170,1150,1110,970,873,848,809cm-1 |
I-524 | m.p.121-122℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.25(s,3H),2.29(s,3H),3.20(s,3H),3.23(s,3H),4.64(d,J=6.6Hz,2H),5.52(t,J=6.6Hz,1H),7.06(d,J=8.4Hz,1H),7.11(s,1H),7.14(s,1H),7.24(d,J=2.1Hz,1H),7.31-7.45(m,5H)IR(KBr)1518,1487,1363,1170,1150,1108,970,869,848,808cm-1 |
I-525 | m.p.149-151℃1HNMR(CDCl3)δ1.77(s,3H),1.83(d,J=0.6Hz,3H),2.26(s,3H),2.28(s,3H),4.62(d,J=6.9Hz,2H),4.80(s,1H),5.53(m,1H),5.72(s,1H),6.82(dd,J=2.1,8.4Hz,1H),6.85-6.94(m,3H),8.96(d,J=2.1Hz,1H),7.10(s,1H),7.12(s,1H),7.21-7.28(m,2H)IR(KBr)3521,3395,1612,1584,1522,1490,1457,1285,1263,1242,1200,1170,1125,1014,834cm-1 |
I-526 | 泡沫1HNMR(CDCl3)δ2.43(s,3H),2.76(s,3H),2.90(s,3H),3.22(s,3H),3.56(s,3H),3.80(s,3H),5.30(s,2H),6.28(t,J=3.3Hz,1H),6.42(dd,J=3.3,1.6Hz,1H),6.85(s,1H),7.12,(d,J=8.4Hz,1H),7.32(d,J=8.7Hz,2H),7.34~7.37(m,2H),7.39(d,J=8.7Hz,2H),7.40(d,J=1.8Hz,1H),7.69(d,J=8.7Hz,2H),7.78(d,J=8.7Hz,2H)IR(Nujol)1608,1597,1519,1480,1464,1176,1152,1087,972,875,817,798cm-1 |
I-527 | 泡沫1HNMR(CDCl3)δ2.96(s,3H),3.21(s,3H),3.37(s,3H),3.52(s,3H),3.77(s,3H),5.58(s,2H),6.84(s,1H),7.19(d,J=8.4Hz,1H),7.24~7.28(m,4H),7.31,(dd,J=8.4,1.8Hz,1H),7.33(d,J=1.8Hz,1H),7.38(d,J=8.7Hz,2H),7.67(d,J=8.7Hz,2H)IR(Nujol)1664,1609,1519,1480,1457,1176,1151,1079,970,947,876,798,748cm-1 |
I-528 | 泡沫1HNMR(CDCl3)δ2.73(s,3H),2.94(s,3H),3.21(s,3H),3.33(t,J=6.3Hz,2H),3.55(s,3H),3.77(s,3H),4.55(t,J=6.3Hz,2H),6.83(s,1H),7.14(d,J=8.1Hz,1H),7.18(brdd,J=7.8,5.1Hz,1H),7.33(brd,J=7.8Hz,1H),7.35(dd,J=8.1,1.8Hz,1H),7.37(d,J=1.8Hz,1H),7.38(d,J=8.7Hz,2H),7.65(m,1H),7.67(d,J=8.7Hz,2H),8.56(brd,J=5.1Hz,1H)IR(Nujol)1608,1593,1520,1479,1466,1177,1151,1079,970,872,816,798cm-1 |
I-529 | m.p.203-205℃HNMR(DMSO-d6)δ2.42(s,3H),2.80(s,3H),3.45(s,3H),3.51(s,3H),3.56(s,3H),3.78(s,3H),5.36(s,2H),7.07(s,1H),7.23(s,1H),7.26~7.28(m,3H),7.48,(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)1599,1518,1480,1466,1176,1081,1013,976,870,830,797,755cm-1 |
I-530 | 泡沫1HNMR(CD3OD)δ3.38(s,3H),3.68(s,3H),5.41(s,2H),6.44(s,1H),6.82(dd,J=8.4,2.1Hz,1H),6.85(d,J=8.7Hz,2H),6.93(d,J=2.1Hz,1H),7.06(d,J=8.4Hz,1H),7.27(m,2H),7.46(d,J=8.7Hz,2H),7.60(m,2H)IR(Nujol)3304,161,1590,1522,1488,1458,1254,1115,1074,1046,1014,942,825,745cm-1 |
I-531 | m.p.159-162℃1HNMR(DMSO-d6)δ2.92(s,3H),3.41(s,3H),3.45(s,3H),3.52(s,3H),3.79(s,3H),5.33(s,2H),7.09(s,1H),6.82~7.45(m,3H),7.49(d,J=9.0Hz,2H),7.75(d,J=9.0Hz,2H)IR(Nujol)1604,1519,1481,1469,1235,1171,1154,1085,1012,967,874,849,798cm-1 |
I-532 | m.p.214-216℃1HNMR(DMSO-d6)δ2.84(s,3H),3.42(s,3H),3.45(s,3H),3.52(s,3H),3.73(s,3H),3.79(s,3H),4.99(s,2H),7.08(s,1H),7.24(dJ=9.3Hz,1H),7.29(dd,J=9.3,1.8Hz,1H),7.90(d,J=1.8Hz,1H),7.48(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)1767,1606,1521,1481,1463,1216,1175,1151,1080,1013,977,946,878,821,798cm-1 |
I-533 | m.p.225-227℃1HNMR(DMSO-d6)δ2.86(s,3H),3.45(s,3H),3.46(s,3H),3.52(s,3H),3.78(s,3H),4.46(s,2H),7.08(s,1H),7.20(d,J=8.4Hz,1H),7.28~7.32(m,2H),7.48(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)3340,1677,1619,1519,1477,1463,1443,1176,1150,1088,971,871,829,794cm-1 |
I-534 | 泡沫1HNMR(DMSO-d6)δ2.96(s,3H),3.45(s,3H),3.47(s,3H),3.52(s,3H),3.79(s,3H),4.64(s,2H),7.08(s,1H),7.18(d,J=8.4Hz,1H),7.31(dd,J=8.4,1.8Hz,1H),7.34(d,J=1.8Hz,1H),7.48(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)3464,3362,1693,1606,1520,1481,1176,1151,1080,876,822,799cm-1 |
I-535 | m.p.163-165℃1HNMR(CDCl3)δ2.73(s,3H),3.16(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),4.85(dd,J=1.5,1.5,5.4Hz,2H),5.25(s,2H),5.31,(ddd,J=1.5,3.0,10.5,Hz,1H),5.43(ddd,J=1.5,3.0,17.1Hz,1H),6.05(ddd,J=5.4,10.5,17.1Hz,1H),6.84(s,1H),7.11(d,J=8.7Hz,1H),7.34(dd,J=2.1,8.7Hz,1H),7.38(d,J=8.4Hz,2H),7.41(d,J=2.1Hz,1H),7.56(d,J=8.4Hz,2H),7.67(d,J=8.4Hz,2H),8.11(d,J=8.4Hz,2H)IR(KBr)1718,1612,1519,1481,1365,1273,1177,1151,1119,1080,1015,969,876cm-1 |
I-536 | m.p.115-117℃1HNMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.21(s,3H),3.55(s,3H),3.68(s,2H),3.78(s,3H),4.61(ddd,J=1.5,1.5,5.7Hz,2H),5.17(s,2H),5.23,(ddd,J=1.5,3.0,10.5,Hz,1H),5.28(ddd,J=1.5,3.0,16.8Hz,1H),5.91(ddd,J=5.7,10.5,16.8Hz,1H),6.84(s,1H),7.13(d,J=8.4Hz,1H),7.33(d,J=8.1Hz,2H),7.34(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.4Hz,2H),7.40(d,J=2.1Hz,1H),7.42(d,J=8.1Hz,2H),7.68(d,J=8.4Hz,2H)IR(KBr)1734,1609,1520,1481,1365,1236,1177,1151,1119,1079,970,876,797cm-1 |
I-537 | m.p.227-229℃1HNMR(CDCl3)δ2.73(s,3H),3.16(s,3H),3.21(s,3H),3.54(s,3H),3.77(s,3H),5.26(s,2H),6.83(s,1H),7.11(d,J=12.3Hz,2H),7.32(s,1H),7.37(d,J=12.3Hz,2H),7.41(s,1H),7.57(d,J=12.3Hz,1H),7.66(d,J=12.3Hz,2H),8.13(d,J=12.3Hz,2H)IR(KBr)3430,1694,1612,1519,1481,1365,1177,1151,1079,875,798cm-1 |
I-538 | m.p.149-151℃1HNMR(CDCl3)δ2.66(s,3H),3.13(s,3H),3.21(s,3H),3.55(s,3H),3.68(s,2H),3.77(s,3H),5.17(s,2H),6.84(s,1H),7.13(d,J=8.4Hz,1H),7.30-7.55(m,4H),7.38(d,J=8.4Hz,2H),7.67(d,J=8.4Hz,2H),7.67(m,2H)IR(KBr)3423,1716,1610,1519,1481,1365,1235,1177,1151,1119,1080,876,798cm-1 |
I-539 | m.p.144-146℃1HNMR(CDCl3)δ2.32(s,3H),2.69(s,3H),3.14(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.18(s,2H),6.84(s,1H),7.14(d,J=8.7Hz,2H),7.15(d,J=8.4Hz,1H),7.34(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.4Hz,2H),7.40(d,J=2.1Hz,1H),7.48(d,J=8.7Hz,2H),7.67(d,J=8.4Hz,2H)IR(KBr)1760,1519,1481,1365,1177,1151,1119,1079,876,797cm-1 |
I-540 | m.p.228-231℃1HNMR(CDCl3)δ2.81(s,3H),3.20(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.30(s,2H),6.85(s,1H),7.11(d,J=8.4Hz,1H),7.35(dd,J=2.1,8.4Hz,1H),7.39(d,J=8.4Hz,2H),7.41(d,J=2.1Hz,1H),7.67(d,J=8.4Hz,2H),7.69(d,J=8.7Hz,2H),8.28(d,J=8.7Hz,2H)IR(KBr)1608,1521,1481,1361,1179,1148,1080,880,799cm-1 |
I-541 | m.p.153-156℃1HNMR(CDCl3)δ1.53(s,9H),2.69(s,3H),3.15(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.19(s,2H),6.84(s,1H),7.10(dd,J=7.5,7.5Hz,1H),7.17(d,J=7.5Hz,1H),7.23(d,J=8.4Hz,1H),7.26(dd,J=7.5,7.5Hz,1H),7.33(d,J=7.5Hz,1H),7.37(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.4Hz,2H),7.40(d,J=2.1Hz,1H),7.67(d,J=8.4Hz,2H)IR(KBr)3405,1724,1519,1480,1366,1236,1177,1153,1080,970,875,798cm-1 |
I-542 | m.p.178-182℃1HNMR(CDCl3)δ2.70(s,3H),3.15(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.14(s,2H),6.76(m,2H),6.84(s,1H),7.19(m,2H),7.26(d,J=8.7Hz,1H),7.37(d,J=2.7Hz,1H),7.36(dd,J=2.7,8.7Hz,1H),7.38(d,J=8.7Hz,2H),7.68(d,J=8.7Hz,2H)IR(KBr)3448,1627,1608,1519,1497,1364,1177,1151,1079,971,876,798cm-1 |
I-543 | m.p.187-189℃1HNMR(CDCl3)δ2.38(s,3H),3.39(s,3H),3.45(s,3H),5.11-5.14(m,3H),5.89(s,1H),6.33(s,1H),6.88-6.94(m,2H),7.20-7.36(m,6H),7.43(d,J=2.1Hz,1H),7.76(d,J=0.6Hz,1H)IR(KBr)3414,2942,1613,1534,1469,1355,1266,1172,1092,1030cm-1 |
I-544 | m.p.207-215℃(dec.)1HNMR(d6-DMSO)δ2.37(s,3H),3.67(brs,2H),4.56(brs,2H),4.90(s,2H),6.14-6.20(m,2H),6.86(d,J=8.7Hz,2H),7.11-7.22(m,4H),7.42(d,J=8.7Hz,2H),7.52(s,1H),8.94(s,1H),9.47(s,1H)IR(KBr)3388,3301,2932,1612,1591,1521,1458,1413,1288,1030cm-1 |
I-545 | m.p.108-110℃1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.49-2.59(m,2H),3.03(s,3H),3.20(s,3H),3.56(s,3H),3.75(s,3H),4.06(t,J=6.6Hz,2H),4.93(s,2H),5.22(m,1H),6.66(s,1H),7.04(d,J=8.7Hz,1H),7.09-7.17(m,2H),7.37(dd,J=2.1,8.7Hz,1H),7.44(d,J=2.1Hz,1H),7.51-7.58(m,2H)IR(KBr)3434,2933,1604,1521,1473,1383,1360,1278,1160,1121,1084,1017cm-1 |
I-546 | m.p.109-110℃1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.48-2.58(m,2H),4.07(t,J=6.6Hz,2H),5.22(m,1H),5.69(s,1H),5.87(s,1H),6.44(s,1H),6.93-6.95(m,2H),7.04-7.06(m,1H),7.10-7.18(m,2H),7.58-7.64(m,2H)IR(KBr)3411,2932,1608,1587,1522,1491,1226,1111,1074,1017cm-1 |
I-547 | m.p.141-142℃1HNMR(CDCl3)δ3.03(s,3H),3.57(s,3H),3.75(s,3H),4.90(s,2H),5.16(s,2H),5.65(brs,1H),6.66(s,1H),6.92(dd,J=1.8,8.4Hz,1H),6.99(d,J=8.4Hz,1H),7.06(d,=1.8Hz,1H),7.10-7.17(m,2H),7.35-7.47(m,5H),7.52-7.59(m,2H)IR(KBr)3529,3439,2932,1601,1518,1477,1461,1380,1251,1224,1157,1113,1094,1076cm-1 |
I-548 | m.p.133-136℃1HNMR(CDCl3)δ2.98(s,3H),3.12(s,3H),3.56(s,3H),3.75(s,3H),4.94(s,2H),5.18(s,2H),6.67(s,1H),7.09-7.17(m,3H),7.34-7.49(m,7H),7.51-7.58(m,2H)IR(KBr)3434,2941,1598,1519,1481,1383,1365,1279,1231,1164,1099,1081cm-1 |
I-549 | m.p.161-162℃1HNMR(CDCl3)δ3.10(s,3H),3.42(s,3H),3.76(s,3H),5.17(s,2H),6.05(s,1H),6.44(s,1H),7.11-7.20(m,3H),7.33-7.50(m,7H),7.52(d,J=2.1Hz,1H),7.57-7.65(m,2H)IR(KBr)3488,2938,1613,1523,1486,1290,1223,1107,1071,1012cm-1 |
I-550 | m.p.113-115℃1HNMR(CDCl3)δ2.37(s,3H),2.98(s,3H),3.11(s,3H),3.56(s,3H),3.75(s,3H),4.93(s,2H),5.13(s,2H),6.66(s,1H),7.09-7.17(m,3H),7.18-7.23(m,2H),7.32-7.39(m,3H),7.45(d,J=1.8Hz,1H),7.51-7.58(m,2H)IR(KBr)3434,2934,1738,1601,1520,1478,1466,1376,1356,1236,1159,1109,1070,1014cm-1 |
I-551 | m.p.138-140℃1HNMR(CDCl3)δ2.38(s,3H),3.04(s,3H),3.57(s,3H),3.74(s,3H),4.90(s,2H),5.11(s,2H),5.63(s,1H),6.66(s,1H),6.91(dd,J=2.1,8.4Hz,1H),6.99(d,J=8.4Hz,1H),7.05(d,J=1.8Hz,1H),7.08-7.17(m,2H),7.22(d,J=7.8Hz,2H),7.33(d,J=7.8Hz,2H),7.52-7.59(m,2H)IR(KBr)3446,2934,1601,1518,1476,1461,1379,1252,1224,1158,1092,1011cm-1 |
I-552 | m.p.188-190℃1HNMR(CDCl3)δ2.38(s,3H),3.10(s,3H),3.42(s,3H),3.75(s,3H),5.12(s,2H),6.04(s,1H),6.43(s,1H),7.11-7.25(m,5H),7.35(d,J=7.8Hz,2H),7.42(dd,J=2.4,8.7Hz,1H),7.51(d,J=2.4Hz,1H),7.57-7.65(m,2H)IR(KBr)3433,2963,1611,1523,1485,1355,1282,1226,1163,1106,1071cm-1 |
I-553 | m.p.149-150℃1HNMR(CDCl3)δ3.13(s,3H),3.21(s,3H),5.20(s,2H),7.17(d,J=8.4Hz,1H),7.24(m,1H),7.36-7.54(m,9H),7.58(dd,J=1.2,2.4Hz,1H),7.60-7.67(m,2H)IR(KBr)1524,1485,1354,1292,1263,1181,1150,1114,977,869,858.850,812,796cm-1 |
I-554 | m.p.92-93℃1HNMR(CDCl3)δ1.69(s,3H),1.74(d,J=1.2Hz,3H),2.25(s,3H),2.28(s,3H),2.56(dt,J=6.6,7.2Hz,2H),3.20(s,3H),3.21(s,3H),4.07(t,J=7.2Hz,2H),5.22(m,1H),7.05(d,J=8.4Hz,1H),7.11(s,1H),7.13(s,1H),7.25(dd,J=2.1,8.4Hz,1H),7.31-7.43(m,5H)IR(KBr)1518,1488,1355,1293,1264,1169,1151,1109,970,872,818cm-1 |
I-555 | m.p.126-127℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.20(s,3H),3.23(s,3H),4.65(d,J=6.6Hz,2H),5.50(m,1H),7.10(d,J=8.7Hz,1H),7.18-7.27(m,2H),7.36-7.43(m,2H),7.50(dd,J=1.5,8.7Hz,1H),7.55(d,J=1.5Hz,1H),7.60-7.66(m,2H)IR(KBr)1527,1489,1359,1295,1266,1177,1153,1118,974,894,874cm-1 |
I-556 | m.p.154-155℃1HNMR(CDCl3)δ2.25(s,3H),2.28(s,3H),2.38(s,3H),3.11(s,3H),3.20(s,3H),5.13(s,2H),7.11(s,1H),7.14(s,1H),7.19-7.28(m,4H),7.3 1-7.43(m,7H)IR(KBr)1520,1487,1365,1284,1260,1192,1172,1152,1108,967,867,809,795cm-1 |
I-557 | m.p.112-113℃1HNMR(CDCl3)δ1.69(s,3H),1.76(s,3H),2.26(s,3H),2.27(s,3H),2.54(dt,J=7.2,6.9Hz,2H),4.07(t,J=6.9Hz,2H),4.86(s,1H),5.23(m,1H),5.71(s,1H),6.82(dd,J=2.1,8.4Hz,1H),685-6.93(m,3H),6.96(d,J=2.1Hz,1H),7.10(s,1H),7.12(s,1H),7.22-7.27(m,2H)IR(KBr)3380.1613,1586,1523,1490,1471,1431,1391,1293,1261,1246,1205,1171,1130,836cm-1 |
I-558 | m.p.141-142℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),4.63(d,J=6.9Hz,2H),5.06(s,1H),5.52(m,1H),5.75(s,1H),6.89-6.97(m,3H),7,07(dt,J=8.4,1.8Hz,1H),7.14-7.23(m,3H),7.44-7.51(m,2H)IR(KBr)3429,1612,1594,1531,1489,1467,1449,1401,1259,1213,1169,1132,835,781cm-1 |
I-559 | m.p.179-180℃1HNMR(CDCl3)δ2.26(s,3H),2.28(s,3H),2.39(s,3H),4.81(s,1H),5.11(s,2H),5.70(s,1H),6.83(dd,J=2.1,8.4Hz,1H),6.86-6.91(m,2H),6.98(d,J=8.4Hz,1H),6.98(d,J=2.1Hz,1H),7.10(s,1H),7.12(s,1H),7.21-7.28(m,4H),7.321.38(m,2H)IR(KBr)3317,1609,1520,1489,1426,1378,1247,1206,1175,1124,1006,792cm-1 |
I-560 | 泡沫1HNMR(DMSO-d6)δ3.74(s,3H),3.75(s,3H),4.62(d,J=5.0Hz,2H),5.02(t,J=5.0Hz,1H),5.19(s,2H),6.94(s,1H),6.99(s,1H),7.06(d,J=8.0Hz,1H),7.22(ddd,J=8.6,2.0,0.8Hz,1H),7.32-7.52(m,8H),7.57(d,J=2.4Hz,1H),9.91(brs,1H)IR(KBr)3257,1525,1491,1464,1453,1382,1207,1035,764,737cm-1 |
I-561 | m.p.147-148℃1HNMR(CDCl3)δ3.27(s,3H),3.79(s,3H),3.82(s,lH),5.26(s,2H),6.92(s,1H),6.95(s,1H),7.13(d,J=8.7Hz,1H),7.35-7.50(m,8H),7.80(dd,J=8.7,2.7Hz,1H),8.05(d,J=2.7Hz,1H),10.62(s,1H)IR(KBr)1682,1606,1489,1377,1345,1261,1209,1168,1119,1038,871,832cm-1 |
I-562 | m.p.189-191℃1HNMR(DMSO-d6)δ3.53(s,3H),3.80(s,3H),3.80(s,3H),5.27(s,2H),7.05(s,1H),7.10(s,1H),7.25(d,J=8.7Hz,1H),7.30-7.59(m,7H),7.66(dd,J=11.7,2.1Hz,1H),7.67(dd,J=8.7,2.3Hz,1H),7.84(d,J=2.3Hz,1H),12.7(brs,1H)IR(KBr)3433,1705,1492,1371,1250,1207,1168,1033,868cm-1 |
I-563 | m.p.204-207℃1HNMR(CDCl3)δ1.36(s,9H),3.20(s,3H),3.41(s,3H),3.74(s,3H),5.15(s,2H),5.65(s,1H),5.77(s,1H),6.80(s,1H),6.83(dd,J=8.4,2.0Hz,1H),6.96(d,J=2.0Hz,1H),6.98(d,J=8.4Hz,1H),7.34-7.45(m,7H),7.68(d,J=8.7Hz,2H)IR(KBr)3408,3337,1692,1498,1474,1466,1347,1251,1150,870,855cm-1 |
I-564 | m.p.179-182℃1HNMR(DMSO-d6)δ3.76(s,3H),3.76(s,3H),5.26(s,2H),6.99(s,1H),7.00(t,J=8.7Hz,1H),7.01(s,1H),7.22(ddd,J=8.7,2.4Hz,J=1.2Hz,1H),7.24(d,J=8.9Hz,1H),7.32-7.54(m,6H),7.65(dd,J=8.9,2.4Hz,1H),7.82(d,J=2.4Hz,1H),9.91(s,1H),12.6(brs,1H)IR(KBr)3422,3277,1726,1526,1491,1416,1396,1284,1210,1031cm-1 |
I-565 | m.p.178-180℃1HNMR(DMSO-d6)δ3.30(s,3H),3.43(s,3H),3.61(s,3H),4.31(s,2H),5.14(s,2H),6.25(s,1H),6.61(dd,J=8.4,1.9Hz,1H),7.05(d,J=8.4Hz,1H),7.33-7.44(m,6H),7.50-7.54(m,2H),7.70(d,J=8.7Hz,2H),9.08(s,1H)IR(KBr)3435,3378,1593,1518,1481,1360,1245,1147,1119,1010,871cm-1 |
I-566 | 泡沫1HNMR(DMSO-d6)δ3.27(s,3H),3.59(s,H),4.21(s,2H),5.13(s,2H),6.17(s,1H),6.60(dd,J=8.3,1.4Hz,1H),6.70(d,J=1.4Hz,1H),6.82(d,J=8.4Hz,2H),7.03(d,J=8.3Hz,1H),7.33-7.53(m,7H),9.07(brs,1H),9.45(brs,1H)IR(KBr)3390,1609,1592,1522,1484,1247,1227,1119,1011,812cm-1 |
I-567 | m.p.146-148℃1HNMR(DMSO-d6)δ1.64(s,3H),1.70(s,3H),2.44(q,J=6.9Hz,2H),3.53(s,3H),3.78(s,3H),3.80(s,3H),4.05(t,J=6.9Hz,2H),5.26(t,J=6.9Hz,2H),7.05(s,1H),7.10(s,1H),7.19(d,J=8.4Hz,1H),7.50(dd,J=8.4,2.0Hz,1H),7.57(t,J=8.3Hz,1H),7.65(ddd,J=8.3,1.9,0.9Hz,1H),7.66(dd,J=11.9,1.9Hz,1H),7.79(d,J=2.0Hz,1H),12.5(brs,1H)IR(KBr)3434,3299,1727,1489,1375,1341,1209,1172,1033,851,824cm-1 |
I-568 | m.p.179-181℃1HNMR(CDCl3)δ1.31(s,9H),3.11(s,3H),3.20(s,3H),3.39(s,3H),3.74(s,3H),5.16(s,2H),5.98(s,1H),6.79(s,1H),7.09(d,J=8.5Hz,1H),7.29(dd,J=8.5,1.9Hz,1H),7.35-7.49(m,8H),7.66(d,J=8.7Hz,2H)IR(KBr)3404,3341,1690,1517,1465,1369,1348,1174,1151,869,814cm-1 |
I-569 | m.p.189-191℃1HNMR(DMSO-d6)δ3.31(s,3H),3.33(s,3H),3.43(s,3H),3.64(s,3H),4.48(s,2H),5.25(s,2H),6.28(s,1H),7.24(dd,J=9.0,2.0Hz,1H),7.24(d,J=2.0Hz,1H),7.34-7.46(m,6H),7.52-7.55(m,2H),7.70(d,J=9.0Hz,2H)IR(KBr)3490,3392,1596,1518,1483,1364,1150,872,813cm-1 |
I-570 | m.p.194-196℃1HNMR(CDCl3)δ3.07(s,3H),3.22(s,3H),3.36(s,3H),3.77(s,3H),5.16(s,2H),6.92(s,1H),7.13(d,J=8.6Hz,1H),7.25(dd,J=8.6,2.1Hz,1H),7.29(d,J=2.1Hz,1H),7.36.7.47(m,7H),7.63(brs,1H),7.67(d,J=8.4Hz,2H)IR(KBr)3433,3329,1737,1518,1476,1369,1168,1148,878cm-1 |
I-571 | m.p.184-186℃1HNMR(CDCl3)δ2.31(s,3H),2.38(s,3H),3.12(s,3H),3.45(s,3H),3.58(s,3H),3.76(s,3H),5.14(s,2H),6.95(s,1H),7.11-7.23(m,5H),7.34-7.37(m,4H),7.57(dd,J=8.7,2.4Hz,1H),7.66(d,J=2.4Hz,1H)IR(CHCl3)2952,1732,1614,1599,1518,1467,1445,1370,1290,1256,1169,1117,1081,1064,1003,973,905,827cm-1 |
I-572 | m.p.218-220℃1HNMR(CDCl3)δ2.38(s,3H),3.12(s,3H),3.44(s,3H),3.63(s,3H),3.76(s,3H),5.14(s,2H),6.80-6.83(m,2H),6.94(s,1H),7.14(d,J=8.7Hz,1H),7.21-7.23(m,4H),7.35-7.37(11,2H),7.56(dd,J=8.7,2.4Hz,1H),7.66(d,J=2.4Hz,1H)IR(CHCl3)3596,2939,1720,1613,1522,1466,1445,1370,1346,1291,1258,1183,1172,1116,1081,1064,1003,973,904,866,837cm-1 |
I-573 | m.p.197-199℃1HNMR(CD3OD)δ3.19(s,3H),3.43(s,3H),3.76(s,3H),5.25(s,2H),7.06-7.12(m,3H),7.32-7.43(m,6H),7.52-7.54(m,2H),7.60(dd,J=8.4,2.4Hz,1H),7.66(d,J=2.4Hz,1H)IR(KBr)3421,2941,1738,1708,1643,1519,1472,1354,1297,1259,1228,1171,1119,1081,1063,1001,958,920,871,826,755,697,524cm-1 |
I-574 | m.p.151-153℃1HNMR(CDCl3)δ2.39(s,3H),3.44(s,3H),3.64(s,3H),3.74(s,3H),5.12(s,2H),5.78(br,2H),6.78-6.81(m,2H),6.94(s,1H),6.99(d,J=8.4Hz,1H),7.15-7.25(m,6H),7.33-7.36(m,2H)IR(CHCl3)3595,3541,2952,1730,1612,1591,1521,1474,1395,1345,1323,1290,1258,1173,1129,1081,1063,1004,901,863,836cm-1 |
I-575 | m.p.195-196℃1HNMR(CD3OD)δ2.34(s,3H),3.40(s,3H),3.72(s,3H),5.16(s,2H),6.75-6.78(m,2H),6.96(s,1H),7.02(s,1H),7.14-7.21(m,6H),7.36-7.39(m,2H)IR(KBr)3530,3398,2942,1708,1610,1593,1520,1465,1373,1334,1256,1233,1127,1078,1056,996,960,864,834,791,755,690,651,605,534cm-1 |
I-576 | m.p.82-84℃1HNMR(CDCl3)δ1.70(s,3H),1.75(s,3H),2.54-2.59(m,2H),3.24(s,3H),3.50(s,3H),3.77(s,3H),4.10(t,J=6.9Hz,2H),5.23(m,1H),7.07-7.12(m,4H),7.23-7.28(m,2H),7.57(dd,J=8.7,2.4Hz,1H),7.63(d,J=2.4Hz,1H),9.99(s,1H)IR(CHCl3)2936,1697,1604,1591,1518,1469,1445,1371,1331,1294,1232,1172,1159,1123,1093,1005,964cm-1 |
I-577 | m.p.126-128℃1HNMR(CD3OD)δ1.70(s,3H),1.74(d,J=0.9Hz,3H),2.53-2.61(m,2H),3.25(s,3H),3.44(s,3H),3.75(s,3H),4.13(t,J=6.3Hz,2H),5.29(m,1H),7.04-7.11(m,3H),7.24(d,J=8.7Hz,1H),7.33-7.38(m,2H),7.58-7.65(m,2H)IR(KBr)3432,2940,2566,1735,1711,1646,1613,1519,1470,1447,1366,1297,1264,1228,1172,1118,1081,1063,1001,962,920,898,871,828,796,695,524cm-1 |
I-578 | m.p.202-204℃1HNMR(CDCl3)δ3.13(s,3H),3.45(s,3H),3.61(s,3H),3.76(s,3H),5.19(s,2H),6.95(s,1H),7.05-7.11(m,2H),7.14(d,J=8.7Hz,1H),7.30-7.49(m,7H),7.57(dd,J=8.7,2.4Hz,1H),7.67(d,J=2.4Hz,1H)IR(CHCl3)2952,1731,1603,1519,1472,1445,1371,1345,1291,1172,1159,1117,1081,1064,1004,972,960,904cm-1 |
I-579 | m.p.197-199℃1HNMR(CDCl3)δ2.71(s,3H),3.56,(s,3H),3.75(s,3H),5.18(s,2H),5.72,(s,1H),6.86(s,1H),7.00(d,J=8.4Hz1H),7.12-7.18(m,3H),7.24(d,J=2.1Hz,1H),7.38-7.46(m,7H)IR(CHCl3)3543,2939,1602,1521,1482,1465,1394,1370,1328,1254,1178,1159,1130,1081,1005,964,840,816cm-1 |
I-580 | m.p.199-201℃1HNMR(CD3OD)δ3.40(s,3H),3.73(s,6H),5.22(s,2H),7.00(s,1H),7.03-7.11(m,4H),7.17(m,1H),7.31-7.41(m,5H),7.49-7.52(m,2H)IR(KBr)3527,3434,2940,1701,1591,1518,1465,1380,1335,1320,1291,1270,1222,1161,1130,1078,1056,1002,916,868,837,747,698,633,599,526,480cm-1 |
I-581 | m.p.122-123℃1HNMR(CDCl3)δ1.78(s,3H),1.82(s,3H),3.25(s,3H),3.50(s,3H),3.76(s,3H),4.66(d,J=6.9Hz,2H),5.52(m,1H),7.09-7.14(m,4H),7.23-7.27(m,2H),7.56(dd,J=8.7,2.1Hz,1H),7.63(d,J=2.1Hz,1H),9.99(s,1H)IR(CHCl3)2938,1679,1604,1591,1517,1469,1445,1371,1331,1292,1172,1159,1122,1092,1004,973cm-1 |
I-582 | m.p.158-159℃1HNMR(CDCl3)δ2.69(s,3H),3.13(s,3H),3.57(s,3H),3.76(s,3H),5.19(s,2H),6.85(s,1H),7.13-7.18(m,3H),7.37-7.49(m,7H),7.56(dd,J=9.0,2.1Hz,1H),7.62(d,J=2.1Hz,1H)IR(CHCl3)2939,1603,1521,1482,1464,1294,1253,1177,1119,1082,1003,963,876,842cm-1 |
I-583 | m.p.145-147℃1HNMR(CDCl3)δ2.68(s,3H),3.54(s,3H),3.56(s,3H),3.75(s,3H),5.21(s,2H),5.27(s,2H),6.85(s,1H),7.00(d,J=8.7Hz,1H),7.13-7.23(m,3H),7.33-7.49(m,8H)IR(CHCl3)2938,1731,1603,1520,1482,1370,1249,1178,1158,1134,1081,1004,961,840,815cm-1 |
I-584 | m.p.160-162℃1HNMR(CDCl3)δ3.47(s,3H),3.74(s,3H),5.18(s,2H),5.72(s,1H),6.00(s,1H),6.46(s,1H),7.01(d,J=8.4Hz,1H),7.10-7.19(m,3H),7.27(d,J=2.1Hz,1H),7.36-7.48(m,7H)IR(CHCl3)3540,2938,1603,1568,1522,1490,1464,1416,1396,1325,1263,1158,1111,1072,1002,838cm-1 |
I-585 | m.p.133-134℃1HNMR(CD3OD)δ1.80(d,J=0.9Hz,3H),1.82(d,J=0.9Hz,3H),3.26(s,3H),3.44(s,3H),3.76(s,3H),4.71(d,J=6.9Hz,2H),5.55(m,1H),7.06-7.12(m,3H),7.26(d,J=8.7Hz,1H),7.34-7.36(m,2H),7.58-7.63(m,2H)IR(KBr)3422,2939,1736,1702,1603,1519,1472,1368,1293,1228,1187,1173,1117,1081,1061,1003,975,961,920,827,759,701,523cm-1 |
I-586 | m.p.152-153℃1HNMR(CDCl3)δ1.69(s,3H),1.74(d,J=0.9Hz,3H),2.55-2.57(m,2H),3.23(s,3H),3.44(s,3H),3.60(s,3H),3.77(s,3H),4.09(t,J=6.6Hz,2H),5.22(m,1H),6.95(s,1H),7.05-7.11(m,3H),7.30-7.35(m,2H),7.57(dd,J=8.7,2.4Hz,1H),7.64(d,J=2.4Hz,1H)IR(CHCl3)2938,1731,1601,1519,1469,1445,1370,1345,1291,1172,1159,1117,1081,1064,1004,973,904,864,840cm-1 |
I-587 | m.p.132-133℃1HNMR(CDCl3)δ3.44(s,3H),3.61(s,3H),3.75(s,3H),5.18(s,2H),5.71(s,1H),6.95(s,1H),6.99-7.10(m,3H),7.17(dd,J=8.4,2.1Hz,1H),7.25-7.47(m,8H)IR(CHCl3)3542,2952,2938,1731,1597,1519,1474,1392,1345,1321,1290,1266,1159,1130,1080,1063,1000,900,862,839cm-1 |
I-588 | m.p.92-94℃1HNMR(CDCl3)δ1.69(d,J=0.6Hz,3H),1.76(d,J=1.2Hz,3H),2.51-2.58(m,2H),3.45(s,3H),3.75(s,3H),4.09(t,J=6.9Hz,2H),5.23(m,1H),5.70(br,1H),6.92(d,J=8.4Hz,1H),6.97(s,1H),7.05-7.10(m,2H),7.16(dd,J=8.4,2.1Hz,1H),7.23(d,J=2.1Hz,1H),7.33-7.38(m,2H)IR(KBr)3534,3432,2936,1713,1597.1519,1473,1377,1322,1260,1231,1158,1130,1081,1063,1004,961,919,837,808,791,754,705,521cm-1 |
I-589 | m.p.120-122℃1HNMR(CDCl3)δ1.69(s,3H),1.76(s,3H),2.51-2.58(m,2H),3.44(s,3H),3.61(s,3H),3.75(s,3H),4.09(t,J=6.6Hz,2H),5.23(m,1H),5.73(s,1H),6.92(d,J=8.4Hz,1H),6.96(s,1H),7.04-7.10(m,2H),7.16(dd,J=8.1,1.8Hz,1H),7.23(d,J=1.8Hz,1H),7.31-7.36(m,2H)IR(CHCl3)3541,2937,1731,1598,1519,1471,1391,1345,1323,1290,1265,1159,1130,1080,1063,1005,839cm-1 |
I-590 | m.p.154-156℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.24(s,3H),3.45(s,3H),3.61(s,3H),3.76(s,3H),4.64(d,J=7.2Hz,2H),5.51(m,1H),6.95(s,1H),7.05-7.11(m,3H),7.31-7.35(m,2H),7.57(dd,J=8.7,2.4Hz,1H),7.64(d,J=2.4Hz,1H)IR(CHCl3)2938,1731,1602,1519,1472,1445,1370,1345,1290,1186,1116,1080,1064,1003,973,904,840cm-1 |
I-591 | m.p.181-182℃1HNMR(CD3OD)δ1.77(s,3H),1.80(d,J=0.9Hz,3H),3.42(s,3H),3.74(s,3H),4.65(d,J=6.9Hz,2H),5.55(m,1H),6.99-7.11(m,5H),7.15(d,J=2.1Hz,1H),7.32-7.36(m,2H)IR(KBr)3529,3424,2937,1714,1598,1519,1473,1417,1372,1336,1321,1258,1235,1157,1129,1080,1062,1004,989,917,854,839,807,791,752,703cm-1 |
I-592 | m.p.109-110℃1HNMR(CDCl3)δ1.78(s,3H),1.83(s,3H),3.44(s,3H),3.61(s,3H),3.75(s,3H),4.63(d,J=6.6Hz,2H),5.53(m,1H),5.72(s,1H),6.94(d,J=8.1Hz,1H),6.96(s,1H),7.04-7.10(m,2H),7.16(Jd,J=8.4,2.1Hz,1H),7.23(d,J=2.1Hz,1H),7.31-7.36(m,2H)IR(CHCl3)3538,2938,1731,1598,1519,1473,1391,1345,1290,1264,1159,1129,1080,1063,1004,900,862,839cm-1 |
I-593 | m.p.185-187℃1HNMR(CDCl3)δ3.78(s,3H),3.80(s,3H),4.82(s,1H),6.61(m,1H),6.88-6.93(m,2H),6.96(s,1H),7.04(s,1H),7.23-7.25(m,1H),7.45(d,J=0.9Hz,1H),7.48-7.53(m,2H),7.83(d,J=0.9Hz,1H),8.18(brs,1H)IR(KBr)3600-3200(br),1611,1523,1496,1464,1447,1388,1268,1239,1202,1046,1025cm-1 |
I-594 | m.p.188-189℃1HNMR(CDCl3)δ3.19(s,3H),3.79(s,3H),3.81(s,3H),6.61-6.62(m,1H),6.96(s,1H),7.06(s,1H),7.24-7.26(m,1H),7.33-7.37(m,2H),7.45(brs,2H),7.64-7.68(m,2H),7.84(d,J=0.9Hz,1H),8.21(brs,1H)IR(KBr)3600-3200(br),1518,1494,1465,1419,1389,1351,1331,1314,1213,1177,1145,1051,1027cm-1 |
I-595 | m.p.98-101℃1HNMR(CDCl3)δ1.77(s,3H),1.78(s,3H),1.82(s,3H),1.85(s,3H),3.78(s,3H),3.79(s,3H),4.56(d,J=6.9Hz,2H),4.72(d,J=6.9Hz,2H),5.39-5.44(m,1H),5.52-5.57(m,1H),6.53(d,J=3.0Hz,1H),6.97-7.03(m,4H),7.12(d,J=3.3Hz,1H),7.38(d,J=8.4Hz,1H),7.45(dd,J=1.8,8.7Hz,1H),7.52-7.57(m,2H),7.81(d,J=1.5Hz,1H)IR(KBr)3600-2800(br).1606,1498,1476,1463,1382,1262,1241,1206,1177,1052,1030cm-1 |
I-596 | m.p.207-210℃1HNMR(CDCl3)δ3.19(s,3H),3.80(s,3H),3.81(s,3H),5.50(s,2H),6.65(d,J=3.0Hz,1H),6.81(d,J=7.8Hz,1H),6.96(s,1H),7.05(s,1H),7.19-7.22(m,1H),7.25-7.45(m,6H),7.54-7.60(m,1H),7.64-7.69(m,2H),7.86(brs,1H),8.61-8.64(m,1H)IR(KBr)3600-3200(br),1496,1478,1364,1347,1210,1176,1155,1052,1028cm-1 |
1-597 | m.p.222-224℃1HNMR(CDCl3)δ2.36(s,3H),2.53(s,3H),3.77(s,3H),3.78(s,3H),6.69(dd,J=0.9,4.2Hz,1H),6.95(s,1H),6.96(s,1H),7.23-7.28(m,2H),7.31-7.35(m,2H),7.51-7.54(m,3H),7.59(d,J=3.3Hz,1H),7.73(d,J=1.2Hz,1H),7 80-7.84(m,2H),8.03(d,J=1.2Hz,1H)IR(KBr)3600-3200(br),1509,1487,1464,1444,1366,1208,1172,1129,1092,1049,1028cm-1 |
I-598 | m.p.126-127℃1HNMR(CDCl3)δ1.69(s,3H),1.71(d,J=0.9Hz,3H),2.56(dt,J=6.6,6.9Hz,2H),3.20(s,3H),3.22(s,3H),4.08(t,J=6.9Hz,2H),5.21(m,1H),7.08(d,J=8.4Hz,1H),7.18-7.27(m,2H),7.36-7.43(m,2H),7.50(dd,J=1.8,8.4Hz,1H),7.56(d,J=1.8Hz,1H),7.59-7.66(m,2H)IR(KBr)1528,1488,1469,1395,1362,1342,1297,1265,1201,1176,1152,1116,968,890,872,818cm-1 |
I-599 | m.p.169-170℃1HNMR(DMSO-d6)δ2.32(s,3H),3.37(s,3H),3.45(s,3H),5.23(s,2H),7.23(d,J=7.8Hz,2H),7.37-7.44(m,3H),7.47-7.53(m,2H),7.56-7.66(m,4H),7.75(d,J=7.5Hz,2H)IR(KBr)1525,1485,1366,1355,1291,1262,1181,1150,1116,969,869,811cm-1 |
I-600 | m.p.123-124℃1HNMR(CDCl3)δ1.68(s,3H),1.75(d,J=0.9Hz,3H),2.53(dt,J=7.2,6.9Hz,2H),4.07(t,J=6.9Hz,2H),4.91(s,1H),5.22(m,1H),5.72(s,1H),6.89-6.95(m,2H),7.07(m,1H),7.14-7.22(m,4H),7.44-7.51(m,2H)IR(KBr)3448,1612,1593,1530,1489,1475,1401,1262,1212,1181,1169,1132,839,779cm-1 |
I-601 | m.p.184-185℃1HNMR(DMSO-d6)δ2.31(s,3H),5.13(s,2H),6.85-6.91(m,2H),6.97(m,1H),7.07(d,J=8.4Hz,1H),7.07(d,J=1.8Hz,1H),7.20(d,J=8.1Hz,2H),7.32-7.48(m,6H)IR(KBr)3290,1614,1529,1491,1459,1449,1405,1380,1267,1254,1167,1132,783cm-1 |
I-602 | m.p.141-142℃1HNMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.46(s,3H),3.78(s,3H),4.56(d,J=6.8Hz,2H),5.54(t,J=6.6Hz,1H),6.96-7.26(m,7H),7.61(dd,J=5.2,8.6Hz,2H),9.88(s,1H)IR(KBr)3433,2955,2922,2865,2833,1687,1604,1515,1462,1288,1258,1232,1180,1160,1070,998,845cm-1 |
I-603 | m.p.169-170℃1HNMR(CDCl3)δ2.38(s,3H),3.46(s,3H),3.77(s,3H),5.07(s,2H),7.02-7.38(m,7H),7.61(dd,J=5.4,8.8Hz,2H),9.89(brs,1H)IR(KBr)3433,2936,2840,1698,1517,1462,1251,1233,1067,999,837cm-1 |
I-604 | m.p.120-121℃1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.50-2.57(m,2H),3.46(s,3H),3.77(s,3H),3.98(t,J=7.0Hz.,2H),5.24(t,J=7.0Hz,1H),6.94-7.26(m,7H),7.61(dd,J=5.4,8.8Hz,2H),9.88(brs,1H)IR(KBr)3435,2960,2937,2876,1698,1605,1516,1464,1441,1379,1296,1272,1233,1221,1161,1073,1024,845,807cm-1 |
I-605 | m.p.151-152℃1HNMR(DMSO-d6)δ1.34(s,6H),3.07-3.15(m,1H),3.32(s,3H),3.67(s,3H),3.97-4.08(m,1H),4.28-4.34(m,1H),6.48(s,1H),7.00(d,J=7.8Hz,2H),7.22-7.35(m,4H),7.66(dd,J=3.2,6.0Hz,2H),8.72(brs,1H)IR(KBr)3460,2960,2935,1607,1521,1488,1456,1392,1244,1226,1160,1122,1073,818cm-1 |
I-606 | m.p.164-165℃1HNMR(DMSO-d6)δ2.32(s,3H),3.31(s,3H),3.66(s,3H),5.08(s,2H),6.46(s,1H),6.99(d,J=5.8Hz,2H),7.20-7.38(m,4H),7.65(dd,J=3.6,6.2Hz,2H),8.69(brs,1H)IR(KBr)3367,2940,1605,1519,1484,1466,1449,1390,1229,1181,1158,1059,1006,987,831,817cm-1 |
I-607 | m.p.103-104℃1HNMR(DMSO-d6)δ1.37(s,6H),2.47-2.59(m,2H),3.31(s,3H),3.66(s,3H),3.94-4.05(m,1H),4.26-4.34(m,1H),6.44(s,1H),7.02(d,J=7.6Hz,2H),7.18-7.35(m,4H),7.64(dd,J=3.4,6.6Hz,2H),8.77(brs,1H)IR(KBr)3400,2993,2961,2930,1607,1522,1486,1471,1454,1393,1226,1123,1072,835,819cm-1 |
I-608 | m.p.157-158℃1HNMR(DMSO-d6)δ1.73(s,3H),1.77(s,3H),3.31(s,3H),3.72(s,3H),4.54(d,J=6 9Hz,2H),5.47(t,J=7.2Hz,1H),6.93(d,J=8.7Hz,2H),7.05(s,1H),7.19(d,J=9.0Hz,2H),7.30-7.36(m,2H),7.70(dd,J=5.4,8.7Hz,2H)IR(KBr)3406,2936,1712,1608,1519,1472,1444,1375,1235,839cm-1 |
I-609 | m.p.215-216℃1HNMR(DMSO-d6)δ2.34(s,3H),3.33(s,3H),3.74(s,3H),5.09(s,2H),7.00.7.07(m,3H),7.22-7.39(m,8H),7.73(dd,J=5.6,8.0Hz,2H)IR(KBr)3494,3289,2938,1745,1698,1520,1471,1461,1378,1296,1239,1183,1159,829cm-1 |
I-610 | m.p.169-170℃1HNMR(DMSO-d6)δ1.64(s,3H),1.71(s,3H),2.41-2.46(m,2H),3.32(s,3H),3.73(s,3H),3.97(t,J=6.6Hz,2H),5.23(t,J=7.2Hz,1H),6.93(d,J=8.1Hz,2H),7.05(s,1H),7.20(d,J=7.2Hz,2H),7.30-7.36(m,2H),7.70(dd,J=4.5,7.5Hz,2H)IR(KBr)3424,2933,1701,1609,1519,1471,1379,1294,1248,1061,839cm-1 |
I-611 | m.p.167-168℃1HNMR(CDCl3)δ1.75(s,3H),1.82(s,3H),2.35(s,6H),2.45(s,3H),3.21(s,3H),3.56(s,3H),3.70(s,3H),4.35(d,J=6.9Hz,2H),5.60(t,J=7.2Hz,1H),6.84(s,1H),7.08(s,2H),7.38(d,J=8.7Hz,2H),7.70(d,J=9.0Hz,2H)IR(KBr)3433,2932,1509,1475,1376,1359,1232.,1177,1152,1085,966,874,797cm-1 |
I-612 | m.p.175-176℃1HNMR(CDCl3)δ2.35(s,6H),2.39(s,3H),2.49(s,3H),3.21(s,3H),3.56(s,3h),3.79(s,3H),4.83(s,2H),6.84(s,1H),7.10(s,2H),7.22(d,J=7.5Hz,2H),7.38(d,J=8.4Hz,4H),7.70(d,J=9.0Hz,2H)IR(KBr)3434,2936,1510,1475,1363,1229,1176,1152,1083,964,871,803cm-1 |
I-613 | m.p.138-139℃1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.33(s,6H),2.52-2.55(m,2H),3.21(s,3H),3.56(s,3H),3.78(s,3H),3.79(t,J=6.9Hz,2H),5.27(t,J=6.6Hz,1H),6.83(s,3H),7.08(s,6H),7.38(d,J=8.7Hz,2H),7.70(d,J=9.0Hz,2H)IR(Br)3432,2939,1509,1476,1448,1362,1237,1172,1155,1103,1081,963,873,800cm-1 |
I-614 | m.p.89-90℃1HNMR(DMSO-d6)δ1.74(s,3H),1.77(s,3h),3.36(s,3H),3.67(s,3H),4.22(d,J=3.0Hz,2H),4.56(d,J=6.3Hz,2H),5.48(t,J=5.7Hz,1H),6.93-6.96(m,3H),7.11(d,J=8.7Hz,2H),7.28-7.34(m,2H),7.68(dd,J=6.0,8.7Hz,2H)IR(KBr)3528,3418,2935,1608,1518,1472,1233,1004,836cm-1 |
I-615 | m.p.89-90℃1HNMR(DMSO-d6)δ2.33(s,3H),3.36(s,3H),3.67(s,3H),4.22(d,J=3.9Hz,2H),4.59(t,J=4.2Hz,1H),5.09(s,2H),6.94(s,1H),7.02(d,J=8.4Hz,2H),7.22(d,J=8.4Hz,4H),7.28-7.39(m,4H),7.68(dd,J=5.7,8.4Hz,2H)IR(KBr)3485,2931,1517,1473,1460,1383,1243,1225,1079,1014,1001,834,798cm-1 |
I-616 | oil1HNMR(DMSO-d6)δ1.75(s,3H),1.78(s,3H),2.47-2.52(m,2H),3.39(s,3H),3.71(s,3H),4.25(d,J=3.3Hz,2H),4.49(d,J=6.3Hz,2H),5.46(t,J=5.7Hz,1H),6.91-6.95(m,3H),7.13(d,J=8.4Hz,2H),7.24-7.32(m,2H),7.67(dd,J=5.7,8.4Hz,2H)IB(KBr)3528,3419,2935,1608,1518,1472,1383,1232,1004,837cm-1 |
I-617 | m.p.138-139℃1HNMR(DMSO-d6)δ1.70(s,3H),1.77(s,3H),2.24(s,6H),3.30(s,3H),3.64(s,3H),4.31(d,J=6.9Hz,2H),5.56(t,J=6.6Hz,1H),6.39(s,1H),6.84(d,J=8.4Hz,2H),6.91(s,2H),7.44(d,J=8.4Hz,2H),8.50(s,1H),9.50(s,1H)IR(KBr)3400,2966,2934,1609,1519,1465,1444,1389,1362,1269,1228,1211,1194,1171,1118,1089,1027,953cm-1 |
I-618 | m.p.122-123℃1HNMR(DMSO-d6)δ2.29(s,6H),2.37(s,3H),3.30(s,3H),3.67(s,3H),4.81(s,2H),6.43(s,1H),6.86(d,J=7.5Hz,2H),6.97(s,2H),7.27(d,J=6.9Hz,2H),7.42-7.48(m,2H),8.54(s,1H),9.52(s,1H)IR(KBr)3483,3423,2931,1735,1709,1612,1520,1477,1454,1411,1395,1362,1224,1176,1117,1089,1028cm-1 |
I-619 | m.p.81-82℃1HNMR(DMSO-d6)δ1.70(s,3H),1.76(s,3H),2.18-2.30(m,2H),2.27(s,6H),3.34(s,3H),3.68(s,3H),3.80(t,J=4.5Hz,2H),5.34(t,J=5.1Hz,1H),6.43(s,1H),6.88(d,J=7.5Hz,2H),6.94(s,6H),7.46-7.50(m,2H),8.53(s,1H),9.54(s,1H)IR(KBr)3410,2930,1612,1521,1479,1454,1395,1361,1265,1227,1174,1117,1090,1028,825cm-1 |
I-620 | m.p.161-162℃1HNMR(CDCl3)δ1.32(s,9H),2.38(s,3H),3.10(s,3H),3.20(s,3H),3.39(s,3H),3.74(s,3H),5.12(s,2H),5.96(s,1H),6.79(s,1H),7.09(d,J=8.4Hz,1H),7.21(d,J=7.8Hz,2H),7.28(dd,J=8.4,1.8Hz,1H),7.33-7.38(m,5H),7.67(d,J=8.4Hz,2H)IR(KBr)3398,1718,1518,1472,1366,1173,1151,877,867,813cm-1 |
I-621 | m.p.139-141℃1HNMR(CDCl3)δ1.33(s,9H),1.68(s,3H),1.74(s,3H),2.54(q,J=6.9Hz,2H),3.19(s,3H),3.20(s,3H),3.39(s,3H),3.73(s,3H),4.05(t,J=6.9Hz,2H),5.21(t,J=6.9Hz,1H),5.95(s,1H),6.79(s,1H),7.02(d,J=8.4Hz,1H),7.29(dd,J=8.4,1.9Hz,1H),7.33(d,J=1.9Hz,1H),7.36(d,J=8.7Hz,2H),7.66(d,J=8.7Hz,2H)IR(KBr)3416,1720,1519,1469,1365,1237,1152,1117,975,872,815cm-1 |
I-622 | m.p.197-199℃1HNMR(DMSO-d6)δ2.33(s,3H),3.31(s,6H),3.43(s,3H),3.64(s,3H),3.74(s,3H),4.47(s,2H),5.19(s,2H),6.28(s,1H),7.21-7.25(m,4H),7.35(d,J=8.7Hz,1H),7.40-7.44(m,4H),7.70(d,J=9.0Hz,2H)IR(KBr)3482,3385,1597,1519,1484,1368,1353,1150,872,813cm-1 |
I-623 | m.p.99-101℃1HNMR(DMSO-d6)δ2.32(s,3H),3.27(s,3H),3.59(s,3H),4.21(s,2H),5.08(s,2H),6.17(s,1H),6.58(dd,J=8.0,1.8Hz,1H),6.69(d,J=1.8Hz,1H),6.82(d,J=8.7Hz,2H),7.01(d,J=8.0Hz,1H),7.21(d,J=7.8Hz,2H),7.39(d,J=7.8Hz,2H),7.41(d,J=8.7Hz,2H),9.02(brs,1H),9.45(brs,1H)1R(KBr)3390,1609,1592,1521,1484,1246,1227,1117,1011,810cm-1 |
I-624 | m.p.215-217℃1HNMR(CDCl3+CD3OD)d3.78(s,3H),3.79(s,3H),5.49(s,2H),6.64(dd,J=0.6,2.7Hz,1H),6.79(d,J=8.1Hz,1H),6.90(d,J=8.7Hz,2H),6.96(s,1H),7.02(s,1H),7.19-7.32(m,3H),7.40-7.50(m,3H),7.56-7.60(m,1H),7.85(d,J=0.9Hz,1H),8.58-8.60(m,1H)IR(KBr)3600-2600(br),1611,1599,1500,1477,1445,1395,1264,1238,1210,1052,1029,1008cm-1 |
I-625 | m.p.213-214℃1HNMR(CDCl3)δ2.36(s,3H),3.77(s,6H),6.70(dd,J=0.6,3.6Hz,1H),6.93(s,1H),6.96(s,1H),7.08-7.16(m,2H),7.24-7.28(m,2H),7.51-7.60(m,4H),7.73(d,J=1.5Hz,1H),7.80-7.84(m,2H),8.03(d,J=9.0Hz,1H)IR(KBr)3600-2800(br),1597,1517,1496,1464,1444,1372,1209,1189,1172,1157,1121,1092,1050,1028cm-1 |
I-626 | 1HNMR(CDCl3+CD3OD)δ3.13(s,3H),3.81(s,3H),3.82(s,3H),5.19(s,2H),6.97(s,1H),6.99(s,1H),7.14(d,J=8.7Hz,1H),7.34-7.52(m,6H),7.61(d,J=2.1Hz,1H),7.73(d,J=8.4Hz,2H),8.12(d,J=8.4Hz,2H)IR(KBr)3432,1616,1520,1494,1452,1388,1352,1282,1261,1211,1186,1175,1113,1058,1033cm-1 |
I-627 | 1HNMR(CDCl3)δ3.81(s,6H),5.17(s,2H),6.99(s,1H),7.00(d,J=8.4Hz,1H),7.09(dd,J=8.4&1.8Hz,1H),7.23(d,J=1.8Hz,1H),7.33-7.50(m,5H),7.76(.d,J=8.4Hz,2H),8.10(d,J=8.4Hz,2H)IR(KBr)3551,3520,3399,1615,1587,1576,1521,1488,1455,1383,1268,1245,1208,1126,1055,1034,1003cm-1 |
I-628 | 1HNMR(CDCl3)δ3.05(s,3H),3.47(s,3H),3.75(s,3H),5.15(s,2H),6.45(s,1H),6.94(dd,J=8.4&1.8Hz,1H),7.03(d,J=8.4Hz,1H),7.06(d,J=1.8Hz,1H),7.30(d,J=8.1Hz,2H),7.36-7.51(m,5H),7.63(d,J=8.1Hz,2H)IR(KBr)3525,3472,1609,1588,1522,1487,1455,1407,1321,1286,1242,1148,1115,1071,1013cm-1 |
I-629 | 1HNMR(CDCl3)δ2.68(s,3H),3.07(s,3H),3.14(s,3H),3.55(s,3H),3.78(s,3H),5.19(s,2H),6.85(s,1H),7.16(d,J=8.7Hz,1H),7.27-7.50(m,9H),7.62(d,J=9.0Hz,2H)IR(KBr)3432,1611,1522,1482,1462,1392,1358,1295,1233,1178,1154,1119,1082,1012cm-1 |
I-630 | 1HNMR(CDCl3)δ2.88(s,3H),3.08(s,3H),3.28(s,3H),3.30(s,3H),3.54(s,3H),3.79(s,3H),6.87(s,1H),7.32(d,J=8.4Hz,2H),7.43(d.d,J=8.4&2.1Hz,1H),7.54-7.65(m,4H)IR(KBr)3432,1612,1519,1481,1367,1332,1232,1177,1154,1077,1011cm-1 |
I-631 | 1HNMR(CDCl3)δ1.57(s,3H),1.69(s,3H),2.66(s,3H),2.97(s,3H),3.13(s,3H),3.54(s,3H),3.77(s,3H),4.31(d,J=7.2Hz,2H),5.19(s,2H),5.21-5.32(m,1H),6.86(s,1H),7.15(.d,J=8.7Hz,1H),7.30-7.52(m,9H),7.63(d,J=8.4Hz,2H)IR(KBr)1609,1520,1481,1365,1338,1294,1270,1233,1178,1153,1118,1078,1015,947cm-1 |
I-632 | 1HNMR(CDCl3)δ1.45(s,3H),1.59(s,3H),1.66(s,3H),1.70(s,3H),2.97(s,3H),3.11(s,3H),3.64(s,3H),3.75(s,3H),4.28(d,J=8.4Hz,2H),4.32(d,J=8.4Hz,2H),5.18(s,2H),5.23(t,J=8.4Hz,1H)),5.29(t,J=8 4Hz,1H),6.70(s,1H),7.10(d,J=8.4Hz,1H)7.30-7.51(m,9H),7.58(d,J=8.4Hz,2H) |
I-633 | 1HNMR(CDCl3)δ1.58(s,3H),1.69(s,3H),2.97(s,3H),3.45(s,3H),3.75(s,3H),4.33(d,J=7.5Hz,2H),5.16(s,2H),5.24-5.33(m,1H),5.69(s,1H),5.87(s,1H),6.47(s,1H),6.95(d.d,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.09(.d,J=2.1Hz,1H),7.31-7.50(m,7H),7.65(d,J=8.4Hz,2H)IR(KBr)3450,1609,1590,1558,1524,1487,1448,1421,1320,1233,1143,1117,1073,1019cm-1 |
I-634 | 1HNMR(CDCl3)δ1.57(s,3H),1.68(s,3H),2.66(s,3H),2.70(s,3H),3.13(s,3H),3.54(s,3H),3.78(s,3H),4.33(d,J=8.4Hz,2H),5.19(s,2H),5.26(t,J=8.4Hz),6.86(s,1H),7.15(d,J=8.7Hz,1H),7.30-7.49(m,9H),7.63(d,J=8.4Hz,2H)IR(KBr)1615,1517,1480,1372,1337,1233,1213,1178,1154,1076,1014cm-1 |
I-635 | 1HNMR(CDCl3)δ1.58(s,3H),1.69(s,3H),2.82(s,3H),2.97(s,3H),3.29(s,3H),3.53(s,3H),3.77(s,3H),4.33(d,J=7.2Hz,2H),5.27(t,J=7.2Hz,1H),6.25(s,1H),6.86(s,1H),7.17(d,J=9.0Hz,1H)),7.23-7.32(m,2H),7.41(d,J=8.7Hz,2H),7.63(d,J=8.7Hz,2H)IR(KBr)3431,1611,1522,1482,1364,1337,1294,1231,1178,1153,1077,1014cm-1 |
I-636 | 1HNMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.09(s,3H),3.47(s,3H),3.75(s,3H),4.62(d,J=6.9Hz,2H),5.47-5.58(m,1H),5.71(s,1H),5.87(s,1H),6.45(s,1H),6.60(s,1H),6.89-7.01(m,2H),7.05(d,J=0.6Hz,1H),7.30(.d,J=8.7Hz,2H),7.65(d,J=8.7Hz,2H)IR(KBr)3448,3265,1612,1585,1521,1487,1330,1287,1243,1225,1152,1112,1069,971cm-1 |
I-637 | 1HNM2R(CDCl3)δ1.57(s,3H),1.69(s,3H),1.77(s,3H),1.81(s,3H),2.70(s,3H),2.97(s,3H),3.24(s,3H),3.54(s,3H),3.78(s,3H),4.32(d,J=6.9Hz,2H),4.64(d,J=6.6Hz,2H),5.27(t,J=6.9Hz,1H),5.49(t,J=6.6Hz,1H),6.86(s,1H),7.09(d,J=8.4Hz,1H),7.32-7.44(m,4H),7.63(d,J=8.4Hz,2H)IR(KBr)1609,1520,1481,1365,1339,1292,1270,1236,1178,1153,1118,1078,1015cm-1 |
I-638 | 1HNMR(CDCl3)δ1.58(s,3H),1.69(s,3H),1.76(s,3H),1.82(s,3H),2.97(s,3H),3.45(s,3H),3.75(s,3H),4.32(d,J=7.8Hz,2H),4.63(.d,J=7.8Hz,2H),5.23-5.33(m,1H),5.48-5.57(m,1H),5.69(s,1H),5.85(s,1H),6.46(s,1H),6.89-7.02(m,2H),7.05(d,J=1.8Hz,1H),7.40(d,J=8.7Hz,2H),7.65(d,J=8.7Hz,2H)IR(KBr)3450,1609,1588,1557,1525,1487,1445,1327,1248,1148,1114,1072,1015cm-1 |
I-639 | 1HNMR(CDCl3)δ2.55(s,3H),2.67(s,3H),3.58(s,3H),3.79(s,3H),5.18(s,2H),5.71(s,1H),6.85(s,1H),6.91(d.d,J=8.4&2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.04(d,J=2.1Hz,1H),7.32-7.48(m,6H),.7.85(.d.d,J=7.8&1.5Hz,1H),8.22(d,J=1.5Hz,1H)IR(KBr)3457,1739,1529,1481,1407,1376,1343,1279,1243,1177,1128,1071,1012cm-1 |
I-640 | 1HNMR(CDCl3)δ2.67(s,3H),2.68(s,3H),3.13(s,3H),3.58(s,3H),3.80(s,3H),5.19(s,2H),6.86(s,1H),7.15(d,J=8.7Hz,1H),7.31-7.49(m,8H),7.83(d.d,J=8.1&1.8Hz,1H),8.21(d,J=1.8Hz,1H)IR(KBr)3433,1609,1530,1481,1372,1290,1268,1238,1177,1118,1075,1012cm-1 |
I-641 | 1HNMR(CDCl3)δ2.67(s,3H),3.50(s,3H),3.77(s,3H),5.16(s,2H),5.70(s,1H),5.83(s,1H),6.47(s,1H),6.94(d.d,J=8.7&1.8Hz,1H),7.04(d,J=8.7Hz,1H),7.07(d,J=1.8Hz,1H),7.34-7.48(m,5H),7.82(d.d,J=8.1&1.8Hz,1H),8.26(d,J=1.8Hz,1H)IR(KBr)3555,3377,1590,1529,1503,1451,1414,1341,1324,1242,1225,1121cm-1 |
I-642 | 1HNMR(CDCl3)δ2.29(s,3H),2.68(s,3H),3.12(s,3H),3.56(s,3H),3.76(s,3H),5.18(s,2H),6.85(s,1H),7.00-7.20(m,4H),7.31-7.49(m,7H)IR(KBr)3407,1624,1518,1480,1361,1287,1270,1234,1175,1117,1084,1009cm-1 |
I-643 | 1HNMR(CDCl3)δ2.40(s,3H),2.67(s,3H),3.09(s,3H),3.13(s,3H),3.59(s,3H),3.78(s,3H),5.19(s,1H),6.17(s,1H),6.85(s,1H),7.15(d,J=8.4Hz,1H),7.30-7.49(m,9H),7.69(d,J=1.8Hz,1H)IR(KBr)3433,3304,1608,1519,1481,1365,1326,1294,1269,1237,1177,1156,1114,1079,1015cm-1 |
I-644 | 1HNMR(CDCl3)δ2.09(s,3H),2.39(s,3H),2.68(s,3H),3.13(s,3H),3.49(s,3H),3.76(s,2H),5.19(s,2H),6.30(s,1H),6.77(s,1H),7.12-7.24(m,3H),7.31-7.49(m,9H),7.54(d,J=1.8Hz,1H),7.67(d,J=8.4Hz,2H)IR(KBr)3434,1608,1519,1481,1366,1293,1269,1237,1164,1114,1081,1016cm-1 |
I-645 | 1HNMR(CDCl3)δ2.09(s,3H),2.39(s,3H),3.43(s,3H),3.73(s,3H),5.16(s,2H),5.30(s,1H),5.68(s,1H),5.89(s,1H),6.32(s,1H),6.36(s,1H),6.95(d.d,J=8.7&2.1Hz,1H),7.03(d,J=8.7Hz,1H),7.08(d,J=2.1Hz,1H),7.14-7.28(m,3H),7.34-7.50(m,5H),7.61(d,J=1.5Hz,1H),7.68(d,J=8.4Hz,2H)IR(KBr)3465,3270 1612,1587,1558,1519,1487,1454,1384,1244,1160,1123,1105,1091,1070,1009cm-1 |
I-646 | 1HNMR(CDCl3)δ2.48(s,3H),2.63(s,3H),3.02(s,3H),3.13(s,3H),3.28(s,2H),3.54(s,3H),3.78(s,3H),5.19(s,2H),6.85(s,1H),7.15(d,J=8.4Hz,1H),7.30-7.49(m,9H),7.59(s,1H)IR(KBr)3433,1606,1519,1481,1364,1341,1292,1272,1233,1178,1148,1118,1082cm-1 |
I-647 | 1HNMR(CDCl3)δ2.48(s,3H),3.02(s,3H),3.28(s,3H),3.46(s,3H),3.75(s,3H),5.16(s,2H),5.70(s,1H),5.84(s,1H),6.47(s,1H),6.94(d.d,J=8.4&2.1Hz,1H),7.03(.d,J=8.4Hz,1H),7.07(d,J=2.1Hz,1H),7.33-7.53(m,7H),7.62(d,J=1.8Hz,1H)IR(KBr)3528,3429,1609,1584,1558,1517,1487,1454,1331,1317,1137,1115,1068,1002cm-1 |
I-648 | 1HNMR(CDCl3)δ1.55(s,3H),2.45(s,3H),2.79(s,3H),3.02(s,3H),3.29(s,3H),3.52(s,3H),3.77(s,3H),4.12-4.31(m,2H),5.22-5.31(m,1H),6.30(s,11H),6.84(s,1H),7.17(d,J=8.7Hz,1H),7.25-7.32(m,2H),7.39(d,J=8.4Hz,1H),7.45(d.d,J=8.4&1.8Hz,1H),7.53(d,J=1.8Hz,1H)IR(KBr)3431,1609,1522,1481,1365,1334,1294,1235,1178,1150,1077,1013cm-1 |
I-649 | 1HNMR(CDCl3)δ1.54(s,3H),1.68(s,3H),1.76(s,3H),1.81(s,3H),2.45(s,3H),2.68(s,3H),3.02(s,3H),3.24(s,3H),3.52(s,3H),3.78(s,3H),4.10.4.34(m,2H),4.64(d,J=7.2Hz,2H),5.21-5.30(m,1H),5.45-5.53(m,1H),6.84(s,1H),7.08(d,J=8.4Hz,1H),7.31-7.48(m,4H),7.53(d,J=1.5Hz,1H)IR(KBr)3432,1606,1518,1481,1362,1340,1292,1276,1236,1177,1153,1116,1076,1010cm-1 |
I-650 | 1HNMR(CDCl3)δ1.56(s,3H),1.68(s,3H),1.76(s,3H),1.82(s,3H),2.44(s,3H),3.02(s,3H),3.45(s,3H),3.75(s,3H),4.10-4.32(m,2H),4.62(d,J=7.2Hz,2H),5.22-5.32(m,1H),5.48-5.57(m,1H),5.60-5.80(brroad,1H),5.82(s,1H),6.46(s,1H),6.92(d.d,J=8.1&1.8Hz,1H),6.97(d,J=8.1Hz,1H),7.04(d,J=1.8Hz,1H),7.38(d,J=8.1Hz,1H),7.47(d.d,J=8.1&1.8Hz,1H),7.57(d,J=1.8Hz,1H)IR(KBr)3433,1610,1586,1557,1518,1486,1336,1240,1149,1110,1069cm-1 |
I-651 | 1HNMR(CD3OD)δ3.33(s,3H),3.66(s,3H),5.18(s,2H),6.42(s,1H),1H),6.75(dd,J=8.4&2.1Hz,1H),6.87(d,J=2.1Hz,1H),6.95(d,J=8.4Hz,1H),7.26-7.58(m,8H),7.81(d.d,J=7.8&1.2Hz,1H)IR(KBr)3446,1698,1586,1517,1498,1481,1454,1408,1287,1247,1117,1069,1010cm-1 |
I-652 | 1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.76(s,3H),3.23(s,3H),3.43(s,3H),3.72(s,3H),3.76(s,3H),4.64(d,J=6,6Hz,2H),5.50(t,J=6.6Hz,1H),6.78(s,1H),7.08(d,J=8.7Hz,1H),7.33-7.51(m,4H),7.56-7.63(m,1H),7.96(d.d,J=7.5&1.2Hz,1H)IR(KBr)1725,1609,1520,1480,1400,1366,1295,1260,1178,1119,1073,1010cm-1 |
I-653 | 1HNMR(CDCl3)δ2.38(s,3H),2.72(s,3H),3.12(s,3H),3.43(s,3H),3.73(s,3H),3.76(s,3H),5.14(s,2H),6.79(s,1H),7.13-7.24(m,3H),7.30-7.38(m,3H),7.41-7.51(m,3H),7.56-7.63(m,1H),795(d.d,J=7.5&1.2Hz,1H)IR(KBr)1725,1610,1520,1481,1401,1370,1293,1262,1179,1119,1076,1011cm-1 |
I-654 | 1HNMR(CDCl3)δ1.75(s,3H),1.81(s,3H),3.56(s,3H),3.72(s,3H),4.60(d,J=6.6Hz,2H),5.29(s,1H),5.46-5.56(m,1H),5.56-6.00(brond,1H),6.42(s,1H),6.94(s,2H),7.05(s,1H),7.43-7.52(m,2H),7.56-7.65(m,1H),7.99(.d,J=8.7Hz,1H)IR(KBr)3433,1697,1585,1517,1481,1454,1410,1287,1244,1117,1068cm-1 |
I-655 | 1HNMR(CDCl3)δ2.39(s,3H),3.37(s,3H),3.72(s,3H),5.10(s,2H),6.41(s,1H),6.94(dd,J=8.1&2.1Hz,1H),7.02(d,J=8.1Hz,1H),7.06(d,J=2.1Hz,1H),7.23(d,J=7.8Hz,2H),7.35(.d,J=7.8Hz,2H),7.42-7.63(m,3H),7.96(d,J=7.8Hz,1H)IR(KBr)3538,3443,1685,1518,1458,1413,1253,1116,1069,1010cm-1 |
I-656 | m.p.110-112℃1HNMR(CDCl3)δ1.69(s,3H),1.74(s,3H),2.55(q,J=7.1Hz,2H),3.20(s,3H),3.21(s,3H),3.39(s,3H),3.70(s,3H),4.07(t,J=7.1Hz,2H),5.22(t,J=7.1Hz,1H),6.28(s,1H),7.09(d,J=8.4Hz,1H),7.32(dd,J=8.4,2.0Hz,1H),7.36(d,J=8.9Hz,2H),7.37(d,J=2.0Hz,1H),7.69(d,J=8.9Hz,2H)IR(KBr)3477,3402,1607,1518,1481,1365,1151,1111,872,813cm-1 |
I-657 | m.p.159-162℃1HNMR(DMSO-d6)δ1.64(s,3H),1.71(s,3H),2.45(q,J=6.7Hz,2H),3.27(s,3H),3.59(s,3H),3.96(t,J=6.7Hz,2H),4.22(s,2H),5.26(t,J=6.7Hz,1H),6.17(s,1H),6.60(dd,J=8.1,2.0Hz,1H),6.67(d,J=2.0Hz,1H),6.83(d,J=8.7Hz,2H),6.95(d,J=8.Hz,1H),7.42(d,J=8.7Hz,2H),8.89(s,1H),9.46(s,1H)IR(KBr)3447,3401,3361,1611,1522,1486,1260,1228,1122,1001,814cm-1 |
I-658 | m.p.146-147℃1HNMR(CDCl3)δ1.14(t,J=7.2Hz,3H),1.76(d,J=0.9Hz,3H),1.81(d,J=0.3Hz,3H),2.70(s,3H),3.20(s,3H),3.23(s,3H),3.72(q,J=7.2Hz,2H),3.78(s,3H),4.64(d,J=6.6Hz,2H),5.49(m,1H),6.84(s,1H),7.09(d,J=8.4Hz,1H),7.31-7.41(m,4H),7.66-7.74(m,2H)IR(CHCl3)2930,1608,1517,1479,1369,1148,1116,1082,969,872cm-1 |
I-659 | m.p.174-175℃1HNMR(CDCl3)δ1.14(t,J=6.9Hz,3H),2.37(s,3H),2.65(s,3H),3.12(s,3H),3.20(s,3H),3.72(q,J=6.9Hz,2H),3.77(s,3H),5.14(s,2H),6.84(s,1H),7.15(d,J=8.4Hz,1H),7.18-7.42(m,6H),7.66-7.73(m,2H)IR(CHCl3)1517,1479,1369,1268,1148-1117,1082,969,872cm-1 |
I-660 | m.p.147.5-148℃1HNMR(CDCl3)δ1.14(t,J=7.2Hz,3H),1.68(s,3H),1.74(d,J=0.9Hz,3H),2.50-2.59(m,2H),2.72(s,3H),3.20(s,3H),3.22(s,3H),3.72(q,J=7.2Hz,2H),3.77(s,3H),4.07(d,J=6.9Hz,2H),5.21(m,1H),6.84(s,1H),7.07(d,J=8.7Hz,1H),7.31-7.42(m,4H),7.66-7.74(m,2H)IR(CHCl3)2930,1607,1517,1480,1369,1148,1118,1082,1025,969,872cm-1 |
I-661 | m.p.154-157℃1HNMR(CDCl3)δ1.15(t,J=7.2Hz,3H),1.76(s,3H),1.82(s,3H),3.60(q,J=7.2Hz,2H),3.75(s,3H),4.61(d,J=6.9Hz,2H),4.93(s,1H),5.53(m,1H),5.69(s,1H),5.96(s,1H),6.45(s,1H),6.80-6.98(m,4H),7.07(m,1H),7.51-7.58(m,2H)IR(CHCl3)3592,3528,2976,2934,1611,1521,1488,1460,1384,1286,1243,1169,1112,1068,994,885,824cm-1 |
I-662 | m.p.130.5-133℃1HNMR(CDCl3)δ1.15(t,J=7.2Hz,3H),2.39(s,3H),3.59(q,J=7.2Hz,2H),3.74(s,3H),4.s3(s,1H),5.10(s,2H),5.66(s,1H),5.97(s,1H),6.44(s,1H),6.87-6.94(m,2H),6.96(dd,J=1.8,8.4Hz,1H),7.02(d,J=8.4Hz,1H),7.09(d,J=1.8Hz,1H),7.19-7.26(m,2H),7.30-7.38(m,2H),7.51-7.58(m,2H)IR(CHCl3)3524,1612,1521,1488,1460,1383,1286,1246,1113,1069,1027,907,873cm-1 |
I-663 | 无定形粉末1HNMR(CDCl3)δ1.15(t,J=7.2Hz,3H),1.68(d,J=0.6Hz,3H),1.74(d,J=0.9Hz,3H),2.48-2.56(m,2H),3.60(q,J=7.2Hz,2H),3.74(s,3H),4.06(d,J=6.9Hz,2H),4.95(s,1H),5.22(m,1H),5.68(s,1H),5.96(s,1H),6.44(s,1H),6.88-6.99(m,4H),7.06(d,J=1.2Hz,1H),7.51-7.58(m,2H)IR(CHCl3)3528,2972,1611,1521,1488,1384,1286,1246,1112,1068,1024,883,824cm-1 |
I-664 | m.p.113-116℃1HNMR(CDCl3)δ2.55(s,6H),3.45(s,3H),3.74(s,3H),5.31(s,2H),6.44(s,1H),6.92(d,J=8.7Hz,2H),6.94(dd,J=8.4,2.1Hz,1H),7.10(s,1H),7.10(d,J=2.1Hz,1H),7.20(d,J=8.7Hz,1H),7.52(d,J=8.7Hz,2H)IR(Nujol)3491,3443,3304,3155,1662,1608,1523,1492,1464,1251,1215,1111,1067,811,782cm-1 |
I-665 | m.p.>260℃1HNMR(CD3OD)δ3.39(s,3H),3.66(s,3H),5.40(s,2H),6.44(s,1H),6.83(dd,J=8.4,2.1Hz,1H),6.85(d,J=8.7,2H),6.90(d,J=2.1Hz,1H),7.11(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3350,2668,1611,1595,1530,1488,1458,1402,1253,1213,1116,1073,1016,837,817,781cm-1 |
I-666 | 泡沫1HNMR(CDCl3)δ2.34(s,3H),2.44(s,3H),2.83(s,3H),3.12(s,3H),3.22(s,3H),3.55(s,3H),3.78(s,3H),4.92(s,2H),6.85(s,1H),7.17(d,J=8.4Hz,1H),7.37~7.42(m,2H),7.39(d,J=8.7Hz,2H),7.68(d,J=8.7Hz,2H)IR(Nujol)1638,1608,1519,1480,1459,1177,1151,1079,971,876,844,798cm-1 |
I-667 | 泡沫1HNMR(CDCl3)δ2.07(s,3H),2.53(s,3H),2.96(s,3H),3.23(s,3H),3.27(s,3H),3.54(s,3H),3.78(s,3H),4.86(s,2H),6.86(s,1H),7.11(d,J=9.0Hz,1H),7.33~7.41(m,2H),7.39(d,J=8.7Hz,2H),7.67(d,J=8.7Hz,2H)IR(Nujol)1724,1688,1610,1520,1481,1464,1234,1177,1151,1123,1081,876,798cm-1 |
I-668 | m.p.221-223℃1HNMR(DMSO-d6)δ3.30(s,3H),3.64(s,3H),5.16(s,2H),6.39(s,1H),6.66(dd,J=8.4,2.1Hz,1H),6.77(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),7.00(d,J=8.4Hz,1H),7.34(s,1H),7.44(d,J=8.7Hz,2H),8.43(s,1H)IR(Nujol)3535,3411,1611,1582,1521,1488,1463,1244,1194,1135,1119,1074,1014,930,826,809cm-1 |
I-669 | 泡沫1HNMR(CDCl3)δ2.79(s,3H),3.17(s,3H),3.22(s,3H),3.55(s,3H),3.78(s,3H),5.21(s,2H),6.85(s,1H),7.19(d,J=8.4Hz,1H),7.23(s,1H),7.38(dd,J=8.7,2.1Hz,1H),7.39(d,J=8.7Hz,2H),7.42(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H),7.94(s,1H)IR(Nujol)1608,1519,1480,1463,1177,1151,1119,1079,971,876,798cm-1 |
I-670 | m.p.198-201℃1HNMR(DMSO-d6)δ2.88(s,3H),3.39(s,3H),3.45(s,3H),3.52(s,3H),3.78(s,3H),4.58(s,2H),5.60(s,1H),7.07(s,1H),7.29(dd,J=9.0,1.8Hz,1H),7.30(d,J=1.8Hz,1H),7.37(d,J=9.0Hz,1H),7.48(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H),9.39(s,1H)IR(Nujol)3576,3500,3405,3391,1668,1607,1590,1520,1480,1462,1175,1156,1081,1014,880,836,826,801cm-1 |
1-671 | 泡沫1HNMR(CDCl3)δ2.61(s,3H),2.73(s,3H),3.21(s,3H),3.23(s,3H),3.55(s,3H),3.78(s,3H),5.32(s,2H),6.84(s,1H),7.17(d,J=8.4Hz,1H),7.36(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7,Hz,2H),7.43(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H),8.46(s,1H),8.75(s,1H)IR(Nujol)1608,1519,1481,1463,1177,1151,1080,971,876,798cm-1 |
I-672 | 泡沫1HNMR(CDCl3)δ2.75(s,3H),3.21(s,3H),3.25(s,3H),3.55(s,3H),3.78(s,3H),5.37(s,2H),6.84(s,1H),7.17(d,J=8.4Hz,1H),7.36(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7,Hz,2H),7.43(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H),8.59(s,1H),8.92(s,1H)IR(Nujol)1608,1519,1480,1463,1177,1151,1080,971,876,798cm-1 |
I-673 | 泡沫1HNMR(CDCl3)δ2.70(s,3H),3.15(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.14(s,2H),6.77(m,2H),6.84(s,1H),7.19(m,2H),7.26(d,J=8.4Hz,1H),7.37(d,J=2.1Hz,1H),7.38(dd,J=2.1,8.4Hz,1H),7.68(d,J=8.4Hz,2H) |
I-674 | m.p.153-156℃1HNMR(CDCl3)δ2.18(s,3H),2.81(s,3H),3.18(s,3H),3.22(s,3H),3.55(s,3H),3.79(s,3H),5.14(s,2H),6.86(s,1H),7.18(dd,J=8.1,8.1Hz,1H),7.24(d,J=8.1Hz,1H),7.26(d,J=8.4Hz,1H),7.36(d,J=1.8Hz,1H),7.38(d,J=8.4Hz,2H),7.39(dd,J=1.8,8.4Hz,1H),7.43(dd,J=8.1,8.1Hz,1H),7.67(d,J=8.4Hz,2H),7.90(d,J=8.1Hz,1H)IR(KBr)3384,1689,1519,1481,1364,1177,1151,1079,970,874,798cm-1 |
I-675 | 泡沫1HNMR(CDCl3)δ2.76(s,3H),3.16(s,3H),3.22(s,3H),3.23(s,3H),3.55(s,3H),3.78(s,3H),5.23(s,2H),6.85(s,1H),7.23(dd,J=7.5,7.5Hz,1H),7.37(s,2H),7.38(d,J=8.4Hz,2H),7.43(m,3H),7.54(d,J=7.5Hz,1H),7.68(d,J=8.4Hz,2H)IR(KBr)3435,1609,1519,1481,1364,1177,1152,1079,972,876,798cm-1 |
I-676 | m.p.163-165℃1HNMR(CDCl3)δ2.78(s,3H),3.03(s,3H),3.21(s,3H),3.45(s,6H),3.55(s,3H),3.79(s,3H),5.31(s,2H),6.84(s,1H),7.22(d,J=8.4Hz,1H),7.37(dd,J=2.4,8.4Hz,1H),7.38(d,J=8.4Hz,2H),7.42(m,2H),7.53(m,2H),7.67(d,J=8.4Hz,2H),7.68(m,1H)IR(KBr)1609,1519,1481,1365,1176,1161,1080,973,875,799cm-1 |
I-677 | m.p.153-156℃1HNMR(CDCl3)δ2.69(s,3H),2.98(s,3H),3.17(s,3H),3.21(s,3H),3.33(s,3H),3.56(s,3H),3.78(s,3H),5.44(s,2H),6.84(s,1H),7.21(d,J=8.7Hz,1H),7.31-7.46(m,5H),7.38(d,J=8.4Hz,2H),7.68(d,J=8.4Hz,2H),7.72(m,1H)IR(KBr)1610,1519,1481,1365,1177,1149,1079,963,876,799cm-1 |
I-678 | 泡沫1HNMR(CDCl3)δ2.60(s,3H),2.75(s,6H),3.17(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.31(s,2H),6.83(s,1H),7.08(dd,J=7.5,7.5Hz,1H),7.16(d,J=8.4Hz,1H),7.17(d,J=7.5Hz,1H),7.30(dd,J=2.1,8.4Hz,1H),7.32(dd,J=7.5,7.5Hz,1H),7.37(d,J=8.4Hz,2H),7.38(d,J=2.1Hz,1H),7.52(d,J=7.5Hz,1H),7.68(d,J=8.4Hz,2H)IR(KBr)1609,1519,1480,1365,1235,1177,1151,1079,970,874,797cm-1 |
I-679 | m.p.95-97℃1HNMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.03(s,3H),3.21(s,3H),3.56(s,3H),3.75(s,3H),4.63(d,J=6.9Hz,2H),4.93(s,2H),5.51(m,1H),6.66(s,1H),7.05(d,J=8.4Hz,1H),7.09-7.17(m,2H),7.37(dd,J=2.4,8.4Hz,1H),7.44(d,J=2.4Hz,1H),7.51-7.58(m,2H)IR(KBr)3435,2936,1605,1519,1475,1382,1365,1232,1161,1109,1080cm-1 |
I-680 | m.p.142-144℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.07(s,3H),3.57(s,3H),3.74(s,3H),4.61(d,J=6.6Hz,2H),4.90(s,2H),5.51(m,1H),5.65(s,1H),6.66(s,1H),6.92(m,2H),7.03(m,1H),7.09-7.17(m,2H),7.52-7.58(m,2H)IR(KBr)3455,2964,2932,1606,1583,1519,1479,1387,1283,1227,1153,1115,1080,1094,1004cm-1 |
I-681 | m.p.158-160℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.20(s,3H),3.42(s,3H),3.76(s,3H),4.63(d,J=6.6Hz,2H),5.51(m,1H),6.04(s,1H),6.43(s,1H),7.07(d,J=8.4Hz,1H),7.11-7.19(m,2H),7.42(dd,J=2.1,8.4Hz,1H),7.50(d,J=2.1Hz,1H),7.58-7.65(m,2H)IR(KBr)3505,3440,1613,1522,1489,1386,1352,1292,1227.1109,1013cm-1 |
I-682 | m.p.175-178℃1HNMR(CDCl3)δ1.63(s,3H),1.92-2.13(m,4H),3.22(s,3H),3.42(s,3H),3.76(s,3H),4.13(t,J=6.3Hz,2H),6.04(s,1H),6.44(s,1H),7.06(d,J=8.4Hz,1H),7.11-7.19(m,2H),7.43(dd,J=2.1,8.4Hz,1H),7.49(d,J=2.1Hz,1H),7.57-7.65(m,2H)IR(KBr)3467,2973,2943,1613,1523,1489,1359,1232,1113,1072cm-1 |
I-683 | 粉末1HNMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.48-2.57(m,2H),3.08(s,3H),3.57(s,3H),3.74(s,3H),4.06(t,J=6.9Hz,2H),4.90(s,2H),5.22(m,1H),5.64(s,1H),6.66(s,1H),6.91(m,2H),7.03(m,1H),7.08-7.17(m,2H),7.52-7.59(m,2H)IR(KBr)3432,2930,1604,1583,1518,1475,1382,1280,1249,1222,1160,1111,1082cm-1 |
I-684 | m.p.151-153℃1HNMR(CDCl3)δ1.69(s,3H),1.73(s,3H),2.50.2.59(m,2H),3.19(s,3H),3.42(s,3H),3.76(s,3H),4.06(t,J=6.9Hz,2H),5.21(m,1H),6.02(s,1H),6.43(s,1H),7.05(d,J=8.4Hz,1H),7.11-7.19(m,2H),7.42(dd,J=2.4,8.4Hz,1H),7.50(d,J=2.4Hz,1H),7.57-7.65(m,2H)IR(KBr)3457,2937,1613,1523,1489,1465,1390,1361,1295,1234,1185,1110,1072,1013cm-1 |
I-685 | m.p.156-158℃1HNMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.21(s,3H),3.42(s,3H),3.76(s,3H),4.54(d,J=6,9Hz,2H),5.52(t,J=6.9Hz,1H),6.94(s,1H),6.94(d,J=8.7Hz,2H),7.29(d,J=8.7Hz,2H),7.37(d,J=8.7Hz,2H),7.71(d,J=8.7Hz,2H)IR(KBr)1734,1517,1464,1360,1237,1150,1061,988,862cm-1 |
I-686 | m.p.189-191℃1HNMR(CDCl3)δ3.21(s,3H),3.21(s,3H),3.42(s,3H),3.61(s,3H),3.76(s,3H),5.09(s,2H),6.94(s,1H),7.10(d,J=8.4Hz,2H),7.28-7.48(m,9H),7.71(d,J=8.4Hz,2H)IR(KBr)1727,1518,1469,1365,1239,1152,1061,865cm-1 |
I-687 | m.p.112-113℃1HNMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.50(q,J=7.2Hz,2H),3.21(s,3H),3.42(s,3H),3.62(s,3H),3.76(s,3H),3.96(t,J=7.2Hz,2H),5.23(t,J=7.2Hz,1H),6.92(d,J=8.8Hz,2H),6.93(s,1H),7.28(d,J=8.8Hz,2H),7.37(d,J=8.8Hz,2H),7.71(d,J=8.8Hz,2H)IR(KBr)1735,1519,1469,1361,1246,1153,1059,877,861,847,791cm-1 |
I-688 | m.p.191-193℃1HNMR(DMSO-d6)δ1.73(s,3H),1.76(s,3H),3.31(s,3H),3.71(s,3H),4.54(d,J=6.9Hz,2H),5.46(t,J=6.9Hz,1H),(s,1H),6.87(d,J=8.7Hz,2H),6.91(s,1H),6.92(d,J=8.7Hz,2H),7.19(d,J=8.7Hz,2H),7.48(d,J=8.7Hz,2H),9.59(s,1H),12.8(brs,1H)IR(KBr)3462,1695,1609,1520,1472,1231,1177,1062,1001,837cm-1 |
I-689 | m.p.229-232℃1HNM R(DMSO-d6)δ3.31(s,3H),3.71(s,3H),5.12(s,2H),6.87(d,J=8.8Hz,2H),6.98(s,1H),7.01(d,J=8.8Hz,2H),7.21(d,J=8.8Hz,2H),7.34-7.50(m,7H),9.58(s,1H),12.8(brs,1H)IR(KBr)3424,3238,1685,1610,1521,1464,1379,1235,1180,1057,1001,826cm-1 |
I-690 | m.p.171-172℃1HNMR(DMSO-d6)δ1.64(s,3H),1.70(s,3H),2.43(q,J=6.9Hz,2H),3.31(s,3H),3.70(s,3H),3.96(t,J=6.9Hz,2H),5.23(t,J=6.9Hz,1H),6.87(d,J=8.8Hz,2H),6.91(d,J=8.8Hz,2H),6.98(s,1H),7.19(d,J=8.8Hz,2H),7.48(d,J=8.8Hz,2H),9.58(s,1H),12.8(brs,1H)IR(KBr)3402,3266,1689,1612,1521,1470,1376,1241,1181,1063,1001,829cm-1 |
I-691 | mp191-193℃1HNMR(CDCl3)δ2.55(s,3H),3.52(s,3H),3.77(s,3H),5.17(s,2H),5.70(s,1H),6.83(s,1H),6.91(dd,J=1.8,8.1Hz,1H),7.00-7.05(m,2H),7.10-7.19(m,2H),7.34-7.45(m,5H),7.57-7.65(m,2H)IR(KBr)3030,2934,1606,1523,1487,1391,1358,1290,1228,1077,1019,947,831,815,803cm-1 |
I-692 | mp172-173℃1HNMR(CDCl3)δ2.47(s,3H),3.52(s,3H),3.53(s,3H),3.77(s,3H),5.21(s,2H),5.25(s,2H),6.82(s,1H),7.01-7.03(m,2H),7.11-7.18(m,2H),7.22-7.41(m,6H),7.57-7.63(m,2H)IR(KBr)3010,2931,1602,1519,1484,1385,1369,1232,1174,1085,847,806,729,527cm-1 |
I-693 | mp129-132℃1HNMR(CDCl3)δ3.44(s,3H),3.53(s,3H),3.75(s,3H),5.20(s,2H),5.26(s,2H),5.91(s,1H),6.44(s,1H),7.01(d,J=8.1Hz,1H),7.08(dd,J=1.8Hz,8.1Hz,1H),7.11-7.18(m,2H),7.28-7.50(m,6H),7.57-7.64(m,2H)IR(KBr)2996,2952,2932,2895,1609,1522,1488,1229,1120,1075,999,911,815,724,582cm-1 |
I-694 | mp124-126℃1HNMR(CDCl8)δ1.76(d,J=0.6Hz,3H),1.80(d,J=0.9Hz,3H),2.69(2H,s),3.54(s,3H),3.57(s,3H),3.76(s,3H),4.64(d,J=6.6Hz,2H),5.26(s,3H),5.54(m,1H),6.86(s,1H),6.98(d,J=8.7Hz,1H),7.13-7.25(m,3H),7.38-7.43(m,3H)IR(CHCl3)2935,2855,1675,1603,1520,1481,1387,1370,1247,1178,1158,1134,1081,1003,961,839,814cm-1 |
I-695 | mp141-142℃1HNMR(CDCl3)δ2.34(s,3H),2.48(s,3H),5.16(s,2H),5.70(s,1H),6.82(dd,J=8.4,2.1Hz,1H),6.97-7.00(m,2H),7.07-7.13(m,4H),7.32-7.46(m,7H)IR(CHCl3)3543,3023,2871,1604,1587,1520,1489,1469,1383,1267,1243,1158,1126,1014,957,877,839cm-1 |
I-696 | mp178-180℃1HNMR(CDCl3)δ2.75(s,3H),3.18(s,3H),3.55(s,3H),3.76(s,3H),5.18(s,2H),5.72(s,1H),6.87(s,1H),7.00(d,J=8.7Hz,1H),7.15(dd,J=8.7,2.1Hz,1H),7.24-7.28(m,21H),7.36-7.50(m,8H)IR(CHCl3)3543,3027,2939,1519,1481,1371,1330,1254,1204,1177,1150,1082,1005,969,873cm-1 |
I-697 | mp129-130℃1HNMR(CDCl3)δ2.24(s,3H),2.29(s,3H),3.12(s,3H),5.18(s,2H),7.08-7.14(m,5H),7.25-7.50(m,9H)IR(CHCl3)2925,2871,1604,1520,1490,1455,1369,1291,1262,1169,1111,1007,972,957,882,840,816cm-1 |
I-698 | mp124-125℃1HNMR(CDCl3)δ1.77(s,3H),1.81-1.82(d,J=0.9Hz,3H),2.24(s,3H),2.28(s,3H),3.22(s,3H),4.63(d,J=6.6Hz,2H),5.52(m,1H),7.04-7.14(m,5H),7.24-7.34(m,4H)IR(KBr)2978,2924,2868,1893,1771,1604,1520,1489,1368,1290,1261,1169,1109,1046,973,957,882,740,816cm-1 |
I-699 | 油状物1HNMR(CDCl3)δ1.69(s,3H),1.74-1.75(d,J=0.9Hz,3H),2.24(s,3H),2.28(s,3H),2.55(m,2H),3.21(s,3H),4.05-4.10(t,J=6.9Hz,2H),5.22(m,1H),7.03-7.14(m,5H),7.24-7.34(m,4H)IR(CHCl3)2970,2926,2875,1605,1520,1490,1470,1368,1292,1277,1169,1110,1016,973,958,878,840,819cm-1 |
I-700 | mp121-123℃1HNMR(CDCl3)δ2.24(s,3H),2.83(s,3H),2.98(s,3H),3.11(s,3H),5.13(s,2H),7.08-7.14(m,4H),7.21-7.37(m,9H)RR(CHCl3)2925,1605,1520,1489,1369,1262,1169,1014,1003,972,957,882,840,816cm-1 |
I-701 | mp215-217℃1H NMR(CDCl3)δ2.73(s,3H),3.13(s,3H),3.18(s,3H),3.57(s,3H),3.78(s,3H),5.20(s,2H),6.86(s,1H),7.16(d,J=8.7Hz,1H),7.35-7.50(m,9H),7.56(dd,J=8.4,2.4Hz,1H),7.62(d,J=2.4Hz,1H)IR(CHCl3)2939,1613,1519,1480,1371,1294,1254,1176,1150,1119,1083,1003,970,871,849,816cm-1 |
I-702 | mp71-73℃1H NMR(CDCl3)δ1.77(s,3H),1.83(s,3H),2.24(s,3H),2.29(s,3H),4.61-4.64(d,J=6.9Hz,2H),5.54(m,1H),5.71(s,1H),6.80-6.84(dd,J=8.4,2.1Hz,1H),6.92(d,J=8.4Hz,1H),7.07-7.13(m,4H),7.30-7.35(m,2H)IR(KBr)3537,2977,2924,2868,1604,1585,1520,1489,1450,1386,1292,1267,1242,1158,1125,996,957,839cm-1 |
1-703 | 油状物1H NMR(CDCl3)δ1.69(s,3H),1.75-1.76(d,J=0.9Hz,3H),2.24(s,3H),2.28(s,3H),2.50-2.57(td,J=6.9,6.3Hz,2H),4.05-4.10(t,J=6.3Hz,2H),5.24(m,1H),5.70(s,1H),6.81(dd,J=8.4,1.8Hz,1H),6.90(d,J=8.4Hz,1H),6.96(d,J=1.8Hz,1H),7.06-7.13(m,4H),7.26-7.34(m,2H)IR(CHCl3) 3540,2972,2925,2877,1604,1585,1520,1490,1387,1293,1267,1245,1158,1127,1016,957,839cm-1 |
I-704 | mp113-115℃1H NMR(CDCl3)δ2.24(s,3H),2.28(s,3H),2.39(s,3H),5.11(s,2H),5.69(s,1H),6.82(dd,J=8.4,2.4Hz,1H),6.97-7.00(m,2H),7.07-7.13(m,3H),7.22-7.36(m,7H)IR(CHCl3)3541,2925,2871,1604,1586,1520,1490,1469,1380,1324,1308,1292,1267,1243,1201,1158,1126,1013,957,876,839cm-1 |
I-705 | 泡沫1H NMR(CDCl3)δ3.20(s,3H),3.27(s,3H),3.43(s,3H),3.73(s,3H),4.37(br d,J=5.7Hz,2H),4.58(s,2H),5.16(s,2H),5.68(s,1H),6.82(dd,J=8.2,1.7Hz,1H),6.88(s,1H),6.97(d,J=1.7Hz,1H),6.98(d,J=8.2Hz,1H),7.35-7.47(m,7H),7.71(d,J=8.7Hz,2H)IR(KBr)3464,1515,1474,1369,1230,1199,1176,1149,1039,873cm-1 |
I-706 | 泡沫1H NMR(CDCl3)δ2.42(br s,1H),3.12(s,3H),3.22(s,3H),3.45(s,3H),3.74(s,3H),4.49(br s,1H),5.18(s,2H),6.85(s,1H),7.15(d,J=8.6Hz,1H),7.27(dd,J=8.6,2.0Hz,1H),7.35.7.50(m,8H),7.71(d,J=8.6Hz,2H)IR(KBr)3583,3435,1519,1467,1412,1229,1180,1150,1022,875,849,798,742,706cm-1 |
I-707 | mp120-121℃1H NMR(CDCl3)δ3.45(s,3H),3.45(s,3H),3.75(s,3H),4.66(s,2H),4.77(s,2H),5.15(s,2H),5-67(s,1H),5.91(s,1H),6.47(s,1H),6.96(dd,J=8.4,1.9Hz,1H),7.03(d,J=8.4Hz,1H),7.09(d,J=1.9Hz,1H),7.37-7.47(m,7H),7.64(d,J=8.4Hz,2H)IR(KBr)3504,3461,1522,1485,1466,1384,1466,1384,1283,1245,1197,1110,1042,925,812,749cm-1 |
I-708 | mp156-158℃1H NMR(CDCl3)δ3.11(s,3H),3.21(s,3H),3.28(s,3H),3.42(s,3H),3.73(s,3H),4.38(s,2H),4.58(s,2H),5.18(s,2H),6.88(s,1H),7.12(d,J=8.7Hz,1H),7.27(dd,J=8.7,2.1Hz,1H),7.35-7.50(m,8H),7.70(d,J=8.7Hz,2H)IR(KBr)1514,1469,1360,1177,1149,1099,1042,870cm-1 |
I-709 | mp188-190℃1H NMR(CDCl3)δ1.70(t,J=5.7Hz,1H),3.45(s,3H),3.75(s,3H),4.77(d,J=5.7Hz,2H),5.16(s,2H),5.68(s,1H),5.91(s,1H),6.47(s,1H),6.96(dd,J=8.5,1.7Hz,1H),7.03(d,J=8.5Hz,1H),7.09(d,J=1.7Hz,1H),7.37-7.48(m,7H),7.65(d,J=8.4Hz,2H)IR(KBr)3547,3492,3451,1521,1487,1385,1288,1249,1209,1108,1011,746,702cm-1 |
I-710 | mp178-180℃1H NMR(CDCl3)δ2.43(br s,1H),3.44(s,3H),3.72(s,3H),4.52(m,2H),4.93(s,1H),5.15(s,2H),5.70(s,1H),6.79(dd,J=8.1,2.1Hz,1H),6.84(s,1H),6.92(d,J=8.7Hz,2H),6.93(d,J=2.1Hz,1H),7.00(d,J=8.7Hz,1H),7.38-7.48(m,5H),7.54(d,J=9.0Hz,2H)IR(KBr)3447,3214,1609,1518,1477,1459,1391,1260,1221,1008,984,833,799,751cm-1 |
I-711 | 泡沫1H NMR(CDCl3)δ2.85(s,3H),3.22(s,3H),3.30(s,3H),3.54(s,3H),3.78(s,3H),5.02(s,2H),6.85(s,1H),7.08(d,J=8.4Hz,1H),7.32(d,J=2.1Hz,1H),7.37(dd,J=8.4,2.1Hz,1H),7.39(d.J=8.7Hz,2H),7.67(d,J=8.7Hz,2H)IR(Nujol)3423,3320,3215,1610,1519,1480,1454,1176,1151,1080,969,876,798cm-1 |
I-712 | 泡沫1H NMR(CDCl3)δ2.62(s,3H),3.45(s,3H),3.74(s,3H),5.28(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.95(dd,J=8.4,2.1Hz,1H),7-10(d,J=8.4Hz,1H),7.11(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H),8.50(brs,1H),8.60(brs,1H)IR(Nujol)3207,1611,1589,1523,1489,1460,1227,1116,1072,1014,943,822,759cm-1 |
I-713 | mp231-233℃1H NMR(CDCl3)δ3.30(s,3H),3.64(s,3H),5.28(s,2H),6.39(s,1H),6.67(dd,J=8.4,2.1Hz,1H),6.80(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),7.01(d,J=8.4Hz,1H),7.44(d,J=8.7Hz,2H),8.64(d,J=2.4Hz,1H),8.67(dd,J=2.4,1.2Hz,1H),8.94(d,J=1.2Hz,1H)IR(Nujol)3369,3164,1612,1600,1585,1522,1493,1385,1255,1118,1073,1013,934,824,798,778cm-1 |
I-714 | 泡沫1H NMR(CDCl3)δ2.83(s,3H),3.22(s,3H),3.27(s,3H),3.55(s,3H),3.78(s,3H),5.18(s,2H),6.85(s,1H),7.20(d,J=8.4Hz,1H),7.39(d,J=8.7Hz,2H),7.40(dd,J=8.4,2.1Hz,1H),7.45(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(Nujol)3264,1650,1607,1517,1480,1175,1150,1078,946,876,798cm-1 |
I-715 | 泡沫1H NMR(CDCl3)δ2.76(s,3H),2.77(s,3H),3.21(s,3H),3.24(s,3H),3.55(s,3H),3.78(s,3H),5.35(s,2H),6.84(s,1H),7.25(d,J=8.4Hz,1H),7.38(1,J=8.7Hz,2H),7.38(dd,J=8.4,2.1Hz,1H),7.44(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1607,1578,1519,1465,1176,1151,1079,971,947,876,846,797cm-1 |
I-716 | mp227-229℃1HNMR(DMSO-d6)δ2.87(s,3H),3.39(s,3H),3.45(s,3H),3.52(s,3H),3.79(s,3H),5.23(s,2H),7.08(s,1H),7.33(d,J=2.1Hz,1H),7.35(dd,J=8.4,2.1Hz,1H),7.44(d,J=8.4Hz,1H),7.49(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)3276,1651,1605,1520,1480,1463,1174,1150,1079,947,879,798cm-1 |
I-717 | m.p180-181℃1H NMR(CDCl3)δ3.07(8,3H),3.45(s,3H),3.75(s,3H),5.18(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.99(dd,J=1.8,8.4Hz,1H),7.08(d,J=1.8Hz,1H),7.10(d,J=8.4Hz,1H),7.25(t,J=7.2Hz,1H),7.44(m,2H),7.53(d,J=8.7Hz,2H),7.61(d,J=8.1Hz,1H) |
I-718 | 泡沫1H NMR(CDCl3)δ3.06(s,3H),3.45(s,3H),3.74(s,3H),5.17(s,2H),6.45(s,1H),6.93(d,J=8.7Hz,2H),6.98(dd,J=8.7Hz,1H),7.08(d,J=2.1Hz,1H),7.10(d,J=8.4Hz,1H),7.24(m,1H),7.43(m,2H),7.51(d,J=8.7Hz,2H),7.61(m,1H)IR(KBr)3430,1611,1590,1523,1490,1402,1323,1242,1149,1112,1070,1010,971,826cm-1 |
I-719 | 泡沫1H NMR(CDCl3)δ2.80(s,6H),3.47(s,3H),3.76(s,3H),5.08(s,2H),6.46(s,1H),6.92(d,J=8.7Hz,3H),7.10(d,J=2.1Hz,1H),7.15(d,J=8.7Hz,1H),7.20(d,J=7.2Hz,1H),7.34-7.45(m,3H),7.55(d,J=8.7Hz,2H)IR(Br)3427,1611,1585,1522,1488,1404,1224,1113,1069,1011,940,824,767cm-1 |
I-720 | 泡沫1H NMR(CDCl3)δ1.52(s,9H),2.67(s,3H),3.19(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.17(s,2H),6.54(br.s,1H),7.11(m,1H),7.12(d,J=9.0Hz,1H),7.25(m,1H),7.30(d,J=7.5Hz,1H),7.32(dd,J=1.8,9.0Hz,1H),7.36(d,J=8.7Hz,2H),7.41(d,J=1.8Hz,1H),7.60(s,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1724,1610,1520,1481,1366,1234,1177,1153,1079,969,875,797cm-1 |
I-721 | m.p187-191℃1H NMR(CDCl3)δ2.66(s,3H),3.17(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.11(s,2H),6.65(d,J=8.4Hz,1H),6.81(m,2H),6.84(s,1H),7.12(d,J=8.7Hz,1H),7.17(t,J=8.7Hz,1H),7.32(dd,J=2.1,8.7Hz,1H),7.37(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1624,1606,1519,1481,1361,1176,1148,1081,980,876,780cm-1 |
I-722 | m.p143-146℃1H NMR(CDCl3)δ2.18(s,3H),2.71(s,3H),3.18(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.18(s,2H),6.84(s,1H),7.12(d,J=8.7Hz,1H),7.17(d,J=7.2Hz,1H),7.33(m,2H),7.37(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.45(d,J=7.2Hz,1H),7.67(d,J=8.7Hz,2H),7.67(m,1H)IR(KBr)1693,1609,1519,1481,1364,1364,1173,1149,1079,874,802cm-1 |
I-723 | 泡沫1H NMR(CDCl3)δ2.86(s,3H),3.00(s,3H),3.22(s,3H),3.55(s,3H),3.78(s,3H),5.22(s,2H),6.59(s,1H),6.85(s,1H),7.10(d,J=8.4Hz,1H),7.25(m,3H),7.32(d,J=2.1,8.7Hz,1H),7.37(m,1H),7.38(d,J=2.1Hz,1H),7.38(d,J=8.7Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1610,1519,1480,1364,1176,1150,1079,971,876,797cm-1 |
I-724 | 泡沫1H NMR(CDCl3)δ2.74(s,3H),3.18(s,3H),3.21(s,3H),3.43(s,6H),3.55(s,3H),3.78(s,3H),5.24(s,2H),6.84(s,1H),7.13(d,J=8.4Hz,1H),7.36(dt,J=2.1,8.4Hz,1H),7.37(m,1H),7.39(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.51(m,2H),7.61(s,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1609,1523,1481,1353,1176,1161,1080,890,799cm-1 |
I-725 | m.p147-150℃1H NMR(CDCl3)δ2.79(s,3H),2.83(s,3H),3.20(s,3H),3.21(s,3H),3.35(s,3H),3.55(s,3H),3.78(s,3H),5.22(s,2H),6.85(s,1H),7.11(d,J=8.7Hz,1H),7.32-7.46(m,7H),7.62(s,1H),7.67(d,J=8.4Hz,2H)IR(KBr)1608,1518,1480,1364,1178,1153,1077,968,795cm-1 |
I-726 | m.p224-226℃1H NMR(CDCl3)δ2.85(s,3H),2.91(s,6H),3.36(s,3H),3.45(s,3H),3.51(s,3H),3.78(s,3H),5.19(s,2H),6.69(d,J=8.1Hz,1H),6.76(d,J=8.1Hz,1H),6.89(s,1H),7.07(s,1H),7.20(t,J=8.1Hz,1H),7.30(m,3H),7.48(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(KBr)1608,1519,1480,1360,1178,1146,1081,879,826cm-1 |
I-727 | 泡沫1H NMR(CDCl3)δ2.82(s,3H),3.18(s,6H),3.21(s,3H),3.53(s,3H),3.76(s,3H),5.17(s,2H),6.84(s,1H),7.11(d,J=8.4Hz,1H),7.20(d,J=4.8Hz,1H),7.30-7.47(m,8H),7.76(d,J=8.7Hz,2H)IR(KBr)3430,1677,1609,1519,1481,1364,1202,1177,1150,1079,876,799cm-1 |
I-728 | 泡沫1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.06(s,2H),6.45(s,1H),6.68(d,J=7.5Hz,1H),6.77(s,1H),6.82(d,J=7.5Hz,1H),6.91(d,J=8.7Hz,2H),6.93(dd,J=1.8,8.4Hz,1H),6.99(d,J=8.4Hz,1H),7.07(d,J=1.8Hz,1H),7.19(t,J=7.5Hz,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3413,1611,1522,1488,1461,1405,1251,1119,1076,1007,813,784cm-1 |
I-729 | m.p90-93℃1H NMR(CDCl3)δ3.01(s,3H),3.45(s,3H),3.75(s,3H),5.16(s,2H),6.45(s,1H),6.81(s,1H),6.92(d,J=8.7Hz,2H),6.95(d,J=1.8Hz,1H),6.96(m,2H),7.24(m,2H),7.40(t,J=7.2Hz,1H),7.52(d,J=8.7Hz,2H)IR(KBr)3434,1612,1592,1523,1489,1325,1248,1224,1147,1113,1070,1010,972cm-1 |
I-730 | mp79-81℃1H NMR(CDCl3)δ2.34(s,6H),3.48(s,3H),3.76(s,3H),4.72(brs,1H),5.16(s,2H),5.68(brs,1H),5.93(brs,1H),6.44(s,1H),6.99-7.10(m,3H),7.26-7.49(m,7H)IR(KBr)3467,2933,1613,1701,1517,1482,1454,1424,1389,1321,1196,1148,1113,1073cm-1 |
I-731 | mp189-191℃1H NMR(CDCl3)δ3.20(s,3H),3.81(s,6H),5.14(s,2H),5.65(brs,1H),6.79(s,2H),6.79-7.02(m,5H),7.36-7.46(m,6H),7.66(d,J=8.6Hz,2H)IR(KBr)3439,2937,1594,1567,1523,1487,1351,1240,1202,1146,1126,874cm-1 |
I-732 | mp196-197℃1H NMR(DMSO-d6)δ3.32(s,3H),3.43(s,6H),3.79(s,6H),5.24(s,2H),7.00(s,2H),7.23-7.30(m,3H),7.35-7.55(m,7H),7.88(d,J=8.4Hz,2H)IR(KBr) 3434,1602,1561,1523,1485,1362,1288,1238,1201,1181,1148,1126,1115,966,914,813cm-1 |
I-733 | mp202-203℃1H NMR(DMSO-d6)δ2.40(s,6H),3.31(s,3H),3.34(s,3H),3.51(s,3H),3.58(s,3H),3.77(s,3H),5.27(s,2H),7.03(s,1H),7.32-7.530(m,10H)IR(KBr) 3434,3028,2944,1515,1475,1463,1361,1290,1272,1247,1179,1085,967,815,804cm-1 |
I-734 | mp140-141℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.21(s,3H),3.83(s,6H),4.63(d,J=4.6Hz,2H),5.52-5.53(m,1H),6.79(s,2H),7.05(d,J=8.8Hz,1H),7.29-7.42(m,4H),7.67(d,J=8.6Hz,2H)IR(KBr)3434,2936,1602,1565,1487,1365,1242,1182,1152,1123,1113,974,874,811cm-1 |
I-735 | mp168-169℃1H NMR(CDCl3)δ2.38(s,3H),3.09(s,3H),3.20(s,3H),3.81(s,6H),5.11(s,2H),6.78(s,2H),713-7.42(m,9H),7.66(d,J=8.8Hz,2H)IR(KBr)3433,1601,1566,1486,1367,1246,1182,1153,1114,973,869,824cm-1 |
I-736 | mp192-194℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.47(s,6H),2.72(s,3H),3.24(s,3H),3.36(s,3H),3.57(s,3H),3.79(s,3H),4.64(d,J=6.6Hz,2H),5.47-5.55(m,1H),6.83(s,1H),7.09(d,J=9.0Hz,1H),7.33-7.40(m,4H)IR(KBr)3435,1942,1516,1474,1382,1357,1288,1178,1096,966,862,805cm-1 |
I-737 | mp224-225℃1H NMR(CDCl3)δ2.38(s,3H),2.46(s,6H),2.66(s,3H),3.12(s,3H),3.35(s,3H),3.55(s,3H),3.77(s,3H),5.14(s,2H),6.82(s,1H),712-7.40(m,9H)IR(KBr)3435,2941,1518,1474,1360,1274,1179,1095,1085,967,862,815,805cm-1 |
I-738 | mp203-204℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.46(s,6H),2.45-2.58(m,2H),2.73(s,3H),3.22(s,3H),3.35(s,3H),3.55(s,3H),3.77(s,3H),4.07(d,J=6.6Hz,2H),5.18-5.25(m,1H),6.82(s,1H),7.07(d,J=8.2Hz,1H),7.32-7.39(m,4H)IR(KBr)3434,2941,1519,1473,1359,1276,1178,1114,1085,967,860,811cm-1 |
I-739 | mp158-159℃1H NMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),3.72(s,6H),4.54(d,J=6.0Hz,2H),5.45-5.52(m,1H),6.55-6.59(m,2H),6.84-6.90(m,5H),7.57(d,J=8.2Hz,2H),8.70(brs,1H),9.53(brs,1H)IR(KBr)3465,2932,1610,1523,1487,1460,1283,1281,1123,1010,819cm-1 |
I-740 | mp180-181℃1H NMR(CDCl3)δ2.32(s,3H),3.72(s,6H),5.08(s,2H),6.54-6.58(m,1H),6.68(s,1H),6.85-6.95(m,5H),7.21(d,J=7.6Hz,2H),7.39(d,J=7.8Hz,2H),7.57(d,J=8.4Hz,2H),8.83(brs,1H),9.54(brs,1H)IR(KBr)3519,2937,1607,1562,1523,1461,1400,1246,1176,1125,1003,821cm-1 |
I-741 | mp105-106℃1H NMR(CDCl3)δ2.13(s,6H),3.17(s,3H),5.16(s,2H),5.85(brs,1H),6.61-6.66(m,1H),6.77(s,1H),7.01(d,J=8.2Hz,1H),7.25-7.46(m,9H),7.65(d,J=8.8Hz,2H)IR(KBr)3466,3031,2934,1585,1513,1476,1366,1285,1198,1175,1148,1127,1014,968,868,840cm-1 |
I-742 | mp92-93℃1H NMR(DMSO-d6)δ1.74(s,3H),1.78(s,3H),2.24(s,6H),3.31(s,3H),3.65(s,3H),4.56(d,J=6.8Hz,2H),5.52(t,J=6.0Hz,1H),6.37(s,1H),6.64-6.76(m,2H),6.88-6.93(m,1H),7.16-7.20(m,2H),8.31(brs,1H),8.45(brs,1H),8.73(brs,1H)IR(KBr)3443,2932,1707,1613,1516,1484,1462,1387,1280,1243,1196,1114,1074,979cm-1 |
I-743 | mp180-181℃1H NMR(DMSO-d6)δ2.22(s,6H),2.32(s,3H),3.29(s,3H),3.63(s,3H),5.08(s,2H),6.61-6.65(m,1H),6.75(s,1H),6.93(d,J=8.2Hz,1H),7.13-7.22(m,4H),7.39(d,J=7.4Hz,2H),8.30(brs,1H),8.44(brs,1H),8.84(brs,1H)IR(KBr)3443,2930,1686,1614,1587,1518,14863,1462,1385,1281,1246,1197,1113,1073,1009,806cm-1 |
I-744 | mp123-124℃1H NMR(DMSO-d6)δ1.65(s,3H),1.71(s,3H),2.23(s,6H),2.36-2.51(m,2H),3.31(s,3H),3.64(s,3H),3.91-3.98(m,2H),5.22-5.28(m,1H),6.36(s,1H),6.65-6.88(m,3H),7.16(s,1H),8.30(brs,1H),8.44(brs,1H),8.70(brs,1H)IR(KBr)3444,2930,1686,1613,1518,1483,1390,1283,1248,1198,1113,1074,1013cm-1 |
I-745 | mp174-177℃1H NMR(CDCl3)δ1.77-1.78(d,J=0.9Hz,3H),1.82-1.83(d,J=0.9Hz,3H),2.74(s,3H),3.18(s,3H),3.25(s,3H),3.57(s,3H),3.78(s,2H),4.64-4.67(d,J=6.9Hz,2H),5.51(m,1H),6.86(s,1H),7.09(d,J=8.4Hz,1H),7.35-7.40(m,2H),7.45-7.49(m,2H),7.55-7.60(m,2H)IR(CHCl3)2939,1613,1519,1480,1371,1331,1292,1251,1176,1150,1118,1082,971,871,849cm-1 |
I-746 | mp134-136℃1H NMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.53-2.60(dt,J=6.6,5.7Hz,2H),2.73(s,3H),3.18(s,3H),3.23(s,3H),3.56(s,3H),3.78(s,3H),4.07-4.11(t,J=5.7Hz,2H),5.22(m,1H),6.86(s,1H),7.07(d,J=9.0Hz,1H),7.35-7.40(m,2H),7.45-7.49(m,2H),7.55-7.61(m,2H)IR(CHCl3)2938,1614,1519,1480,1448,1371,1331,1294,1228,1176,1150,1119,1083,1004,970,870,849,819cm-1 |
I-747 | mp182-183℃1H NMR(CDCl3)δ2.26(s,3H),2.28(s,3H),4.74(s,1H),5.16(s,2H),5.69(s,1H),6.81-6.89(m,3H),6.96-6.99(m,2H),7.10-7.12(d,J=4.8Hz,2H),7.23-7.26(m,2H),7.39-7.45(m,5H)IR(CHCl3)3597,3543,2924,2871,1611,1587,1522,1490,1455,1382,1171,1126,1012,836cm-1 |
I-748 | mp158-161℃1H NMR(CDCl3)δ2.38(s,3H),2.74(s,3H),3.12(s,3H),3.18(s,3H),3.57(s,3H),3.78(s,3H),5.15(s,2H),6.86(s,1H),7.16(d,J=8.7Hz,1H),7.21-7.24(d,J=7.8Hz,1H),7.35-7.40(m,5H),7.45-7.49(m,2H),7.52-7.62(m,2H)IR(CHCl3)2939,1732,1614,1519,1480,1331,1294,1253,1176,1150,1119,1082,1003,970,869,816cm-1 |
I-749 | mp174-176℃1H NMR(CDCl3)δ1.75(s,3H),1.79(s,3H),2.58(s,3H),3.52(s,3H),3.53(s,3H),3.78(s,3H),4.62(d,J=6.9Hz,2H),5.48-5.55(m,1H),6.83(s,1H),6.99(d,J=8.7Hz,1H),7.09(dd,J=1.8,8.1Hz,1H),7.11-7.19(m,2H),7.22(d,J=1.8Hz,1H),7.57-7.65(m,2H)IR(KBr)2932,1602,1519,1485,1385,1368,1174,1086,1015,986,848,804,527cm-1 |
I-750 | mp129-131℃1H NMR(CDCl3)δ1.75(s,3H),1.79(s,3H),3.45(s,3H),3.53(s,3H),3.75(s,3H),4.62(d,J=6.6 Hz,2H),5.24(s,2H),5.50-5.58(m,1H),5.90(s,1H),6.44(s,1H),6.99(d,J=8.7Hz,1H),7.08-7.18(m,3H),7.29(d,J=1.8Hz,1H),7.58-7.64(m,2H)IR(KBr)3361,2953,2934,1522,1488,1460,1391,1230,1154,1121,1071,993,912,817,587cm-1 |
I-751 | mp148-150℃1H NMR(CDCl3)δ1.68(s,3H),1.74(s,3H),2.51-2.60(m,5H),3.53(s,6H),3.77(s,3H),4.02(t,J=7.2Hz,2H),5.19-5.25(m,3H),6.83(s,1H),6.98(d,J=8.4Hz,1H),7.08(dd,J=2.1,8.4Hz,1H),7.11-7.18(m,2H),7.21(d,J=2.1Hz,1H),7.57-7.64(m,2H)IR(KBr)2931,1603,1519,1484,1386,1370,1231,1175,1086,1015,983,961,847,728,526cm-1 |
I-752 | mp99-101℃1H NMR(CDCl3)δ1.68(s,3H),1.73(s,3H),2.55(q,J=7.2Hz,2H),3.44(s,3H),3.54(s,3H),3.75(s,3H),4.04(t,J=7.2Hz,2H),5.20-5.25(m,3H),5.89(s,1H),6.44(s,1H),6.98(d,J=8.1Hz,1H),7.09-7.18(m,3H),7.26-7.27(m,1H),7.58-7.63(m,2H)IR(KBr)3349,2930,1609,1523,1489,1231,1152,1121,1072,994,912,813,588cm-1 |
I-753 | mp115-117℃1H NMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.53(q,J=6.9Hz,2H),2.62(s,3H),3.53(s,3H),3.77(s,3H),4.06(t,J=6.9Hz,2H),5.18-5.25(m,1H),5.70(s,1H),6.83(s,1H),6.89-6.95(m,2H),7.02(d,J=1.2Hz,1H),7.10-7.18(m,2H),7.57-7.65(m,2H)IR(KBr)3545,2931,1604,1520,1485,1370,1249,1232,1175,1084,1012,813,526cm-1 |
I-754 | 1H NMR(CDCl3)δ1.14(t,J=6.9Hz,3H),1.29(t,J=6.9Hz,3H),2.50(s,3H),3.19(s,3H),3.71(q,J=6.9Hz,2H),4.00(q,J=6.9Hz,2H),5.18(s,2H),5.68(s,1H),6.83(s,1H),6.91(dd,J=1.8,8.4Hz,1H),7.00(d,J=8.4Hz,1H),7.04(d,J=1.8Hz,1H),7.32-7.48(m,7H),7.66-7.74(m,2H)IR(CHCl3)3532,2976,1586,1516,1468,1369,1282,1174,1148,1068,1016,967,907,871cm-1 |
I-755 | 无定形粉末1H NMR(CDCl3)δ1.15(t,J=6.9Hz,3H),1.28(t,J=6.9Hz,3H),3.59(q,J=6.9Hz,2H),3.97(q,J=6.9Hz,2H),4.89(s,1H),5.15(s,2H),5.64(s,1H),5.98(s,1H),6.45(s,1H),6.86-6.94(m,2H),6.96-7.04(m,2H),7.12(d,J=2.4Hz,1H),7.35-7.56(m,7H),IR(CHCl3)3534,1610,1521,1488,1383,1169,1116,1064,1018,832cm-1 |
I-756 | mp126-129℃1H NMR(CDCl3)δ1.14(t,J=6.9Hz,3H),1.30(t,J=6.9Hz,3H),1.76(s,3H),1.81(s,3H),2.69(s,3H),3.20(s,3H),3.23(s,3H),3.72(q,J=6.9Hz,2H),4.00(q,J=6.9Hz,2H),4.64(d,J=6.6Hz,2H),5.49(m,1H),6.84(s,1H),7.08(d,J=8.7Hz,1H),7.32-7.42(m,4H),7.56-7.72(m,2H)IR(CHCl3)1609,1516,1467,1369,1267,1229,1175,1148,1115,1069,968,907,871cm-1 |
I-757 | mp123-135℃(dec.)1H NMR(CDCl3)δ1.14(t,J=6.9Hz,3H),1.29(t,J=6.9Hz,3H),2.37(s,3H),2.64(s,3H),3.12(s,3H),3.20(s,3H),3.71(q,J=6.9Hz,2H),4.00(q,J=6.9Hz,2H),5.14(s,2H),6.83(s,1H),7.14(d,J=8.7Hz,1H),7.18-7.24(m,2H),7.31-7.40(m,5H),7.41(d,J=2.1Hz,1H),7.65-7.72(m,2H)IR(CHCl3)1607,1517,1467,1369,1330,1268,1175,1148,1116,1069,1026,967,907,871cm-1 |
I-758 | 无定形粉末1H NMR(CDCl3)δ1.15(t,J=6.9Hz,3H),1.28(t,J=6.9Hz,3H),1.76(s,3H),1.82(d,J=0.6Hz,3H),3.59(q,J=6.9Hz,2H),3.97(q,J=6.9Hz,2H),4.61(d,J=6.9Hz,2H),4.87(s,1H),5.53(m,1H),5.66(s,1H),5.97(s,1H),6.45(s,1H),6.86-7.00(m,4H),7.09(d,J=1.8Hz,1H),7.50-7.57(m,2H)IR(CHCl3)3528,2978,1611,1521,1487,1412,1383,1168,1115,1064,905,831cm-1 |
I-759 | 无定形粉末1H NMR(CDCl3)δ1.15(t,J=6.9Hz,3H),1.27(t,J=6.9Hz,3H),2.39(s,3H),3.59(q,J=6.9Hz,2H),3.97(q,J=6.9Hz,2H),4.88(s,1H),5.10(s,2H),5.64(s,1H),5.97(s,1H),6.45(s,1H),6.97-7.01(m,2H),7.11(d,J=1.5Hz,1H),7.20-7.26(m,2H),7.32-7.37(m,2H),7.50-7.56(m,2H)IR(CHCl3)3526,2974,1612,1520,1488,1412,1383,1285,1246,1116,1065,1027,870cm-1 |
I-760 | mp169-171℃1H NMR(CDCl3)δ2.71(s,3H),3.01(s,3H),3.10(s,3H),3.21(s,3H),3.36(s,3H),3.56(s,3H),3.77(s,3H),4.83(s,2H),6.84(s,1H),7.05(d,J=8.4Hz,1H),7.32(dd,J=2.1,8.4Hz,1H),7.36-7.42(m,2H),7.42(d,J=2.1Hz,1H),7.65-7.72(m,2H)IR(CHCl3)1666,1517,1479,1368,1175,1148,1119,1083,1014,968,871cm-1 |
I-761 | mp175-177℃1H NMR(DMSO-d6)δ1.70(s,6H),3.67-3.73(m,2H),3.71(s,3H),3.72(s,3H),4.59(br,1H),5.27-5.31(m,1H),6.50(d,J=8.1Hz,1H),6.77-6.95(m,6H),7.34-7.40(m,2H),9.23(brs,1H),9.42(br s,1H)IR(KBr)3600-2400(br),1609,1522,1492,1463,1384,1263,1208,1174,1129,1055,1033cm-1 |
I-762 | mp151-153℃1H NMR(CDCl3)δ1.78(s,3H),1.85(s,3H),3.78(s,3H),3.80(s,3H),4.72(d,J=6.9Hz,2H),5.39-5.44(m,1H),6.53(d,J=3.0Hz,1H),6.95(s,1H),7.05(s,1H),7.09-7.16(m,3H),7.38(d,J=8.7Hz,1H),7.45(dd,J=1.8,8.7Hz,1H),7.54-7.60(m,2H),7.80(d,J=1.8Hz,1H),IR(KBr)3600-2800(br),1509,1496,1481,1462,1447,1383,1207,1158,1051cm-1 |
I-763 | mp138-139℃1H NMR(CDCl3)δ3.78(s,3H),3.79(s,3H),6.64(dd,J=0.9,2.7Hz,1H),6.80(d,J=7.8Hz,1H),6.94(s,1H),7.04(s,1H),7.09-7.21(m,3H),7.25-7.27(m,1H),7.32(d,J=8.7Hz,1H),7.42(dd,J=1.8,8.4Hz,1H),7.53-7.59(m,3H),8.60-8.63(m,1H)IR(KBr)3600-2800(br),1590,1510,1497,1478,1430,1384,1209,1158,1053,1026cm-1 |
I-764 | mp172-174℃1H NMR(CDCl3)δ2.32(s,3H),3.78(s,3H),3.79(s,3H),5.30(s,2H),6.59(d,J=3.3Hz,1H),6.94(s,1H),7.04(s,1H),7.04-7.15(m,7H),7.34(d,J=8.4Hz,1H),7.41(dd,J=1.8,8.7Hz,1H),7.55-7.59(m,2H),7.82-7.83(m,1H)IR(KBr)3600-2800(br),1516,1497,1482,1466,1382,1306,1219,1209,1159,1051,1026cm-1 |
I-765 | mp134-136℃1H NMR(DMSO-d6)δ1.70(s,3H),1.71(s,3H),3.72-3.74(m,2H),3.73(s,3H),3.74(s,3H),5.25(br s,1H),5.50-5.58(m,1H),6.66-6.72(m,1H),6.78-6.83(m,1H),6.92(s,3H),6.95(s,3H),7.19-7.29(m,2H),7.30-7.39(m,2H),9.45(br s,3H),IR(KBr)3600-2800(br),1624,1610,1526,1494,1461,1382,1255,1208,1175,1120,1054,1031cm-1 |
I-766 | mp166-168℃1H NMR(CDCl3)δ2.40(s,3H),3.77(s,6H),4.82(s,1H),6.71(d,J=2.4Hz,1H),6.86-6.93(m,4H),7.22-7.32(m,4H),7.43-7.48(m,2H),7.58-7.64(m,1H),7.71-7.75(m,2H)IR(KBr)3600-2800(br),1611,1524,1492,1382,1336,1265,1209,1162,1090,1053,1030cm-1 |
I-767 | mp139-140℃1H NMR(CDCl3)δ3.78(8,3H),3.80(s,3H),6.60-6.62(m,1H),6.95(s,1H),7.05(s,1H),m),7.08-7.16(m,2H),7.23-7.26(m,1H),7.45(d,J=1.2Hz,2H),7.54-7.61(m,2H),7.83(d,J=0.6Hz,1H),8.18(br s,1H)IR(KBr)3600-2800(br),1520,1497,1465,1448,1414,1383,1313,1218,1205,1159,1048,1024cm-1 |
I-768 | 1H NMR(CDCl3)δ2.26(s,3H),3.48(s,3H),3.75(s,3H),5.16(s,2H),5.69(s,1H),5.89(s,1H),6.45(s,1H),6.94(d.d,J=8.4&2.1Hz,1H),7.02(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.35-7.50(m,8H),8.36-8.44(m,1H)IR(KBr)3384,1592,1525,1487,1455,1397,1312,1250,1122,1102,1069,1011cm-1 |
I-769 | 1H NMR(CDCl3)δ2.26(s,3H),2.68(s,3H),3.13(s,3H),3.56(s,3H),3.78(s,3H),5.19(s,2H),6.84(s,1H),7.15(d,J=8.4Hz,1H),7.30-7.51(m,10H),8.37-8.47(m,1H)IR(KBr)3384,1704,1590,1524,1481,1389,1357,1272,1240,1174,1114,1082,1017cm-1 |
I-770 | 1H NMR(CDCl3)δ2.67(s,3H),2.84(s,3H),3.28(s,3H),3.56(s,3H),3.78(s,3H),6.26(s,1H),6.85(s,1H),7.17(d,J=9.0Hz,1H),7.24-7.33(m,2H),7.35-7.50(m,3H),8.37-8.50(m,1H)IR(KBr)3383,1674,1595,1526,1482,1363,1177,1078,1012cm-1 |
I-771 | 1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.26(s,3H),2.72(s,3H),3.23(s,3H),3.56(s,3H),3.78(s,3H),4.64(d,J=7.2Hz,2H),5.44-5.53(m,1H),6.84(s,1H),7.09(.d,J=8.4Hz,1H),7.30-7.53(m,5H),8.38-8.47(m,1H)IR(KBr)3376,1697,1594,1524,1481,1365,1270,1239,1177,1112,1079,1013cm-1 |
I-772 | 1H NMR(CDCl3)δ2.26(s,3H),2.38(s,3H),2.68(s,3H),3.12(s,3H),3.56(s,3H),3.78(s,3H),5.14(s,2H),6.84(s,1H),7.12-7.50(m,9H),8.35-8.44(m,1H)IR(KBr)3365,1693,1622,1591,1526,1477,1374,1314,1291,1180,1165,1111,1078cm-1 |
I-773 | 1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.26(s,3H),3.48(s,3H),3.75(s,3H),4.62(d,J=6.9Hz,2H),5.46-5.58(m,1H),5.71(s,1H),5.86(s,1H),6.44(s,1H),6.87-7.00(m,2H),7.05(.d,J=1.8Hz,1H),7.33-7.52(m,3H),8.36-8.47(m,1H)IR(KBr)1737,1604,1519,1482,1392,1366,1267,1173,1131,1084,1062,1009cm-1 |
I-774 | 1H NMR(CDCl3)δ:2.25(s,3H),2.38(s,3H),3.48(s,3H),3.75(s,3H),5.10(s,2H),5.12(brs,1H),5.90(s,1H),6.44(s,1H),6.94(.d.d,J=8.4&1.8Hz,1H),7.02(d,J=8.4Hz,1H),7.06(.d,J=1.8Hz,1H),7.18-7.52(m,6H),8.35-8.44(m,1H)IR(KBr)1686,1590,1524,1488,1398,1314,1257,1102,1068,1008cm-1 |
I-775 | 1H NMR(CDCl3)δ3.47(s,3H),3.76(s,3H),5.16(s,2H),5.71(s,1H),5.82(s,1H),6.45(s,1H),6.97(d.d,J=8.4&2.1Hz,1H),7.04(d,J=8.4Hz,1H),7.07(d,J=2.1Hz,1H),7.22-7.30(m,1H),7.33-7.49(m,5H),7.92-7.98(m,1H),8.09-8.14(m,1H),10.44(s,1H)IR(KBr)3492,3459,1692,1605,1518,1486,1388,1294,1238,1200,1115,1100,1070,1008cm-1 |
I-776 | 1H NMR(CDCl3)δ2.35(d,J=1.8Hz,3H),2.68(s,3H),3.13(s,3H),3.23(s,3H),3.78(s,3H),5.19(s,2H),6.82(s,1H),7.04-7.17(m,2H),7.30-7.49(m,9H)IR(KBr)1606,1518,1478,1364,1295,1271,1240,1182,1118,1087,1077,1017cm-1 |
I-777 | 1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.35(s,3H),2.72(s,3H),3.23(s,3H),3.53(s,3H),3.78(s,3H),4.64(d,J=6.6Hz,2H),5.45-5.53(m,1H),6.82(s,1H),7.03-7.14(m,2H),7.32-7.47(m,4H)IR(KBr)1607,1520,1482,1374,1363,1240,1179,1115,1079cm-1 |
I-778 | 1H NMR(CDCl3)δ2.35(d,J=1.2Hz,3H),3.45(s,3H),3.75(s,3H),5.15(s,2H),5.68(s,1H),5.90(s,1H),6.43(s,1H),6.92-7.12(m,4H),7.31-7.50(m,7H)IR(KBr)3536,3398,1609,1587,1518,1487,1244,1192,1110,1071,1010cm-1 |
I-779 | 1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.35(s,3H),3.45(s,3H),3.74(s,3H),4.61(d,J=6.9Hz,2H),5.43-5.60(m,1H),6.43(s,1H),6.87-7.15(m,4H),7.36-7.51(m,2H)IR(KBr)3512,3444,1611,1585,1518,1488,1462,1447,1416,1305,1288,1243,1207,1112,1103,1070,1012cm-1 |
I-780 | 1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.84(s,2H),5.15(s,2H),5.70(s,1H),5.88(s,1H),6.44(s,1H),6.91-7.20(m,4H),7.32-7.48(m,5H),7.52-7.61(m,1H),7.64-7.74(m,1H)IR(KBr)3523,3428,1610,1587,1516,1482,1463,1400,1321,1285,1238,1187,1106cm-1 |
I-781 | 1H NMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.54(s,3H),3.78(s,3H),5.19(s,2H),5.44(d.d,J=18&0.6Hz,1H),5.90(d.d,J=18&0.9Hz,1H),6.84(s,1H),6.86-6.98(m,1H),7.09-7.18(m,2H),7.31-7.52(m,8H),7.71(d.d,J=7.2&2.4Hz,1H)IR(KBr)1608,1518,1479,1365,1235,1177,1118,1079,1013cm-1 |
I-782 | 1H NMR(CDCl3)δ1.59(d,J=6.3Hz,3H),2.68(s,3H),3.13(s,3H),3.55(s,3H),3.78(s,3H),5.19(s,2H),5.21-5.30(m,1H),6.84(s,1H),7.08-7.17(m,3H),7.32-7.56(m,7H),7.69-7.75(m,1H)IR(KBr)3543,3433,1609,1518,1480,1364,1235,1178,1117,1078,1014cm-1 |
I-783 | 1H NMR(CDCl3)δ1.59(d,J=6.0Hz,3H),2.01(brs,1H),3.47(s,3H),3.76(s,3H),5.16(s,2H),5.15-5.30(m,1H),5.72(s,1H),5.91(s,1H),6.46(s,1H),6.89-7.16(m,4H),7.30-7.60(m,6H),7.68-7.85(m,1H)IR(KBr)3467,1613,1586,1517,1484,1455,1421,1395,1287,1238,1111,1070,1010cm-1 |
I-784 | 1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.23(s,3H),3.81(s,6H),4.64(d,J=6.6Hz,2H),5.47-5.54(m,1H),6.91(s,1H),6.96(s,1H),7.06(.d,J=8.4Hz,1H),7.49(d.d,J=8.4&2.1Hz,1H),7.58(d,J=2.1Hz,1H),7.60-7.74(m,4H)IR(KBr)2228,1610,1490,1348,1295,1266,1209,1174,1112,1056,1038,1000cm-1 |
I-785 | mp169-170℃1H NMR(CDCl3)δ2.07(s,6H),3.20(s,3H),5.16(s,2H),5.71(brs,1H),6.97-7.45(m,14H)IR(KBr)3357,3023,2933,1698,1516,1478,1362,1260,1227,1152,1132,962,869cm-1 |
I-786 | mp169-170℃1H NMR(CDCl3)δ2.13(s,6H),3.11(s,3H),3.18(s,3H),5.18(s,2H),7.09-7.47(m,12H),7.64(d,J=9.0Hz,2H)IR(KBr)3434,3035,2938,1516,1474,1362,1290,1197,1182,1174,1149,1114,973,857,842cm-1 |
I-787 | mp156-157℃1H NMR(CDCl3)δ2.08(s,6H),3.12(s,3H),3.21(s,3H),5.18(s,2H),7.12-7.58(m,14H)IR(KBr)3494,3292,3033,2934,1753,1712,1517,1478,1358,1294,1261,1173,1151,967,870cm-1 |
I-788 | mp105-106℃1H NMR(CDCl3)δ1.75(s,3H),1.85(s,3H),2.12(s,6H),3.18(s,3H),3.22(s,3H),4.64(d,J=7.0Hz,2H),5.52(t,J=6.8Hz,1H),7.08(s,1H),7.16-7.38(m,6H),7.64(d,J=8.8Hz,2H)IR(KBr)3434,2934,1514,1474 1362,1285,1152,1113,971,916,861,845cm-1 |
I-789 | mp148-149℃1H NMR(CDCl3)δ2.12(s,6H),2.39(s,3H),3.10(s,3H),3.18(s,3H),5.13(s,2H),7.10-7.38(m,11H),7.64(d,J=8.6Hz,2H)IR(KBr)3435,3027,2931,1678,1516,1475,1362,1288,1182,1151,1113,969,916,861cm-1 |
I-790 | mp139-140℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.14(s,6H),2.46-2.58(m,2H),3.14(s,3H),3.19(s,3H),4.07(d,J=7.0Hz,2H),5.16-5.23(m,1H),7.05(s,1H),7.14-7.41(m,6H),7.66(d,J=8.4Hz,2H)IR(KBr)3433,2946,1514,1467,1360,1282,1180,1152,1115,868cm-1 |
I-791 | mp123-124℃1H NMR(DMSO-d6)δ1.72(s,3H),1.77(s,3H),2.03(s,6H),4.56(d,J=6.6Hz,2H),5.50(t,J=6.0Hz,1H),6.49(d,J=9.6Hz,1H),6.55(s,1H),6.83(d,J=8.4Hz,2H),6.98(d,J=8.1Hz,1H),7.27(s,2H),7.48(d,J=5.6Hz,2H),8.92(brs,1H),9.48(brs,1H)IR(KBr)3337,2930,1612,1518,1471,1285,1258,1207,1123,999,834cm-1 |
I-792 | mp230-231℃1H NMR(DMSO-d6)δ2.04(s,6H),2.33(s,3H),5.09(s,2H),6.50(d,J=8.4Hz,1H),6.59(s,1H),6.85(d,J=8.1Hz,2H),7.04(d,J=5.4Hz,1H),7.23(d,J=7.5Hz,2H),7.29(s,1H),7.41(d,J=7.8Hz,2H),7.49(d,J=8.7Hz,2H),9.05(brs,1H),9.50(brs,1H)IR(KBr)3287,1609,1519,1475,1298,1245,1126,1006,841cm-1 |
I-793 | mp118-119℃1H NMR(DMSO-d6)δ1.64(s,3H),1.70(s,3H),2.03(s,6H),2.42-2 50(m,2H),3.96(t,J=6.9Hz,2H),5.27(t,J=7.2Hz,2H),6.49(d,J=8.1Hz,1H),6.55(s,1H),6.84(d,J=8.4Hz,2H),6.96(d,J=8.1Hz,1H),7.27(s,2H),7.48(d,J=8.7Hz,2H),8.89(brs,1H),9.48(brs,1H)IR(KBr)3392,2928,1610,1519,1466,1250,1230,1205,1178,1128,1031,834,808cm-1 |
I-794 | mp139-140℃1H NMR(DMSO-d6)δ1.75(s,3H),1.77(s,3H),2.50(s,6H),3.39(s,3H),3.44(s,3H),4.69(d,J=6.2Hz,2H),5.50(t,J=6.6Hz,1H),7.29-7.33(m,3H),7.41-7.47(m,4H),7.59-7.68(m,2H)IR(KBr)3433,2933,1675,1516,1473,1366,1358,1292,1259,1182,1172,1151,969,873cm-1 |
I-795 | mp151-152℃1H NMR(DMSO-d6)δ2.05(s,6H),2.18(s,3H),3.36(s,3h),3.44(s,3H),5.22(s,2H),7.08-7.63(m,13H)IR(KBr)3434,3023,2928,1517,1477,1368,1293,1261,1183,1152,966,870cm-1 |
I-796 | mp159-160℃1H NMR(DMSO-d6)δ1.65(s,3H),1.70(s,3H),2.05(s,6H),2.48-2.53(m,2H),3.38(s,3H),3.44(s,3H),4.10(t,J=7.4Hz,2H),5.21-5.27(m,1H),7.28-7.34(m,3H),7.41-7.47(m,4H),7.59-7.64(m,2H)IR(KBr)3434,2938,1519,1478,1439,1362,1295,1269,1173,1152,1125,960,870,839cm-1 |
I-797 | mp130-131℃1H NMR(DMSO-d6)δ1.72(s,3H),1.75(s,3H),2.02(s,6H),4.59(d,J=6.4Hz,2H),5.48(t,J=7.2Hz,1H),6.81-7.07(m,7H),7.25(s,2H),8.96(brs,1H),9.41(brs,1H)IR(KBr)3392,1608,1589,1518,1475,1322,1258,1170,1127,974,836,808cm-1 |
I-798 | mp143-144℃1H NMR(DMSO-d6)δ2.03(s,6H),2.32(s,3H),5.12(s,2H),6.82-7.41(m,13H),9.10(brs,1H),9.41(brs,1H)IR(KBr)3344,1609,1521,1427,1255,1236,1205,1129,998,832,806,792cm-1 |
I-799 | mp163-164℃1H NMR(DMSO-d6)δ1.87(s,3H),1.90(s,3H),3.42(s,3H),5.15(s,2H),6.88-7.03(m,4H),7.24-7.58(m,9H),7.97(brs,1H),9.02(brs,1H)IR(KBr) 3563,3476,3001,2922,1698,1527,1512,1476,1359,1303,1261,1237,1210,1195,1167,1146,871cm-1 |
I-800 | 1H NMR(CDCl3)δ1.30(d,J=6.6Hz,6H),2.58(s,3H),2.97(quintet,J=6.6Hz,1H),3.54(s,3H),3.77(s,3H),5.17(s,2H),6.87(s,1H),7.11(d,J=9.0Hz,1H),7.22-7.35(m,8H),7.47-7.68(m,6H),8.19-8.25(m,2H)IR(KBr)1737,1604,1519,1482,1392,1366,1267,1173,1131,1084,1062,1009cm-1 |
I-801 | 1H NMR(CDCl3)δ2.56(s,3H),3.55(s,3H),3.78(s,3H),5.17(s,2H),5.69(s,1H),6.84(s,1H),6.91(d.d,J=8.4&1.8Hz,1H),7.02(d,J=8.4Hz,1H),7.04(d,J=1.8Hz,1H),7.04-7.14(m,1H),7.33-7.47(m,8H)IR(KBr)3446,1613,1585,1522,1477,1396,1357,1291,1243,1204,1174,1076,1017,1006cm-1 |
1-802 | 泡沫1H NMR(CDCl3)δ2.82(s,3H),3.22(s,3H),3.25(s,3H),3.26(s,3H),3.55(s,3H),3.78(s,3H),5.48(s,2H),6.85(s,1H),7.27(d,J=8.4Hz,1H),7.39(d,J=8.7Hz,2H),7.40(dd,J=8.4,2.1Hz,1H),7.43(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(Nujol)1608,1519,1480,1462,1365,1176,1151,1079,970,876,798cm-1 |
I-803 | 泡沫1H NMR(CD3OD)δ3.28(s,3H),3.68(s,3H),5.17(s,2H),6.43(s,1H),6.81(dd,J=8.4,2.1Hz,1H),6.85(d,J=8.7Hz,2H),6.89(d,J=2.1Hz,1H),7.03(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3342,1611,1592,1523,1488,1460,1251,1225,1114,1072,1012,941,826,756cm-1 |
I-804 | mp150-152℃1H NMR(DMSO-d6)δ3.31(s,3H),3.64(s,3H),5.00(s,2H),6.39(s,1H),6.66(dd,J=8.4,2.1Hz,1H),6.79(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),6.98(d,J=8.4Hz,1H),7.44(d,J=8.7Hz,2H)IR(Nujol)3459,3291,1612,1594,1522,1489,1458,1257,1226,1101,1073,1011,960,823cm-1 |
I-805 | mp190-192℃1H NMR(DMSO-d6)δ2.88(s,3H),3.41(s,3H),3.45(s,3H),3.52(s,3H),3.79(s,3H),5.43(s,2H),7.08(s,1H),7.16(s,1H),7.32~7.36(m,2H),7.46(d,J=8.4Hz,1H),7.49(d,J=8.7Hz,2H),7.53~7.64(m,3H),7.74(d,J=8.7Hz,2H),7.88~7.91(m,2H)IR(Nujol)1604,1519,1481,1462,1367,1175,1081,1009,878,841,816,801cm-1 |
I-806 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.74(s,3H),5.31(s,2H),6.94(s,1H),6.45(s,1H),6.64(s,1H),6.93(d,J=8.7Hz,2H),6.98(dd,J=8.4,2.1Hz,1H),7.09(d,J=8.4Hz,1H),7.11(d,J=2.1Hz,1H),7.46~7.50(m,3H),7.53(d,J=8.7Hz,2H),7.78~7.82(m,2H)IR(Nujol)3367,1612,1592,1523,1489,1455,1253,1226,1115,1073,1013,942,816,767cm-1 |
I-807 | 泡沫1H NMR(CDCl3)δ2.76(s,3H),3.21(s,3H),3.30(s,3H),3.56(s,3H),3.78(s,3H),5.38(s,2H),6.84(s,1H),7.21(d,J=8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.38(dd,J=8.4,2.1Hz,1H),7.45(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H),8.80(s,1H)IR(Nujol)1608,1519,1480,1463,1365,1177,1151,1079,971,876,798cm-1 |
I-808 | mp193-195℃1H NMR(CDCl3)δ2.64(s,3H),2.74(s,3H),3.21(s,3H),3.30(s,3H),3.56(s,3H),3.78(s,3H),5.28(s,2H),6.84(s,1H),7.21(d,J=8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.38(dd,J=8.4,2.1Hz,1H),7.44(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1606,1591,1522,1480,1463,1359,1174,1152,1079,1012,946,877,834,796cm-1 |
I-809 | 泡沫1H NMR(CDCl3)δ1.42(t,J=7.5Hz,3H),2.73(s,3H),2.96(q,J=7.5Hz,2H),3.21(s,3H),3.31(s,3H),3.56(s,3H),3.78(s,3H),5.28(s,2H),6.84(s,1H),7.21(d,J=8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.38(dd,J=8.4,2.1Hz,1H),7.44(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)3434,1609,1579,1519,1481,1365,1177,1151,1080,970,876,797cm-1 |
I-810 | 泡沫1H NMR(CDCl3)δ2.71(s,3H),3.21(s,3H),3.35(s,3H),3.56(s,3H),3.78(s,3H),5.38(s,2H),6.84(s,1H),7.25(d,J=8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.40(dd,J=8.4,2.1Hz,1H),7.46(d,J=2.1Hz,1H),7.54~7.64(m,3H),7.68(d,J=8.7Hz,2H),8.12~8.16(m,2H)IR(KBr)3433,1609,1561,1519,1480,1365,1177,1151,1081,971,876,798cm-1 |
I-811 | 泡沫1H NMR(CDCl3)δ2.51(s,3H),2.54(s,3H),2.63(s,3H),2.72(s,3H),3.16(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),5.27(s,2H),6.84(s,1H),7.27(d,J=8.4Hz,1H),7.36(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)3435,1614,1519,1480,1364,1177,1151,1080,972,876,798cm-1 |
I-812 | 泡沫1H NMR(CDCl3)δ2.74(s,6H),3.17(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),5.35(s,2H),6.84(s,1H),7.28(d,J=8.4Hz,1H),7.36(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H),8.41(d,J=2.4Hz,1H),8.50(d,J=2.4Hz,1H)IR(KBr)3433,1609,1519,1481,1364,1177,1151,1080,971,876,798cm-1 |
I-813 | 泡沫1H NMR(DMSO-d6)δ2.47(s,6H),2.55(s,3H),3.30(s,3H),3.64(s,3H),5.16(s,2H),6.39(s,1H),6.66(dd,J=8.4,2.1Hz,1H),6.76(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),7.03(d,J=8.4Hz,1H),7.44(d,J=8.7Hz,2H),IR(KBr)3399,3165,1611,1521,1488,1406,1362,1213,1114,1069,1014,818,759cm-1 |
I-814 | mp240-241℃1H NMR(DMSO-d6)δ2.66(s,3H),3.30(s,3H),3.64(s,3H),5.26(s,2H),6.39(s,1H),6.66(dd,J=8.4,2.1Hz,1H),6.77(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),7.02(d,J=8.4Hz,1H),7.44(d,J=8.7Hz,2H),8.48(d,J=2.7Hz,1H),8.53(d,J=2.7Hz,1H)IR(Nujol)3513,3491,3070,1610,1581,1523,1488,1459,1408,1275,1236,1216,1111,1065,1040,821,785cm-1 |
I-815 | mp288-290℃(decomp.)1H NMR(DMSO-d6)δ2.89(s,3H),3.41(s,3H),3.45(s,3H),3.52(s,3H),3.79(s,3H),4.95(s,2H),5.65(s,1H),7.08(s,1H),7.26(d,J=8.4Hz,1H),7.33(dd,J=8.4.2.1Hz,1H),7.38(d,J=2.1Hz,1H),7.49(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H),IR(Nujol)3120,1712,1671,1604,1516,1480,1462,1364,1172,1078,1015,970,874,841,796cm-1 |
I-816 | mp204-206℃1H NMR(DMSO-d6)δ2.87(s,3H),3.45(s,3H),3.46(s,3H),3.52(s,3H),3.78(s,3H),5.40(s,2H),7.08(s,1H),7.32(dd,J=8.4,2.1Hz,1H),7.33(d,J=8.4Hz,1H),7.39(d,J=2.1Hz,1H),7.48(d,J=8.7Hz,2H),7.71(dd,J=5.1,1.2Hz,1H),7.74(d,J=8.7Hz,2H),8.88(d,J=5.1Hz,1H),9.21(d,J=1.2Hz,1H)IR(Nujol)1608,1586,1557,1521,1480,1464,1360,1352,1176,1156,1078,884,835,818,799cm-1 |
I-817 | 泡沫1H NMR(CDCl3)δ2.20(s,3H),3.45(s,3H),3 75(s,3H),5.15(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.94(dd,J=1.8,8.4Hz,1H),6.98(d,J=8.4Hz,1H),7.09(d,J=1.8Hz,1H),7.18(m,1H),7.37(t,J=7.2Hz,1H),7.53(d,J=8.7Hz,2H),7.55(m,2H) |
I-818 | m.p163-166℃1H NMR(CDCl3)δ1.53(s,9H),2.67(s,3H),3.11(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),5.12(s,2H),6.52(s,1H),6.84(s,1H),7.13(d,J=8.4Hz,1H),7.33(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.39(m,5H),7.74(d,J=8.7Hz,2H)IR(KBr)1692,1614,1520,1480,1390,1367,1231,1175,1152,1078,876,799cm-1 |
I-819 | m.p172℃1H NMR(CDCl3)δ2.77(s,3H),3.05(s,3H),3.16(s,3H),3.22(s,3H),3.36(s,3H),3.78(s,3H),5.16(s,2H),6.46(s,1H),6.85(s,1H),7.14(d,J=8.4Hz,1H),7.25(d,J=8.7Hz,2H),7.35(dd,J=2.1,8.4Hz,1H),7.39(d,J=8.7Hz,2H),7.40(d,J=2.1,1H),7.47(d,J=8.4Hz,2H),7.67(d,J=8.7Hz,2H)IR(KBr)1608,1519,1480,1361,1175,1154,1079,972,876,801cm-1 |
I-820 | mp180-182℃1H NMR(CDCl3)δ2.69(s,3H),3.14(s,3H),3.21(s,3H),3.53(s,3H),3.71(d,J=0.9Hz,3H),5.20(s,2H),6.93(d,J=8.4Hz,1H),7.34-7.49(m,9H),7.59(dd,J=9.0,1.2Hz,2H)IR(KBr)1518,1469,1357,1179,1151,1038,871,821cm-1 |
I-821 | mp183-185℃1H NMR(CDCl3)δ3.41(s,3H),3.66(d,J=0.9Hz,3H),4.91(s,1H),5.17(s,2H),5.62(s,1H),5.70(s,1H),6.92-6.96(m,2H),6.97(dd,J=8.4,2.0Hz,1H),7.04(d,J=8.4Hz,1H),7.10(d,J=2.0Hz,1H),7.36-7.48(m,7H)IR(KBr)3541,3398,1588,1523,1461,1410,1320,1261,1217,1037,836,747cm-1 |
I-822 | mp108-110℃1H NMR(CDCl3)δ2.69(s,3H),3.13(s,3H),3.45(s,3H),3.53(s,3H),3.77(s,3H),4.66(s,2H),4.76(s,2H),5.19(s,2H),6.86(s,1H),7.71(d,J=8.4Hz,1H),7.33-7.48(m,9H),7.62(d,J=8.4Hz,2H)IR(KBr)1482,1390,1307,1276,1177,1083,1053,1013,807cm-1 |
I-823 | mp192-194℃1H NMR(CDCl3)δ1.70(brs,1H),2.69(s,3H),3.13(s,3H),3.53(s,3H),3.77(s,3H),4.78(s,2H),5.19(s,2H),6.87(s,1H),7.15(d,J=8.4Hz,1H),7.35(dd,J=8.4,2.3Hz,1H),7.37-7.49(m,8H),7.63(d,J=7.8Hz,2H)IR(KBr)3554,3434,1522,1481,1389,1364,1277,1234,1174,1085,1012,807cm-1 |
I-824 | mp135-137℃1H NMR(CDCl3)δ3.19(s,3H),3.60(s,3H),3.71(s,3H),4.96(s,1H),5.18(s,2H),5.78(s,1H),6.73(s,1H),6.88(dd,J=8.3,2.1Hz,1H),7.02(d,J=2.1Hz,1H),7.08(d,J=8.3Hz,1H),7.34(d,J=8.6Hz,2H),7.41-7.47(m,5H),7.63(d,J=8.6Hz,2H)IR(KBr)3479,1473,1347,1149,1010,869,803,784,747cm-1 |
I-825 | mp149-151℃1H NMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.20(s,3H),3.69(s,3H),3.71(s,3H),5.20(s,2H),7.18(d,J=8.7Hz,1H),7.21(s,1H),7.35-7.50(m,9H),7.63(d,J=8.1Hz,2H)IR(KBr)1519,1469,1353,1173,1149,1050,966,873,849,810cm-1 |
I-826 | mp82-85℃1H NMR(CDCl3)δ1.78(s,3H),1.82(s,3H),2.70(s,3H),3.20(s,3H),3.25(s,3H),3.69(s,3H),3.70(s,3H),4.65(d,J=6.9Hz,2H),5.51(t,J=6.9Hz,1H),7.11(d,J=8.8Hz,1H),7.21(s,1H),7.37(d,J=8.9Hz,2H),7.38(dd,J=8.8,2.2Hz,1H),7.42(d,J=2.2Hz,1H),7.63(d,J=8.9Hz,2H)IR(KBr)1516,1468,1363,1180,1151,1045,967,846,788cm-1 |
I-827 | 无定形1H NMR(CDCl3)δ1.77(s,3H),1.83(s,3H),3.58(s,3H),3.70(s,3H),4.64(d,J=6.7Hz,2H),4.97(s,1H),5.04(s,1H),5.53(t,J=6.7Hz,1H),5.81(s,1H),6.73(s,1H),6.87(dd,J=8.1,2.0Hz,1H),6.88(d,J=8.7Hz,2H),6.99(d,J=2.0Hz,1H),7.00(d,J=8.1Hz,1H),7.47(d,J=8.7Hz,2H)IR(CHCl3)3595,3536,1613,1584,1521,1474,1406,1356,1266,1094,1062,1014,973,835cm-1 |
I-828 | mp161-162℃1H NMR(CDCl3)δ3.58(s,3H),3.71(s,3H),4.85(s,1H),4.93(s,1H),5.18(s,2H),5.78(s,1H),6.73(s,1H),6.87-6.92(m,3H),7.02(d,J=1.8Hz,1H),7.07(d,J=8.1Hz,1H),7.37-7.51(m,7H)IR(KBr)3510,3442,3326,1523,1485,1453,1395,1239,1061,1003,972,836,753cm-1 |
I-829 | mp85-87℃1H NMR(CDCl3)δ1.69(s,3H),1.75(s,3H),2.57(q,J=6.9Hz,2H),2.70(s,3H),3.20(s,3H),3.24(s,3H),3.69(s,3H),3.69(s,3H),4.09(t,J=6.9Hz,2H),5.22(t,J=6.9Hz,1H),7.10(d,J=8.4Hz,1H),7.21(s,1H),7.37-7.44(m,9H),7.63(d,J=8.4Hz,2H)IR(KBr)1519,1468,1362,1179,1150,1046,967,865,847cm-1 |
I-830 | mp160-162℃1H NMR(CDCl3)δ2.38(s,3H),2.68(s,3H),3.12(s,3H),3.20(s,3H),3.69(s,3H),3.70(s,3H),5.15(s,2H),7.16-7.25(m,4H),7.34-7.44(m,6H),7.63(d,J=8.1Hz,2H)IR(KBr)1519,1469,1365,1173,1149,1049,965,873,849,808cm-1 |
I-831 | 无定形1H NMR(CDCl3)δ1.69(s,3H),1.76(s,3H),2.55(q,J=6.9Hz,1H),3.58(s,3H),3.69(s,3H),4.08(t,J=6.9Hz,2H),4.98(s,1H),5.18(s,1H),5.23(t,J=6.9Hz,1H),5.80(s,1H),6.72(s,1H),6.86-6.89(m,3H),6.97-7.00(m,3H),7.47(d,J=8.4Hz,2H)IR(KBr)3595,3538,1521,1471,1265,1173,1095,1063,1015,835cm-1 |
I-832 | mp200-201℃1H NMR(CDCl3)δ2.40(s,3H),3.58(s,3H),3.70(s,3H),4.80(s,1H),4.92(s,1H),5.13(s,2H),5.77(s,1H),6.73(s,1H),6.88(dd,J=8.1,2.0Hz,1H),6.89(d,J=8.4Hz,2H),7.01(d,J=1.8Hz,1H),7.07(d,J=8.4Hz,1H),7.24(d,J=7.8Hz,2H),7.35(d,J=7.8Hz,2H),7.48(d,J=8.4Hz,2H),IR(KBr)3419,1610,1523,1485,1393,1243,1065,1004,972,833,795cm-1 |
I-833 | mp141-142℃1H NMR(CDCl3)δ2.03(s,3H),2.11(s,3H),2.54(s,3H),3.15(s,3H),3.21(s,3H),5.20(s,2H),7.12-7.26(m,5H),7.38-7.50(m,8H)IR(KBr)3435,3033,2938,1518,1470,1364,1178,1149,1109,970,871,839cm-1 |
I-834 | mp188-189℃1H NMR(CDCl3)δ3.49(s,3H),3.72(s,3H),5.15(s,2H),5.68(brs,1H),5.84(brs,1H),6.42-6.56(m,3H),6.98-7.08(m,3H),7.23-7.31(m,3H),7.23-7.31(m,2H),7.38-7.45(m,4H)IR(KBr)3420,3328,1627,1584,1523,1489,1460,1412,1316,1288,1249,1172,1128,1115,1068,1000,849,812,746cm-1 |
I-835 | mp180-181℃1H NMR(CDCl3)δ3.51(s,3H),3.75(s,3H),6.17(s,2H),5.70(brs,1H),5.77(brs,1H),6.45(s,1H),6.95-7.10(m,4H),7.27-7.46(m,8H),7.96(brs,1H))IR(KBr)3422,3358,1706,1602,1489,1454,1410,1289,1253,1203,1180,1125,1101,1071,1015cm-1 |
I-836 | mp148-149℃1H NMR(DMSO-d6)δ1.77(s,3H),1.80(s,3H),2.64(s,6H),3.35(s,3H),3.42(s,3H),3.48(s,3H),4.73(d,J=4.5Hz,2H),5.50-5.53(m,1H),7.30-7.54(m,8H)IR(KBr)3495,3293,1754,1712,1516,1359,1359,1243,1175,1147,971,866,845cm-1 |
I-837 | mp136-138℃1H NMR(DMSO-d6)δ2.32(s,3H),2.50(s,6H),3.31(s,3H),3.35(s,3H),3.44(s,3H),5.23(s,2H),7.21-7.47(m,12H)IR(KBr)3495,3292,3028,2934,1754,1710,1516,1357,1176,1147,972,868,842cm-1 |
I-838 | mp195-196℃1H NMR(CDCl3)δ1.44(t,J=7.2Hz,3H),3.46(s,3H),3.69(s,3H),3.86(s,6H),4.44(q,J=7.0Hz,2H),5.15(s,2H),5.66(brs,1H),5.72(brs,1H),6.27(s,1H),7.01(s,2H),7.13(s,1H),7.38-7.46(m,7H)IR(KBr)3485,2937,1713,1580,1464,1455,1407,1324,1243,1123,11102,1069,1014,763cm-1 |
I-839 | mp150-151℃1H NMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),1.88(s,3H),1.90(s,3H),4.55(d,J=5.8Hz,2H),5.44-5.50(m,1H),6.80-6.97(m,8H),7.81(brs,1H),8.85(brs,1H),9.38(brs,1H)IR(KBr)3495,3293,1753,1711,1429,1390,1360,1242,1217,1178,143,781cm-1 |
I-840 | mp149-150℃1H NMR(DMSO-d6)δ1.71(s,3H),1.75(s,3H),2.00(s,6H),2.59(s,3H),4.57(d,J=6.4Hz,2H),5.42-5.47(m,1H),6.84-7.13(m,8H),9.13(brs,1H),9.50(brs,1H)IR(KBr)3451,2933,1612,1587,1518,1472,1348,1259,1211,1171,1121,1087,969,872,835,813cm-1 |
I-841 | mp203-204℃1H NMR(DMSO-d6)δ1.87(s,3H),1.89(s,3H),2.31(s,3H),5.09(s,2H),6.80-7.00(m,8H),7.20(d,J=7.8Hz,2H),7.39(d,J=7.8Hz,2H),7.81(brs,1H),8.97(brs,1H),9.38(brs,1H)IR(KBr)3491,3398,2921,1611,1516,1476,1259,1183,1155,996,794cm-1 |
I-842 | mp128-129℃1H NMR(DMSO-d6)δ2.01(s,6H),2.34(s,3H),2.63(s,3H),5.12(s,2H),6.85-7.13(m,8H),7.18(d,J=7.6Hz,2H),7.36(d,J=7.6Hz,2H),9.15(brs,1H),9.55(brs,1H)IR(KBr)3432,3305,1735,1607,1523,1482,1398,1360,1294,1284,1179,1080,816cm-1 |
I-843 | mp203-204℃1H NMR(CDCl3)δ2.66(s,3H),3.13(s,3H),3.59(s,3H),3.76(s,3H),5.19(s,2H),6.85(s,1H),7.13-7.69(m,11H),8.07(brs,1H)IR(KBr)3432,3305,1735,1607,1523,1482,1398,1360,1294,1284,1179,1080,816cm-1 |
I-844 | mp109-110℃1H NMR(DMSO-d6)δ1.36(t,J=7.2Hz,3H),2.82(s,3H),3.24(s,3H),3.47(s,3H),3.66(s,3H),3.79(s,6H),4.38(q,J=7.0Hz,2H),5.26(s,2H),6.78(s,1H),7.32-7.52(m,10H)IR(KBr)3432,2940,1716,1579,1465,1407,1366,1322,1240,1179,1123,1078,815,796cm-1 |
I-845 | mp113-115℃1H NMR(CDCl3)δ2.25(s,3H),2.27(s,3H),3.20(s,3H),5.20(s,2H),7.03-7.15(m,5H),7.33-7.51(m,9H))IR(CHCl3)2925,1618,1580,1521,1455,1373,1314,1299,1268,1174,1149,1126,1018,970,874cm-1 |
I-846 | mp155-157℃1H NMR(CDCl3)δ2.26(s,6H),4.69(s,1H),5.19(s,2H),6.87-6.90(m,2H),7.03-7.15(m,5H),7.22-7.50(m,7H)IR(CHCl3)3596,2952,2924,1612,1582,1523,1490,1455,1425,1383,1259,1171,1125,1012,956,877cm-1 |
I-847 | mp81-84℃1H NMR(CDCl3)δ1-07-1.14(m,6H),2.55-2.66(m,4H),4.73(s,1H),5.16(s,2H),5.70(s,1H),6.82-6.91(m,3H),6.92-6.99(m,2H),7.10-7.12(d,J=4.2Hz,2H),7.22-7.25(m,2H),7.38-7.49(m,5H)IR(CHCl3)3596,3542,2968,2932,2872,1731,1611,1588,1520,1489,1455,1380,1327,1289,1256,1171,1126,1011,903,878,836cm-1 |
I-848 | mp125-127℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.26(s,3H),2.28(s,3H),3.20(s,3H),4.63-4.65(d,J=6.9Hz,2H),5.56(m,1H),7.02-7.13(m,5H),7.31-7.43(m,4H)IR(CHCl3)2924,1619,1578,1488,1373,1298,1266,1174,1149,1125,970,874cm-1 |
I-849 | mp141-143℃1H NMR(CDCl3)δ1.07-1.14(m,6H),2.53 2.65(m,4H),3.12(s,3H),3.20(s,3H),5.18(s,2H),7.10-7.14(m,3H),7.24-7.27(m,2H),7.33-7.50(m,9H)IR(CHCl3)2969,2934,1614,1517,1487,1371,1331,1289,1263,1173,1149,1111,970,938,872cm-1 |
I-850 | mp90-91℃1H NMR(CDCl3)δ2.13(s,3H),2.29(s,3H),2.35(s,3H),3.16(s,3H),5.21(s,2H),6.87-6.90(m,2H),7.09-7.49(m,11H)IR(CHCl3)3596,1731,1613,1520,1478,1362,1261,1173,1119,1086,1025,972,953,874cm-1 |
I-851 | mp94-96℃1H NMR(CDCl3)δ1.76-1.77(d,J=0.3Hz,3H),1.81-1.82(d,J=0.9Hz,3H),2.26(s,3H),2.27(s,3H),4.62-4.64(d,J=6.9Hz,2H),4.71(s,1H),5.56(m,1H),6.87-6.91(m,2H),7.00-7.13(m,5H),7.23-7.27(m,2H)IR(CHCl3)3596,2923,1675,1613,1579,1523,1490,1386,1297,1171,1124,990,956,877,836cm-1 |
I-852 | mp106-108℃1H NMR(CDCl3)δ2.63(s,3H),3.52(s,3H),3.77(s,3H),5.24(s,2H),6.84(s,1H),6.84(s,1H),7.12-7.20(m,3H),7.35-7.50(m,7H),7.56-7.64(m,2H)IR(KBr)2935,1604,1523,1483,1373,1232,1086,1011,945,847,728,605,523,506cm-1 |
I-853 | mp136-138℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.67(s,3H),3.53(s,3H),3.78(s,3H),4.67(d,J=6.9Hz,2H),5.47-5.53(m,1H),6.84(s,1H),7.10-7.19(m,3H),7.31(d,J=2.1Hz,1H),7.38(dd,J=2.1,8.1Hz,1H),7.57-7.34(m,2H)IR(KBr)2936,1604,1523,1484,1435,1373,1225,1086,1011,943,848,783,606,508cm-1 |
I-854 | mp128-130℃1H NMR(CDCl3)δ1.74(s,3H),1.81(s,3H),2.62(s,3H),3.52(s,3H),3.79(s,3H),4.63-4.67(m,2H),5.45-5.53(m,1H),6.86(s,1H),7.01(dd,J=2.1Hz,8.4Hz,1H),7.10(d,J=1.8Hz,1H),7.13-7.20(m,2H),7.29(d,J=8.4Hz,1H),7.59-7.64(m,2H)IR(KBr)2940,1600,1518,1484,1418,1366,1232,1080,984,893,838,812,621,524cm-1 |
I-855 | mp141-143℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.61(s,3H),3.53(s,3H),3.77(s,3H),4.62(d,J=6.9Hz,2H),5.47-5.53(m,1H),5.70(s,1H),6.83(s,1H),6.91(dd,J=2.1,8.1Hz,1H),6.96(d,J=8.1Hz,1H),7.02(d,J=2.1Hz,1H),7.10-7.19(m,2H),7.59-7.64(m,2H)IR(KBr)3531,2931,1604,1520,1484,1372,1233,1175,1083,1011,814,800,781,727,526cm-1 |
I-856 | mp217-220℃1H NMR(CDCl3)δ2.75(s,3H),3.51(s,3H),3.78(s,3H),5.78(s,1H),6.85(s,1H),7.03(dd,J=1.8,8.4Hz,1H),7.11-7.20(m,3H),7.32(d,J=8.4Hz,1H),7.58-7.63(m,2H)IR(KBr)3434,2941,1611,1487,1423,1363,1209,1076,891,818,621,573,513cm-1 |
I-857 | mp183-185℃1H NMR(CDCl3)δ1.92(s,3H),3.20(s,3H),3.53(s,3H),3.78(s,3H),3.93(s,3H),4.31(s,4H),6.79-6.83(m,2H),6.90-6.94(m,2H),7.16-7.41(m,12H),7.66-7.71(m,2H),IR(KBr) 3030,2936,1604,1517,1482,1362,1232,1232,1180,1120,1082,877,799,701,526cm-1 |
I-858 | mp192-194℃1H NMR(CDCl3)δ2.57(s,3H),3.21(s,3H),3.56(s,3H),3.77(s,3H),3.87(s,3H),6.77-6.89(m,4H),7.34-7.40(m,2H),7.67-7.72(m,2H)IR(KHr)3451,3368,2937,1622,1524,1481,1359,1174,1149,1086,962,869,802,525cm-1 |
I-859 | mp210-212℃1H NMR(CDCl3)δ1.92(s,3H),2.23(s,3H),3.46(s,3H),3.74(s,3H),3.89(s,3H),5.24(s,1H),5.80(s,1H),5.94(s,1H),6.46(s,1H),6.90-6.96(m,1H),7.01(d,J=1.8Hz,1H),7.08(dd,J=1.8,8.1Hz,1H),7.50-7.55(m,2H),7.76(s,1H),8.52(d,J=8.1Hz,1H),IR(KBr)3420,2938,1636,1610,1526,1496,1398,1225,1164,1073,1026,831cm-1 |
I-860 | mp183-185℃1H NMR(DMSO-d6)δ2.43(s,6H),2.45(s,6H),5.13(s,2H),6.76-6.82(m,4H),6.91(dd,J=2.1,8.4Hz,1H),7.01(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.31-7.43(m,5H),7.48-7.53(m,2H),9.02(brs,1H),9.32(brs,1H)IR(KBr)3600-2800(br),1609,1581,1521,1493,1455,1437,1384,1321,1275,1215,1193,1142,1007cm-1 |
I-861 | mp172-174℃1H NMR(CDCl3)δ2.50(s,6H),2.53(s,6H),3.11(s,3H),3.19(s,3H),5.18(s,2H),6.89(s,1H),6.93(s,1H),7.12(d,J=8.4Hz,1H),7.30-7.54(m,8H),7.66-7.71(m,2H),7.73(d,J=2.1Hz,1H)IR(KBr)3600-2800(br),1613,1518,1491,1455,1361,1348,1276,1178,1159,1109,970cm-1 |
I-862 | mp173-175℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.51(s,6H),2.53(s,6H),3.19(s,3H),3.22(s,3H),4.63(d,J=7.2Hz,2H),5.49-5.53(m,1H),6.89(s,1H),6.93(s,1H),7.05(d,J=9.0Hz,1H),7.26-7.35(m,2H),7.51(dd,J=1.8,8.1Hz,1H),7.67-7.70(m,3H)IR(KBr)3600-2800(br),1519,1491,1363,1331,1291,1257,1175,1147,1105,1013,980,966cm-1 |
I-863 | mp150-152℃1H NMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),2.43(s,6H),2.45(s,6H),4.55(d,J=6.6Hz,2H),5.47-5.51(m,1H),6.78-6.83(m,4H),6.90-7.06(m,3H),7.38-7.42(m,2H),8.87(brs,1H),9.39(brs,1H)IR(KBr)3600-2800(br),1610,1585,1522,1495,1476,1448,1385,1292,1275,1199,1171,1136,985,948cm-1 |
I-864 | mp175-177℃1H NMR(DMSO-d6)δ2.44(s,12H),5.13(s,4H),6.77(s,2H),6.90-7.09(m,8H),7.33-7.52(m,8H),9.01(s,2H)IR(KBr)3600-2800(br),1582,1518,1491,1454,1384,1328,1270,1242,1191,1141,1123,1046,1006cm-1 |
I-865 | mp175-177℃1H NMR(CDCl3)δ2.52(s,12H),3.11(s,6H),5.17(s,4H),6.91(s,2H),7.11(d,J=8.4Hz,2H),7.36-7.52(m,12H),7.72(d,J=2.1Hz,2H)IR(KBr)3600-2800(br),1612,1520,1496,1455,1364,1348,1265,1184,1164,1117,1005,971cm-1 |
I-866 | mp180-182℃1H NMR(CDCl3)δ1.77(s,6H),1.81(s,6H),2.52(s,12H),3.22(s,6H),4.63(d,J=6.9Hz,2H),5.49-5.54(m,2H),6.90(s,2H),7.04(d,J=8.4Hz,2H),7.50(dd,J=2.1,8.4Hz,2H),7.04(d,J=2.1Hz,2H)IR(KBr)3600-2800(br),1520,1494,1365,1274,1186,1161,1113,996,973cm-1 |
I-867 | mp165-168℃1H NMR(DMSO-d6)δ1.72(s,6H),1.76(s,6H),2.45(s,12H),4.55(d,J=6.0Hz,4H),5.45-5.55(m,2H),6.77(s,2H),6.89-6.98(m,4H),7.03-7.07(m,2H),8.86(brs,2H)IR(KBr)3600-2800(br),1579,1519,1497,1476,1456,1384,1277,1238,1195,1142,1126,1050,994cm-1 |
I-868 | mp76-78℃1H NMR(CDCl3)δ3.47(s,3H),3.75(s,3H),3.94(s,3H),5.15(s,2H),5.68(s,1H),5.69(s,1H),5.92(s,1H),6.46(s,1H),6.93-7.15(m,5H),7.22(d,J=1.5Hz,1H),7.34-7.49(m,5H)IR(CHCl3)3528,1586,1520,1489,1461,1399,1287,1260,1110,1070,1010,907,819cm-1 |
I-869 | mp140-142℃1H NMR(CDCl3)δ2.65(s,3H),3.13(s,3H),3.25(s,3H),3.57(s,3H),3.78(s,3H),3.94(s,3H),5.19(s,2H),6.85(s,1H),7.13-7.19(m,2H),7.30-7.50(m,9H)IR(CHCl3)1598,1516,1480,1367,1266,1176,1115,1081,1012,969,918,867,808cm-1 |
I-870 | mp189-190℃1H NMR(CDCl3)δ1.76(d,J=0.9Hz,3H),1.81(s,3H),2.69(s,3H),3.24(s,3H),3.25(s,3H),3.58(s,3H),3.78(s,3H),3.94(s,3H),4.64(d,J=6.6Hz,2H),5.49(m,1H),6.85(s,1H),7.10(d,J=8.4Hz,1H),7.17(d.d,J=2.1,8.4Hz,1H),7.30-7.42(m,4H)IR(CHCl3)2932,1599,1516,1480,1367,1329,1266,1177,1115,1082,1032,1013,970,907,868,807cm-1 |
I-871 | mp187-190℃1H NMR(CDCl3)δ2.38(s,3H),2.64(s,3H),3.13(s,3H),3.25(s,3H),3.58(s,3H),3.78(s,3H),3.94(s,3H),5.14(s,2H),6.84(s,1H),7.13-7.24(m,4H),7.30-7.42(m,6H)IR(CHCl3) 2966,1598,1517,1480,1462,1368,1329,1267,1177,1116,1082,1032,970,907,867,808cm-1 |
I-872 | mp192-194℃1H NMR(CDCl3)δ1.15(t,J=6.9Hz,3H),1.76(s,3H),1.82(s,3H),2.59(s,3H),3.69(q,J=6.9Hz,2H),3.77(s,3H),4.61(d,J=6.9Hz,2H),4.99(s,1H),5.50(m,1H),5.70(s,1H),6.84(s,1H),6.88-6.97(m,3H),7.02(d,J=1.8Hz,1H),7.52-7.58(m,2H)IR(CHCl3)3536,2934,1609,1520,1482,1410,1365,1279,1243,1172,1128,1080,1029,972,952,872,833,812cm-1 |
I-873 | 1H NMR(CDCl3)δ3.46(s,3H),3.70(s,2H),3.74(s,3H),3.75(s,3H),5.15(s,2H),5.67(s,1H),5.90(s,1H),6.47(s,1H),6.96(d.d,J=8.4&1.8Hz,1H),7.03(d,J=8.4Hz,1H),7.09(d,J=1.8Hz,1H),7.33-7.44(m,7H),7.61(.d,J=8.4Hz,2H)IR(KBr)3536,3389,1732,1587,1519,1487,1438,1393,1249,1217,1166,1110,1069,1001cm-1 |
I-874 | 1H NMR(CDCl3)δ3.46(s,3H),3.74(s,5H),5.15(s,2H),5.68(s,1H),5.91(s,1H),6.47(s,1H),6.96(d.d,J=8.4&1.8Hz,1H),7.03(.d,J=8.4Hz,1H),7.09(.d,J=8.4Hz,1H),7.32-7.49(m,7H),7.62(d,J=8.1Hz,2H)IR(KBr)3381,1715,1698,1608,1681,1523,1485,1455,1396,1294,1235,1112,1072,1017cm-1 |
I-875 | 1H NMR(CDCl3)δ2.69(s,3H),3.13(s,3H),3.54(s,3H),3.70(s,2H),3.74(s,3H),3.77(s,3H),5.19(s,2H),6.88(s,1H),7.15(d,J=8.7Hz,1H),7.30-7.40(m,9H),7.59(.d,J=8.1Hz,2H)IR(KBr)1734,1721,1606,1481,1398,1361,1244,1175,1120,1078,1010cm-1 |
I-876 | 1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.73(s,3H),3.23(s,3H),3.54(s,3H),3.70(s,2H),3.74(s,3H),3.77(s,3H),4.64(d,J=6.9Hz,2H),5.46-5.55(m,1H),6.86(s,1H),7.09(d,J=8.4Hz,1H),7.35(d.d,J=8.4&2.1Hz,1H),7.37(d,J=8.1Hz,2H),7.39(d,J=2.1Hz,1H),7.59(d,J=8.1Hz,2H)1HNMR(CDCl3)δIR(KBr)3447,1735,1608,1522,1482,1355,1177,1117,1078,1013cm-1 |
I-877 | 1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.46(s,3H),3.74(s,5H),3H),4.62(d,J=6.9Hz,2H),5.46-5.58(m,1H),5.69(s,1H),5.89(s,1H),6.47(s,1H),6.96(s,2H),7.06(s,1H),7.38(d,J=8.4Hz,2H),7.62(d,J=8.4Hz,2H) |
I-878 | 1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.46(s,3H),3.70(s,2H),3.74(s,6H),4.62(d,J=6.9Hz,2H),5.46-5.58(m,1H),5.68(s,1H),5.88(s,1H),6.47(s,1H),6.96(s,2H),7.06(s,1H),7.37(d,J=8.4Hz,2H),7.61(d,J=8.4Hz,2H)IR(KBr)3527,3386,1734,1609,1586,1520,1487,1439,1396,1219,1167,1111,1068,1010cm-1 |
I-879 | mp136-139℃1H NMR(CDCl3)δ1.7(brs,1H),1.76(s,3H),1.81(s,3H),2.73(s,3H),3.23(s,3H),3.53(s,3H),3.78(s,3H),4.64(d,J=6.7Hz,2H),4.78(s,2H),5.49(t,J=6.8Hz,1H),6.87(s,1H),7.09(d,J=8.6Hz,1H),7.35(dd,J=8.6,2.1Hz,1H),7.40(d,J=2.1Hz,1H),7.47(d,J=8.1Hz,2H),7.64(d,J=8.1Hz,2H)IR(KBr)3553,3434,1481,1389,1363,1235,1175,1084,1011,972,806cm-1 |
I-880 | mp180-181℃1H NMR(CDCl3)δ1.70(brs,1H),1.76(s,3H),1.82(s,3H),3.46(s,3H),3.75(s,3H),4.62(d,J=6.9Hz,2H),4.77(s,2H),5.53(t,J=6.9Hz,1H),5.69(s,1H),5.89(s,1H),6.47(s,1H),6.94-6.96(m,2H),7.05-7.07(m,1H),7.46(d,J=8.1Hz,2H),7.65(d,J=8.4Hz,2H)IR(KBr)3509,3367,1522,1487,1461,1396,1289,1249,1213,1116,1071,1009,992,942,797,782cm-1 |
I-881 | mp122-123℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.34(t,J=6.5Hz,1H),3.22(s,3H),3.45(s,3H),3.73(s,3H),4.5(m,2H),4.64(d,J=6.6Hz,2H),5.56(t,J=6.6Hz,1H),6.84(s,1H),6.99-7.10(m,3H),7.39(d,J=8.7Hz,2H),7.71(d,J=8.7Hz,2H)IR(KBr)3579,1518,1471,1360,1261,1230,1148,1019,966,881,843cm-1 |
I-882 | mp156-158℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.49(t,J=6.6Hz,1H),3.44(s,3H),3.72(s,3H),4.49(br s,2H),4.63(d,J=6.7Hz,2H),5.04(s,1H),5.55(t,J=6.7Hz,1H),6.85s,1H),6.92(d,J=8.9Hz,2H),6.98-7.10(m,3H),7.53(d,J=8.9Hz,2H)IR(KBr)3433,3234,1609,1520,1472,1266,1227,994,836cm-1 |
I-883 | mp168-170℃1H NMR(CDCl3)δ2.50(t,J=6.5Hz,1H),3.44(s,3H),3.73(s,3H),4.49(brs,2H),4.78(d,J=6.1Hz,2H),5.06(s,1H),6.24(t,J=6.1Hz,1H),6.85(s,1H),6.93(d,J=8.6Hz,2H),6.97-7.13(m,3H),7.53(d,J=8.6Hz,2H)IR(KBr)3544,3412,3267,1613,1521,1475,1263,1229,1011,884,816cm-1 |
I-884 | mp153-154℃1H NMR(CDCl3)δ3.49(s,3H),3.77(s,3H),5.17(s,2H),5.76(brs,2H),6.45(s,1H),6.91-7.07(m,3H),7.26-7.45(m,5H),7.93(d,J=8.2Hz,2H),8.00(brs,1H),8.27(d,J=8.4Hz,2H)IR(KBr)3448,2962,2938,1738,1627,1604,1589,1519,1486,1319,1250,1153,1115,1071,1011cm-1 |
I-885 | mp81-82℃1H NMR(CDCl3)δ1.51(s,3H),1.54(s,3H),1.74(s,3H),1.77(s,3H),2.70(s,3H),3.24(s,3H),3.60(s,3H),3.78(s,3H),4.38(d,J=7.5Hz,2H),4.65(d,J=6.6Hz,2H),6.86(s,1H),7.06-7.11(m,3H),7.35-7.41(m,2H),7.52-7.57(m,1H)IR(KBr)3433,2938,1699,1618,1521,1481,1367,1209,1178,1115,1081,972,950,813,793cm-1 |
I-886 | mp208-209℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.71(s,3H),3.23(s,3H),3.60(s,3H),3.76(s,3H),4.64(d,J=7.2Hz,2H),5.49(t,J=8.7Hz,1H),6.85(s,1H),7.09(d,J=8.7Hz,1H),7.26-7.40(m,3H),7.52-7.58(m,1H),7.69-7.73(m,1H),8.02(brs,1H)IR(KBr)3357,2939,1736,1606,1523,1483,1398,1370,1294,1243,1179,1111,1079,965,827,814,795cm-1 |
I-887 | mp89-90℃1H NMR(CDCl3)δ2.34(s,3H),2.38(s,3H),2.64(s,3H),3.12(s,3H),3.53(s,3H),3.77(s,3H),4.92(s,2H),5.14(s,2H),6.83(s,1H),6.89(d,J=8.7Hz,2H),7.11-7.46(m,12H)IR(KBr)3434,2939,1699,1617,1520,1481,1367,1211,1178,1114,1081,952,813,794cm-1 |
I-888 | mp181-182℃1H NMR(CDCl3)δ2.38(s,3H),2.66(s,3H),3.12(s,3H),3.59(s,3H),3.76(s,3H),5.14(s,2H),6.85(s,1H),7.14-7.41(m,8H),7.52-7.58(m,1H),7.69-7.73(m,1H),8.02(brs,1H)IR(KBr)3348,3030,2940,1733,1607,1523,1482,1397,1366,1281,1242,1212,1179,1128,1112,1080,971,944,815,799cm-1 |
I-889 | mp155-157℃1H NMR(CDCl3)δ1.46(t,J=7.0Hz,3H),1.76(s,3H),1.82(s,3H),2.73(s,3H),3.23(s,3H),3.56(s,3H),3.74(s,3H),4.46(q,J=7.4Hz,2H),4.65(d,J=7.2Hz,2H),5.48-5.54(m,1H),6.69(s,1H),7.09(d,J=8.4Hz,2H),7.28-7.47(m,4H)IR(KBr)3434,2938,1716,1579,1477,1464,1409,1366,1241,1178,1124,1078,955,815,796cm-1 |
I-890 | mp82-83℃1H NMR(CDCl3)δ2.67(s,3H),3.13(s,3H),3.58(s,3H),3.80(s,3H),5.19(s,2H),6.84(s,1H),7.13-7.49(m,8H),7.89-7.96(m,2H),8.27(brs,1H),8.27-8.31(m,1H)IR(KBr)3447,3033,2940,1743,1521,1482,1367,1312,1272,1249,1178,1119,1080,957,817,799cm-1 |
I-891 | mp86-87℃1H NMR(CDCl3)δ2.68(s,3H),3.10(s,3H),3.15(s,3H),3.62(s,3H),3.81(s,3H),5.22(s,2H),6.85(s,1H),7.16-7.50(m,9H),7.88-7.94(m,2H)IR(KBr)3413,2938,1519,1483,1366,1313,1162,1119,1090,1079,957,812cm-1 |
I-892 | mp97-98℃1H NMR(CDCl3)δ1.53(s,3H),1.55(s,3H),1.76(s,3H),1.78(s,3H),3.63(s,3H),3.75(s,3H),4.26(d,J=7.4Hz,2H),4.62(d,J=6.8Hz,2H),5.65(br8,1H),5.72(brs,1H),6.84(s,1H),7.04-7.13(m,3H),7.35-7.43(m,2H),7.51-7.58(m,1H)IR(KBr)3453,3379,2973,2931,1719,1629,1529,1490,1406,1313,1288,1247,1193,1101,1072,1015,993,816,786cm-1 |
I-893 | mp89-90℃1H NMR(DMSO-d6)δ1.75(s,3H),1.78(s,3H),3.31(s,3H),3.62(s,3H),4.56(d,J=6.9Hz,2H),5.52(t,J=6.0Hz,1H),6.33(s,1H),6.34-6.47(m,2H),6.74(brs,2H),6.74-6.75(m,1H),6.87-6.91(m,1H),7.11-7.12(m,1H),7.32-7.34(m,1H),8.52(brs,1H),8.75(brs,1H)IR(KBr)3424,2933,2614,1719,1625,1585,1523,1488,1408,1287,1247,1125,1070,819,788cm-1 |
I-894 | mp167-168℃1H NMR(CDCl3)δ2.31(s,3H),2.38(s,3H)3.52(s,3H),3.76(s,3H),4.91(s,2H),5.13(s,2H),5.65(brs,1H),5.77(brs,1H),6.85(s,1H),6.84-6.93(m,2H),7.10-7.44(m,12H)IR(KBr)3425,2933,2614,1719,1625,1585,1522,1488,1408,1287,1247,1125cm-1 |
I-895 | mp93-94℃1H NMR(DMSO-d6)δ2.11(s,3H),3.34(s,3H),3.62(s,3H),5.10(s,2H),6.32(s,2H),6.41-6.49(m,2H),6.65(d,J=9.3Hz,1H),6.78(s,1H),6.95(d,J=8.7Hz,1H),7.09-7.14(m,1H),7.22(d,J=8.4Hz,2H),7.41(d,J=8.1Hz,2H),8.49(brs,1H),8.87(brs,1H)IR(KBr)3424,2932,1717,1626,1585,1523,1488,1409,1248,1125,1106,1070,811,793cm-1 |
I-896 | mp149-150℃1H NMR(DMSO-d6)δ1.72(s,3H),1.77(s,3H),3.32(s,3H),3.55(s,3H),3.76(s,6H),4.55(d,J=6.3Hz,2H),5.50(t,J=6.6Hz,1H),6.15(s,1H),6.68(d,J=2.1Hz,1H),6.91(d,J=8.7Hz,1H),7.30(s,2H),8.41(brs,1H),8.74(brs,1H)IR(KBr)3423,2936,1694,1578,1459,1410,1319,1229,1126,1067cm-1 |
I-897 | mp107-108℃1H NMR(CDCl3)δ2.70(s,3H),3.12(s,3H),3.55(s,3H),3.72(s,3H),3.78(s,6H),5.18(s,2H),6.65(s,1H),6.70(d,J=4.2Hz,1H),7.14(d,J=8.4Hz,1H),7.26-7.48(m,9H)IR(KBr)3434,2941,1517,1488,1366,1353,1261,1177,1102,1074,844,818,796cm-1 |
I-898 | 粉末1H NMR(CDCl3)δ1.63(s,3H),1.70(s,3H),3.48(s,3H),3.73-3.76(m,7H),3.87(s,3H),4.98(s,1H),5.24-5.32(m,2H),5.90(s,1H),6.47(s,1H),6.89-7.02(m,5H),7.51-7.57(m,2H)IR(KBr)3447,2930,1612,1523,1488,1455,1398,1230,1120,1080,1037,818,592cm-1 |
I-899 | mp171-173℃1H NMR(CDCl3)δ1.73(s,3H),1.76(s,3H),3.48(s,3H),3.73-3.76(m,5H),4.23(s,1H),4.92(s,1H),5.37-5.43(m,1H),5.84(s,1H),6.46(s,1H),6.70(d,J=8.1Hz,1H),6.86-7.01(m,5H),7.51-7.56(m,2H)IR(KBr)3392,2934,1612,1526,1489,1398,1222,1116,1075,829,590cm-1 |
I-900 | mp78-79℃1H NMR(CDCl3)δ2.14(s,3H),2.29(s,3H),2.36(s,3H),3.16(s,3H),3.20(s,3H),5.22(s,2H),7.10(s,1H),7.16(d,J=8.7Hz,1H),7.22-7.49(m,11H)IR(CHCl3)2939,1612,1516,1476,1415,1370,1291,1269,1174,1150,1119,1087,1018,971,954,873cm-1 |
I-901 | mp114-116℃1H NMR(CDCl3)δ1.08-1.14(m,6H),1.77(s,3H),1.81-1.82(d,J=0.6Hz,3H),2.53-2.65(m,4H),3.21(s,3H),3.23(s,3H),4.62-4.65(d,J=6.6Hz,2H),5.52(m,1H),7.04-7.13(m,2H),7.23-7.26(m,2H),7.32-7.42(m,5H)IR(CHCl3)2970,2934,2874,1674,1614,1572,1517,1487,1415,1370,1331,1288,1262,1172,1149,1109,971,937,872,849cm-1 |
I-902 | mp97-99℃1H NMR(CDCl3)δ1.07-1.14(m,6H),1.77(s,3H),1.83(s,3H),2.55-2.66(m,4H),4.61-4.64(d,J=6.6Hz,2H),5.06(s,1H),5.54(m,1H),5.77(s,1H),7.24-7.64(m,4H),6.97(d,J=2.1Hz,1H),7.10-7.12(d,J=5.7Hz,2H),7.23-7.26(m,2H)IR(CHCl3)3596,3537,2969,2933,27873,1675,1612,1586,1520,1489,1385,1327,1290,1257,1171,1125,998,903,877,836cm-1 |
I-903 | mp69-71℃1H NMR(CDCl3)δ1.78(s,3H),1.82(s,3H),2.15(s,3H),2.30(s,3H),2.43(s,3H),2.43(s,3H),3.21(s,3H),3.27(s,3H),4.64-4.67(d,J=6.9Hz,2H),5.50(s,2H),7.10-7.13(d,J=9.9Hz,2H),7.23-7.29(m,2H),7.34-7.42(m,5H)IR(CHCl3)2939,1612,1516,1476,1415,1370,1331,1290,1268,1174,1150,1119,1086,971,954,873cm-1 |
I-904 | mp125-127℃1H NMR(CDCl3)δ2.27(s,6H),3.91(s,3H),4.88(br,1H),5.20(s,2H),6.83-6.96(m,5H),7.12-7.13(d,J=4.5Hz,2H),7.22-7.50(m,7H)IR(CHCl3)3596,2957,2936,1611,1586,1522,1490,1464,1454,1326,1257,1172,1138,1033,835cm-1 |
I-905 | mp145-146℃1H NMR(CDCl3)δ2.26(s,3H),2.28(s,3H),3.20(s,3H),3.91(s,3H),5.21(s,2H),6.83(dd,J=8.1,2.1Hz,1H),6.91-6.96(m,2H),7.11(s,1H),7.15(s,1H),7.32-7.50(m,9H)IR(CHCl3)2938,16604,1584,1519,1488,1464,1454,1373,1330,1260,1175,1149,1033,1018,970,873,847cm-1 |
I-906 | mp132-134℃1H NMR(CDCl3)δ2.27(s,3H),2.87,(s,3H),3.91(s,3H),5.16(s,2H),5.21(s,2H),5.70(s,1H),6.82-6.86(m,2H),6.92-7.00(m,4H),7.13(s,2H),7,32-7.50(m,10H)IR(CHCl3)3542,2936,2871,1585,1519,1491,1454,1382,1322,1273,1175,1137,1014,897,877,857cm-1 |
I-907 | mp181-182℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.13(s,3H),2.30(s,3H),2.35(s,3H),4.61-4.64(d,J=6.9Hz,2H),5.37(s,1H),5.51(m,1H),5.78(s,1H),6.81(dd,J=8.1,2.1Hz,1H),6.86-6.97(m,3H),7.08(s,1H),7.19-7.22(m,2H),7.26(s,1H)IR(CHCl3)3595,3536,2936,1613,1587,1519,1479,1453,1359,1330,1279,1246,1173,1127,1085,1024,974,950,881,867cm-1 |
I-908 | mp167-168℃1H NMR(CDCl3)δ1.77-1.78(d,J=0.9Hz,3H),1.84(s,3H),2.08(s,3H),2.15(s,3H),4.63-4.65(d,J=6.9Hz,2H),4.82(s,1H),5.05(s,1H),5.55(m,1H),5.80(m,1H),6.74(s,1H),6.78(dd,J=8.4,2.1Hz,1H),6.87-6.95(m,3H),7.00(d,J=8.4Hz,1H),7.23-7.26(m,2H)IR(CHCl3)3594,3534,2923,2869,1675,1613,1584,1520,1488,1455,1399,1289,1247,1166,1127,1091,994,948,835cm-1 |
I-909 | mp170-172℃1H NMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),3.31(s,3H),3.63(s,3H),4.54(d,J=6.5Hz,2H),5.17(s,2H),5.49(t,J=6.5Hz,1H),6.36(s,1H),6.63(d,J=8.4Hz,2H),6.63(dd,J=8.4,2.1Hz,1H),6.72(d,J=2.1Hz,1H),6.88(d,J=8.4Hz,1H),7.31(d,J=8.4Hz,2H),8.40(s,1H),8.70(s,1H)IR(KBr)3416,3329,1614,1523,1489,1408,1242,1219,1115,1070,997,817,787cm-1 |
I-910 | mp207-209℃1H NMR(CDCl3)δ1.54(s,9H),2.69(s,3H),3.12(s,3H),3.52(s,3H),3.77(s,3H),5.18(s,2H),6.56(s,1H),6.85(s,1H),7.14(d,J=8.7Hz,1H),7.32-7.48(m,9H),7.57(d,J=8.7Hz,2H)IR(KBr)3373,1734,1525,1369,1227,1177,1158,1080,816,793cm-1 |
I-911 | mp214-216℃1H NMR(DMSO-d6)δ2.84(s,3H),3.33(s,3H),3.46(s,3H),3.75(s,3H),5.26(s,2H),5.30(s,2H),6.66(d,J=8.7Hz,2H),6.93(s,1H),7.24-7.45(m,8H),7.52(m,2H)IR(KBr)3468,3386,1604,1523,1482,1392,1361,1175,1085,815cm-1 |
I-912 | mp215-218℃1H NMR(CDCl3)δ2.67(s,3H),3.13(s,3H),3.53(s,3H),3.78(s,3H),5.19(s,2H),6.86(s,1H),7.15(d,J=8.4Hz,1H),7.32-7.48(m,7H),7.69(s,4H),8.02(brs,1H)IR(KBr) 3307,1733,1482,1393,1361,1284,1177,1084,1012,967,945,816cm-1 |
I-913 | mp203-205℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.71(s,3H),3.24(s,3H),3.54(s,3H),3.79(s,3H),4.64(d,J=6.8Hz,2H),5.50(t,J=6.8Hz,1H),6.86(s,1H),7.09(d,J=8.4Hz,1H),7.35(dd,J=8.4,2.0Hz,1H),7.39(d,J=2.0Hz,1H),7.69(s,4H),8.01(brs,1H)IR(KBr)3311,1735,1482,1393,1362,1177,1083,976,945,818cm-1 |
I-914 | mp105-107℃1H NMR(CDCl3)δ1.76(s,3H),1.80,(s,3H),2.27(s,3H),2.29(s,3H),3.20(s,3H),3.89(s,3H),4.63-4.65(d,J=6.6Hz,2H),5.57(m,1H),6.87-6.96(m,3H),7.12(s,1H),7.17(s,1H),7.33-7.43(m,4H)IR(CHCl3) 2937,2866,1604,1583,1519,1488,1464,1373,1331,1259,1175,1149,1035,970,873cm-1 |
I-915 | mp164-165℃1H NMR(CDCl3)δ1.75-1.76(d,J=0.6Hz,3H),1.79-1.80(d,J=0.9Hz,3H),2.27(s,3H),2.28(s,3H),3.89(s,3H),4.62-4.65(d,J=6.6Hz,2H),4.78(br,1H),5.57(m,1H),6.86-6.96(m,4H),7.12(s,1H),7.15(s,1H),7.22-7.27(m,3H)IR(CHCl3)3596,2936,2865,1676,1611,1584,1522,1490,1164,1385,1327,1257,1172,1138,1100,1035,996,952,896.,835cm-1 |
I-916 | mp172-173℃1H NMR(CDCl3)δ1.72(s,3H),1.77(s,6H),1.81(s,3H),2.70(s,3H),3.11(s,3H),3.24(s,3H),3.57(s,3H),3.80(s,3H),4.06-4.27(m,2H),4.64(d,J=7.2Hz,2H),5.37-5.50(m,2H),6.85(s,1H),7.10(d,J=8.6Hz,1H),7.32-7.39(m,2H),7.52(d,J=8.4Hz,1H),7.84(d,J=9.6Hz,1H),7.94(s,1H)IR(KBr)3434,1519,1482,1366,1346,1308,1178,1157,1120,1090,1078,957,805cm-1 |
I-917 | mp78-80℃1H NMR(CDCl3)δ3.47(s,3H),3.69(s,6H),3.80(s,6H),5.14(s,2H),5.66(brs,1H),5.76(brs,1H),6.30(s,1H),6.69(d,J=8.2Hz,2H),7.02(s,2H),7.14(s,1H),7.34-7.46(m,6H)IR(KBr)3443,2935,1614,1587,1517,1470,1250,1110,744cm-1 |
I-918 | mp83-84℃1H NMR(DMSO-d6)δ3.34(s,3H),3.72(s,3H),5.13(s,2H),5.72(brs,2H),6.41(s,1H),6.62-6.93(m,4H),7.32-7.61(m-7H),8.54(brs,1H),8.88(brs,1H)IR(KBr)3398,2936,1731,1633,1586,1521,1489,1455,1432,1402,1291,1216,1112,1071cm-1 |
I-919 | mp74-75℃1H NMR(CDCl3)δ2.02(s,6H),3.11(s,3H),3.21(s,3H),5.02(brs,1H),5.18(s,2H),6.96(s,1H),7.04-7.18(m,3H),7.37-7.59(m,9H)IR(KBr)3503,3032,2937,1513,1474,1365,1289,1197,1175,1149,1114,970,867,811cm-1 |
I-920 | mp78-79℃1H NMR(CDCl3)δ1.73(s,3H),1.78(s,6H),1.83(s,3H),3.11(s,3H),3.48(s,3H),3.77(s,3H),4.07-4.29(m,2H),4.64(d,J=6.8Hz,2H),5.41-5.55(m,2H),5.73(s,1H),5.82(s,1H),6.47(s,1H),6.94-7.05(m,3H),7.53(d,J=8.0Hz,1H),7.86(d,J=8.6Hz,1H),8.00(s,1H)IR(KBr)3449,2971,2935,1519,1489,1424,1338,1310,1226,1152,1117,1070,1059,773cm-1 |
I-921 | mp176-177℃1H NMR(CDCl3)δ2.10(s,3H),2.18(s,3H),2.47(s,3H),3.12(s,3H),3.23(s,3H),5.20(s,2H),7.09-7.21(m,3H),7.39-7.51(m,8H),7.60(d,J=8.4Hz,2H).IR(KBr)3433,3033,2937,1516,1470,1360,1291,1267,1176,1150,1119,976,867cm-1 |
I-922 | mp170-172℃1H NMR(DMSO-d6)δ3.36(s,3H),3.66(s,3H),4.22(br d,J=2.5Hz,2H),4.50(t,J=4.5Hz,1H),4.57(d,J=5.7Hz,2H),4.60(d,J=5.7Hz,2H),4.97(t,J=5.7Hz,2H),5.17(s,2H),5.23(t,J=5.7Hz,1H),6.93(s,1H),7.04(d,J=8.4Hz,1H),7.14(dd,J=8.4,2.3Hz,1H),7.28-7.37(m,2H),7.40-7.45(m,4H),7.49-7.53(m,2H),7.61(d,J=8.1Hz,2H)IR(KBr)3322,1462,1385,1228,1037,1006,750,700cm-1 |
I-923 | mp130-132℃1H NMR(CDCl3)δ1.55(s,9H),1.62(s,3H),2.30(s,12H),3.00(s,6H),6.73(brs,1H),6.78-6.82(m,2H),7.07-7.14(m,4H),7.24-7.27(m,2H),8.07-8.13(m,2H)IR(KBr)3600-2800(br),1732,1624,1610,1583,1530,1493,1366,1347,1320,1236,1154cm-1 |
I-924 | mp104-106℃1H NMR(CDCl3)δ2.27(s,3H),2.30(s,3H),3.00(s,6H),3.74(brs,2H),6.77-6.85(m,3H),6.96(dd,J=1.8,8.1Hz,1H),7.03(dd,J=2.1,12.0Hz,1H),7.09(s,1H),7.13(s,1H),7.24-7.29(m,2H)IR(KBr)3600-2800(br),1631,1608,1580,1530,1487,1436,1363,1233,1195cm-1 |
I-925 | mp100-102℃1H NMR(CDCl3)δ1.75(d,J=0.6Hz,3H),1.78(d,J=0.6Hz,3H),2.29(s,3H),2.30(s,3H),3.00(s,6H),3.77(d,J=6.6Hz,2H),3.87(brs,2H),5.37-5.40(m,1H),6.71-6.83(m,3H),7.00-7.03(m,2H),7.11(s,1H),7.13(s,1H),7.25-7.29(m,2H)IR(KBr)3600-2800(br),1623,1610,1529,1490,1441,1348,1328,1253,1229,1120,1065cm-1 |
I-926 | mp178-180℃1H NMR(CDCl3)δ2.27(s,3H),2.32(s,3H),3.01(s,6H),6.78-6.83(m,2H),7.10(s,1H),7.16(s,1H),7.18-7.28(m,4H),8.12(brs,1H),8.27-8.33(m,1H)IR(KBr)3600-2800(br),1709,1613,1532,1490,1356,1283,1229,1188,1167cm-1 |
I-927 | mp154-156℃1H NMR(CDCl3)δ1.94(d,J=1.2Hz,3H),2.26(d,J=1.2Hz,3H),2.27(s,3H),2.31(s,3H),3.00(s,6H),5.79-5.80(m,1H),6.78-6.82(m,3H),7.09-7.16(m,4H),7.16-7.24(m,2H),8.38-8.44(m,1H)IR(KBr)3600-2800(br),1681,1665,1643,1610,1528,1506,1487,1442,1359,1317,1237,1198,1159cm-1 |
I-928 | mp183-185℃1H NMR(CDCl3)δ1.44(t,J=7.5Hz,3H),2.27(s,3H),2.31(s,3H),3.16-3.23(m,2H),6.53(d,J=2.4Hz,1H),6.78-6.82(m,2H),7.09(s,1H),7.14-7.18(m,3H),7.24-7.27(m,3H),7.59-7.65(m,1H)IR(KBr)3600-2800(br),1607,1527,1491,1451,1436,1359,1336,1271,1222,1153,1110cm-1 |
I-929 | mp184-186℃1H NMR(CDCl3)δ2.26(s,3H),2.32(s,3H),3.01(s,6H),6.78-6.83(m,2H),7.10(s,1H),7,18(s,1H),7.23-7.27(m,1H),7.65(dd,J=1.8,8.1Hz,1H),7.70(d,J=2.1Hz,1H),8.19-8.24(m,1H)IR(KBr)3600-2800(br),1721,1612,1536,1490,1325,1282,1242,1197,1169,1123,1054cm-1 |
I-930 | mp212-215℃1H NMR(DMSO-d6)δ2.83(s,3H),3.43(s,3H),3.45(s,3H),3.52(s,3H),3.79(s,3H),4.87(s,2H),7.08(s,1H),7.21(d,J=8.4Hz,1H),7.27~7.32(m,2H),7.48(d,J=8.7Hz,2H),7.74(d,J=8.7Hz,2H)IR(Nujol)1731,1604,1519,1480,1237,1174,1081,1013,876,839,822,804cm-1 |
I-931 | mp166-168℃1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.67(d,J=9.0Hz,2H),6.45(s,1H),6.78(t,J=9.0Hz,1H),6.92(d,J=8.7Hz,2H),6.92(d,J=8.4Hz,1H),6.98(dd,J=8.4,2.1Hz,1H),7.09(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3399,1611,1588,1523,1488,1460,1224,1113,1070,1012,939,825,813,795cm-1 |
I-932 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.64~4.74(m,3H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.93(d,J=8.4,Hz,1H),6.97(dd,J=8.4,2.1Hz,1H),7.08(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3570,3461,3357,3180,1753,1616,1596,1524,1495,1408,1313,1287,1264,1240,1200,1114,1073,1011,906,825cm-1 |
I-933 | mp120-123℃1H NMR(CDCl3)δ1.69(s,3H),1.74(s,6H),1.80(s,3H),3.49(s,3H),6.68-3.75(m,5H),4.58(d,J=6.6Hz,2H),5.31-5.41(m,1H),5.50-5.56(m,1H),5.81(s,1H),6.46(s,1H),6.68-6.74(m,2H),6.85-6.93(m,3H),7.50-7.56(m,2H)IR(KBr)3460,2969,2929,1609,1523,1490,1398,1247,1117,1078,1013,824,778,708,589cm-1 |
I-934 | mp171-173℃1H NMR(CDCl3)δ1.75(s,3H),1.80(s,3H),3.47(s,3H),3.73(s,3H),3.81(s,2H),4.58(d,J=6.9Hz,2H),5.50-5.57(m,1H),5.82(s,1H),6.44(s,1H),6.77-6.94(m,5H),7.50-7.55(m,2H)IR(KBr)3382,3320,2929,1613,1523,1490,1405,1262,1221,1120,1067,1011,844,818,598cm-1 |
1-935 | mp220-221℃1H NMR(DMS0-d6)δ1.74(s,3H),1.77(s,3H),2.08(s,3H),3.30(s,3H),3.64(s,3H),4.64(d,J=7.2Hz,2H),5.48-5.54(m,1H),6.40(s,1H),6.80-6.87(m,2H),6.93-7.03(m,2H),7.42-7.46(m,2H),7.85(s,1H),8.58(s,1H),8.96(s,1H),9.56(s,1H)IR(KBr)3476,3400,3322,2935,1658,1610,1542,1520,1487,1270,1258,1225,1115,1010,825,596cm-1 |
I-936 | mp149-150℃1H NMR(CDCl3)δ1.48(s,3H),1.67(s,3H),1.76(8,3H),1.80(s,3H),3.63(s,3H),3.74(s,3H),4.27(d,J=7.5Hz,2H),4.63(d,J=6.6Hz,2H),5.01(s,1H),5.20-5.28(m,1H),5.52-5.60(m,1H),6.66(s,1H),6.91(d,J=8.7Hz,2H),7.01(t,J=8.7Hz,1H),7.10-7.22(m,2H),7.48(d,J=8.7Hz,2H)IR(KBr)3335,2936,1671,1614,1596,1522,1441,1403,1369,1265,1233,1111,1077,1008,945,832cm-1 |
I-937 | mp122-123℃1H NMR(CDCl3)δ3.44(s,3H),3.76(s,3H),4.77(d,J=6.3Hz,2H),5.05(s,1H),6.04(s,1H),6.24(t,J=6.3Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H)7.01(t,J=8.7Hz,1H),7.19-7.30(m,2H),7.53(d,J=8.7Hz,2H)IR(KBr)3582,3502,3237,2950,1614,1524,1490,1453,1403,1301,13267,1231,1112,1073,1019,881,827cm-1 |
I-938 | mp143-1444℃1H NMR(CDCl3)δ1.79(s,3H),1.84(s,3H),2.10(s,3H),2.17(s,3H),2.47(s,3H),3.23(s,3H),3.24(s,3H),4.66(d,J=6.6Hz,2H),5.20-5.55(m,1H),7.09-7.16(m,4H),7.40(d,J=8.7Hz,2H),7.60(d,J=8.1Hz,2H)IR(KBr)3433,2935,1513,1472,1366,1188,1178,1152,1117,974,857cm-1 |
I-939 | mp80-81℃1H NMR(CDCl3)δ3.47(s,3H),3.48(s,3H),3.68(s,3H),3.81(s,6H),4.79(s,2H),5.13(s,2H),5.14(s,2H),5.65(s,1H),5.75(s,1H),6.28(s,1H),6.69(s,2H),7.01(s,2H),7.14(s,1H),7.40-7.45(m,5H)IR(KBr)3433,2937,1720,1582,1508,1455,1407,1285,1239,1125,1069,1051,1011cm-1 |
I-940 | mp71-72℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.73(s,3H),3.21(s,3H),3.55(s,3H),3.72(s,3H),3.78(s,5H),4.63(d,J=6.8Hz,2H),5.46-5.52(m,1H),6.65(s,1H),6.70(d,J=3.8Hz,2H),7.07(d,J=8.4Hz,1H),7.34-7.46(m,3H)IR(KBr)3433,2938,1674,1609,1587,1518,14732,1365,1252,1178,1109,1077,971,945,815,796cm-1 |
I-941 | mp98-99℃1H NMR(CDCl3)δ1.74(s,3H),1.78(s,3H),3.50(s,3H),3.71(s,3H),3.72(d,J=8.1Hz,2H),5.35(t,J=7.2Hz,1H),5.64(s,1H),5.77(s,1H),6.43(s,1H),7.02-7.15(m,3H),7.32-7.41(m,2H),7.49-7.56(m,1H)IR(KBr)3408,2934,1627,1529,1491,1444,1405,1246,1175,1102,1069,822,783cm-1 |
I-942 | 1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.68(s,3H),2.73(s,3H),3.25(s,3H),3.60(s,3H),3.81(s,3H),4.65(d,J=6.3Hz,2H),5.44-5.53(m,1H),6.87(s,1H),7.10(d,J=8.7Hz,1H),7.30-7.47(m,3H),7.84(d.d,J=7.8&2.1Hz,1H),8.22(d,J=2.1Hz,1H)IR(KBr)1530,1480,1362,1272,1237,1179,1077cm-1 |
I-943 | 1H NMR(CDCl3)δ2.69(s,3H),3.12(s,3H),3.56(s,3H),3.77(s,3H),3.84(s,2H),5.18(s,2H),6.82(s,1H),6.84(d,J=8.1Hz,1H),7.14(d,J=8.4Hz,1H),7.21-7.50(m,9H)IR(KBr)3466,3377,1634,1583,1525,1488,1461,1400,1288,1245,1196,1105,1069cm-1 |
I-944 | 1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.49(s,3H),3.75(s,3H),4.61(d,J=6.6Hz,2H),5.48-5.57(m,1H),5.59-5.75(m,1H),5.88(s,1H),6.43(s,1H),6.83-7.07(m,4H),7.21-7.30(m,1H),7.35(d.d,J=12.3&1.8Hz,2H)IR(KBr)3465,3377,1634,1525,1488,1460,1400,1287,1245,1195,1105,1068cm-1 |
I-945 | 1HNMR(CDCl3)δ2.02(s,6H),2.15(s,3H),3.20(s,3H),5.20(s,3H),6.81-6.86(m,1H),6.93(d.d,J=10.7&2.1Hz,1H),6.97(s,1H),7.04-7.12(m,1H),7.31-7.52(m,9H)IR(KBr)1513,1468,1362,1295,1264,1227,1193,1171,1151,1003,965cm-1 |
I-946 | 1H NMR(CDCl3)δ2.02(s,6H),2.15(s,3H),3.20(s,3H),5.14(d,J=3.9Hz,1H),6.81-6.86(m,1H),6.91(d.d,J=10.1&2.1Hz,1H),6.97(s,1H),7.04-7.12(m,1H),7.30-7.42(m,4H)IR(KBr)3414,1624,1595,1518,1473,1360,1294,1170,1144,112,1104,1016cm-1 |
I-947 | 1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.02(s,6H),2.16(s,3H),3.20(s,3H),4.64(d,J=6.6Hz,2H),5.53-5.61(m,1H),6.82-7.09(m,4H),7.33(d,J=9.0Hz,2H),7.39(d,J=9.0Hz,2H)IR(KBr)1514,1468,1376,1294,1262,1175,1152,992,968cm-1 |
I-948 | 1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.02(s,6H),2.17(s,3H),4.64(d,J=6.6Hz,2H),4.81(s,1H),5.52-5.60(m,1H),6.82-7.08(m,6H),7.22(d,J=8.7Hz,2H)IR(KBr)3568,3417,1613,1517,1471,1287,1261,1230,1192,1132,1102,1001cm-1 |
I-949 | 1H NMR(CDCl3)δ3.02(s,6H),3.46(s,3H),3.75(s,3H),5.18(s,2H),6.03(s,1H),6.47(s,1H),6.82(d,J=8.7Hz,2H),7.03-7.51(m,8H),7.55(d,J=8.7Hz,2H)IR(KBr)3502,1604,1527,1488,1359,1267,1233,1198,1110,1070cm-1 |
I-950 | 1H NMR(CDCl3)δ2.60(s,3H),3.03(s,6H),3.54(s,3H),3.76(s,3H),5.21(s,2H),6.80(d,J=8.7Hz,2H),6.86(s,1H),7.03-7.49(m,8H),7.54(d,J=8.7Hz,2H)IR(KBr)1602,1530,1483,1444,1395,1366,1233,1179,1078,1015cm-1 |
I-951 | 1H NMR(CDCl3)δ2.76(s,3H),3.02(s,6H),3.54(s,3H),3.76(s,3H),5.28(s,1H),6.81(d,J=9.0Hz,2H),6.86(s,1H),7.04-7.23(m,3H),7.54(d,J=9.0Hz,2H)IR(KBr)3375,1607,1530,1483,1395,1346,1292,1228,1163,1077,1009cm-1 |
I-952 | 1H NMR(CDCl3)δ1.78(s,3H),1.80(s,3H),2.71(s,3H),3.02(s,6H),3.55(s,3H),3.76(s,3H),4.63(d,J=6.9Hz,2H),5.49-5.57(m,1H),6.82(d,J=8.7Hz,2H),6.86(s,1H),7.01-7.23(m,3H),7.54(d,J=8.7Hz,2H)IR(KBr)1602,1531,1484,1389,1369,1258,1235,1197,1176,1084cm-1 |
I-953 | 1H NMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.02(s,6H),3.47(s,3H),3.75(s,3H),4.63(d,J=6.9Hz,2H),5.51-5.60(m,1H),6.03(s,1H),6.47(s,1H),6.82(d,J=8.7Hz,2H),6.99-7.08(m,1H),7.16-7.29(m,2H),7.55(d,J=8.7Hz,2H)IR(KBr)3498,1604,1528,1488,1360,1266,1234,1198,1110,1067cm-1 |
I-954 | 1H NMR(CDCl3)δ3.02(s,6H),3.47(s,3H),3.75(s,3H),5.14(s,1H),6.03(s,1H),6.47(s,1H),6.82(d,J=9.0Hz,2H),7.02-7.09(m,1H),7.15-7.29(m,2H),7.55(d,J=9.0Hz,2H)IR(KBr)3492,3383,1607,1529,1488,1397,1223,1103,1065,1006cm-1 |
I-955 | 1H NMR(CDCl3)δ2.01(s,6H),2.17(s,3H),4.75(s,1H),5.19(s,2H),6.83-7.15(m,7H),7.30-7.53(m,6H)IR(KBr)3542,1607,1579,1513,1469,1263,1126,1107,1015cm-1 |
I-956 | 1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.66(s,3H),3.50(s,3H),3.77(s,3H),4.62(d,J=6.4Hz,2H),5.48-5.56(m,1H),5.71(s,1H),5.81(s,1H),5.47(s,1H),6.90-7.00(m,2H),7.04(d,J=1.8Hz,1H),7.42(d,J=7.8Hz,2H),7.82(d.d,J=7.8&1.8Hz,1H),8.26(d,J=1.5Hz,1H)IR(KBr)3520,3419,1585,1529,1506,1344,1313,1290,1251,1226,1118,1079cm-1 |
I-957 | mp123-126℃1H NMR(CDCl3)δ1.75(s,3H),1.78(d,J=0.9Hz,3H),3.47(s,3H),3.75(s,3H),3.87(s,3H),3.88(s,3H),4.63(d,J=6.6Hz,2H),5.57(m,1H),5.92(s,1H),6.47(s,1H),6.95-7.40(m,5H),7.56-7.62(m,2H)IR(CHCl3)3510,2934,1608,1519,1489,1461,1394,1285,1243,1175,1115,1075,1034,1008,926,823cm-1 |
I-958 | mp163-164℃1H NMR(CDCl3)δ1.75(s,3H),1.78(s,3H),3.61(s,3H),3.65(s,3H),3.75(s,3H),3.88(s,3H),4.64(d,J=6.6Hz,2H),4.99(s,1H),5.58(m,1H),6.68(s,1H),6.88-6.98(m,5H),7.46-7.52(m,2H)IR(CHCl3)3592,2934,1610,1517,1461,1387,1237,1171,1136,1111,1084,1036,1012,830cm-1 |
I-959 | mp142-146℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.47(s,3H),3.75(s,3H),3.94(s,3H),4.61(d,J=6.6Hz,2H),5.53(m,1H),5.69(s,1H),5.70(s,1H),5.91(s,1H),6.46(s,1H),6.94-7.26(m,6H)IR(CHCl3)3526,2930,1585,1520,1489,1460,1399,1287,1260,1110,1070,1010,819cm-1 |
I-960 | mp141-145℃1H NMR(CDCl3)δ2.39(s,3H),3.47(s,3H),3.94(s,3H),5.10(s,2H),5.68(s,1H),5.69(s,1H),5.92(s,1H),6.46(s,1H),6.93-7.38(m,6H)IR(CHCl3)3528,1585,1519,1489,1460,1399,1260,1110,1070,1009,863cm-1 |
I-961 | mp152-154℃1H NMR(CDCl3)δ2.26(s,3H),4.79(br,1H),5.19(s,2H),6.87-6.90(m,2H),7.03-7.15(m,4H),7.22-7.26(m,2H),7.34-7.50(m,6H)IR(CHCl3)3596,2925,2869,1612,1581,1523,1490,1455,1383,1313,1298,1259,1171,1125,1100,1012,956,877,836cm-1 |
I-962 | mp150-151℃1H NMR(CDCl3)δ2.28(s,3H),3.90(s,3H),4.77-4.79(d,J=6.0Hz,2H),6.26(d,J=6.0Hz,1H),6.88-6.91(m,5H),7.13-7.14(d,J=2.7Hz,2H),7.24-7.27(m,2H)IR(CHCl3)3596,2958,1732 1612,1587,1522,1490,1464,1325,1257,1172,1139,1100,1032,886,835cm-1 |
I-963 | mp93-94℃1H NMR(CDCl3)δ2.27(s,3H),4.76-4.79(d,J=6.0Hz,2H),5.12(br,1H),6.24(t,J=6.0Hz,1H),6.88-7.15(m,7H),7.22-7.26(m,2H)IR(CHCl3)3596,2925,2867,1613,1583,1523,1490,1458,1424,1388,1258,1171,1126,1100,1022,956,886,836cm-1 |
I-964 | 泡沫1H NMR(CDCl3)δ3.47(s,3H),3.74(s,3H),5.06(s,1H),5.15(s,2H),5.70(s,1H),5.94(s,1H),6.46(s,1H),6.81-7.50(m,12H)IR(CHCl3)3534,1609,1587,1518,1504,1482,1463,1455,1407,1322,1290,1249,1200,1112,1072,1011cm-1 |
I-965 | 泡沫1H NMR(CDCl3)δ3.61(s,3H),3.75(s,3H),5.16(s,2H),5.72(s,2H),6.46(s,1H),6.83(s,1H),6.94(dd,J=2.0,8.4Hz,1H),7.00-7.12(m,4H),7.29-7.50(m,7H)IR(CHCl3)3531,1587,1516,1498,1482,1462,1455,1410,1362,1308,1288,1248,1202,1121,1092,1070,1006cm-1 |
I-966 | mp174-175℃1H NMR(CDCl3)δ2.28(s,3H),3.38(s,3H),3.71(s,3H),5.16(s,2H),5.68(s,1H),5.88(s,1H),6.30(s,1H),6.98(dd,J=1.8,8.4Hz,1H),7.04(d,J=8.4Hz,1H),7.11(d,J=1.8Hz,1H),7.22-7.49(m,9H)IR(KBr)3516,3398,1587,1516,1500,1484,1453,1412,1306,1285,1247,1231,1202,1126,1101,1072,1019,769,737cm-1 |
I-967 | mp103-104℃1H NMR(CDCl3)δ2.26(s,6H),4.61-4.78(m,3H),4.84(s,1H),6.84-6.92(m,2H),6.97-7.16(m,5H),7.21-7.27(m,2H)IR(KBr)3409,1742,1523,1489,1315,1295,1259,1231,1206,1193,1124,1001,834,815cm-1 |
I-968 | mp90-91℃1H NMR(CDCl3)δ1.77(s,6H),1.82(d,J=0.9Hz,6H),2.27(s,6H),4.56(d,J=6.6Hz,2H),5.13(d,J=6.6Hz,2H),5.49-5.60(m,2H),6.94-7.00(m,2H),7.01-7.14(m,5H),7.25-7.31(m,2H)IR(KBr)1608,1522,1488,1378,1299,1288,1273,1259,1242,1196,1176,1014,831,811,776cm-1 |
I-969 | mp200-203℃1H NMR(CDCl3)δ2.00(s,3H),2.25(s,3H),3.46(s,3H),3.73(s,3H),3.83(s,3H),5.25(s,1H),6.01-6.03(m,1H),6.06(s,1H),6.45(s,1H),6.86-6.90(m,2H),7.04-7.14(m,3H),7.47-7.52(m,2H)IR(KBr)3433,2937,1721,1651,1523,1489,1398,1264,1225,1136,1071,1035,927,823,530cm-1 |
I-970 | mp157-160℃1H NMR(CDCl3)δ1.74(s,3H),1.80(s,3H),2.86(s,3H),3.49(s,3H),3.75(s,3H),4.57(d,J=6.6Hz,2H),5.08(s,1H),5.50-5.57(m,1H),5.82(s,1H),6.46(s,1H),6.66(d,J=2.1Hz,1H),6.73(dd,J=2.1,8.1Hz,1H),6.86-6.94(m,3H),7.50-7.56(m,2H)IR(KBr)3392,2934,1611,1523,1490,1397,1242,1216,1112,1074,1002,592cm-1 |
I-971 | mp153-155℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.10(s,3H),3.20(s,3H),3.21(s,3H),3.36(s,3H),3.71(s,3H),4.63(d,J=6.9Hz,2H),5.52(t,J=6.9Hz,1H),6.73(s,1H),7.06(d,J=8.4Hz,1H),7.14(dd,J=8.4,2.1Hz,1H),7.23(d,J=2.1Hz,1H),7.36(d,J=8.9Hz,2H),7.69(d,J=8.9Hz,2H)IR(KBr)1515,1474,1365,1229,1175,1151,1096,973,870,810cm-1 |
I-972 | 无定形1H NMR(CRCl3)δ1.77(s,3H),1.82(s,3H),2.43(s,3H),3.44(s,3H),3.71(s,3H),4.49(d,J=9.9Hz,2H),4.62(d,J=6.6Hz,2H),4.72(d,J=7.2Hz,2H),5.53(t,J=6.6Hz,1H),6.86(s,1H),6.96(d,J=8.7Hz,1H),7.21-7.30(m,4H),7.54(d,J=8.1Hz,2H)IR(KBr)3599,1463,1386,1081,1007cm-1 |
I-973 | mp83-86℃1H NMR(DMSO-d6)δ1.74(s,3H),1.77(s,3H),3.36(s,3H),3.65(s,3H),4.23(d,J=23.1Hz,2H),4.48(t,J=4.4Hz,1H),4.52(d,J=5.4Hz,2H),4.52-4.60(m,4H),4.89(t,J=5.6Hz,1H),5.22(t,J=5.9Hz,1H),5.48(t,J=6.6Hz,1H),6.92(s,1H),6.96(d,J=8.6Hz,1H),7.12(dd,J=8.6,1.5Hz,1H),7.26(d,J=1.5Hz,1H),7.42(d,J=8.0Hz,2H),7.61(d,J=8.0Hz,2H)IR(KBr)3399,1464,1386,1230,1005cm-1 |
I-974 | mp177-179℃1H NMR(CDCl3)δ1.31(d,J=6.9Hz,6H),2.70(s,3H),2.98(sept,J=6.9Hz,1H),3.12(s,3H),3.54(s,3H),3.76(s,3H),5.19(s,2H),6.87(s,1H),7.15(d,J=8.4Hz,1H),7.30-7.49(m,9H),7.54(d,J=7.8Hz,2H)IR(KBr)1512,1480,1369,1176,1084,1014,813,798cm-1 |
I-975 | mp180-182℃1H NMR(CDCl3)δ1.31(d,J=6.6Hz,6H),1.76(s,3H),1.81(s,3H),2.74(s,3H),2.98(sept,J=6.6Hz,1H),3.22(s,3H),3.54(s,3H),3.77(s,3H),4.63(d,J=6.7Hz,2H),5.49(t,J=6.7Hz,1H),6.87(s,1H),7.08(d,J=8.4Hz,1H),7.31(d,J=8.1Hz,2H),7.35(dd,J=8.4,2.1Hz,1H),7.40(d,J=2.1Hz,1H),7.54(d,J=8.1Hz,2H)IR(KBr)1520,1481,1366,1177,1083,1012,975,944,815,797cm-1 |
I-976 | mp125-126℃1H NMR(CDCl3)δ1.31(d,J=6.9Hz,6H),1.76(s,3H),1.82(s,3H),2.97(sept,J=6.9Hz,1H),3.46(s,3H),3.74(s,3H),4.61(d,J=7.1Hz,2H),5.53(t,J=7.1Hz,1H),5.68(s,1H),5.91(s,1H),6.48(s,1H),6.95-6.96(m,2H),7.06-7.07(m,1H),7.31(d,J=8.0Hz,2H),7.57(d,J=8.0Hz,2H)IR(KBr)cm-1 |
I-977 | 泡沫1H NMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.20(s,3H),3.57(s,3H),3.79(s,3H),5.19(s,2H),6.86(s,1H),7.15(d,J=8.7Hz,1H),7.31-7.62(m,11H)IR(CHCl3)1517,1475,1371,1227,1219,1176,1117,1081,968,925,856,821cm-1 |
I-978 | 泡沫1H NMR(CDCl3)δ2.65(s,3H),2.94(s,3H),3.14(s,3H),3.59(s,3H),3.76(s,3H),5.19(s,2H),6.86(s,1H),7.16(d,J=8.7Hz,1H),7.33-7.57(m,11H)IR(CHCl3)1517,1477,1398,1370,1268,1233,1216,1177,1159,1079,972,894,856,818cm-1 |
I-979 | 泡沫1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.69(s,3H),2.94(s,3H),3.25(s,3H),3.60(s,3H),3.76(s,3H),4.64(d,J=6.9Hz,2H),5.50(m,1H),6.86(s,1H),7.10(d,J=8.4Hz,1H),7.34-7.57(m,11H)IR(CHCl3)1517,1476,1398,1369,1234,1178,1159,1105,1079,972,895,854,814,801cm-1 |
I-980 | 泡沫1H NMR(CDCl3)δ1.76(d,J=0.9Hz,3H),1.81(d,J=0.9Hz,3H),2.71(s,3H),3.20(s,3H),3.24(s,3H),3.57(s,3H),3.79(s,3H),4.64(d,J=6.6Hz,2H),5.49(m,1H),6.86(s,1H),7.09(d,J=8.7Hz,1H),7.31-7.40(m,3H),7.48-7.55(m,3H)IR(CHCl3)1517,1474,1365,1269,1236,1177,1140,1116,1078,964,923,854,814cm-1 |
I-981 | mp122-123℃1H NMR(CDCl3)δ1.77(s,3H),1.82(d,J=0.4Hz,3H),3.62(s,3H),3.75(s,3H),4.63(d,J=6.6Hz,2H),5.53(m,1H),5.70(s,1H),5.73(s,1H),6.46(s,1H),6.86(s,1H),6.89-7.13(m,4H),7.29-7.46(m,3H)IR(KBr)3366,1587,1496,1482,1462,1449,1408,1371,1313,1290,1245,1210,1126,1093,1073,1001,783,770cm-1 |
I-982 | mp171-172℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.48(s,3H),3.74(s,3H),4.61(d,J=6.9Hz,2H),4.91(s,1H),5.53(m,1H),5.70(s,1H),5.91(s,1H),6.46(s,1H),6.86(m,1H),6.91-7.02(m,2H),7.06(m,1H),7.13(m,1H),7.21(m,1H),7.32(m,1H)IR(KBr)3368,1585,1519,1507,1484,1460,1450,1403,1294,1255,1237,1206,1110,1072,1006,789,766cm-1 |
I-983 | mp92.5-93℃1H NMR(CDCl3)δ1.77(s,3H),1.83(d,J=0.9Hz,3H),2.26(s,3H),2.27(s,3H),4.63(d,J=6.9Hz,2H),5.13(d,J=3.9Hz,1H),5.55(m,1H),6.98-7.14(m,8H)IR(CHCl3)3578,2922,1618,1522,1490,1383,1282,1120,979,873,824cm-1 |
I-984 | mp89-95℃1H NMR(CDCl3)δ1.77(s,6H),1.81(d,J=0.9Hz,6H),2.27(s,6H),4.63(d,J=6.6Hz,4H),5.55(m,2H),6.98-7.14(m,8H)IR(CHCl3) 2930,1576,1520,1490,1382,1296,1270,1127,987,874cm-1 |
I-985 | mp74-75℃1H NMR(CDCl3)δ2.16(s,3H),2.69(s,3H),3.14(s,3H),3.20(s,3H),3.56(s,3H),5.20(s,2H),7.16-7.49(m,11H),7.65-7.68(m,2H)IR(CHCl3)2939,1732,1613,1518,1478,1454,1415,1371,1331,1292,1268,1176,1150,1118,1088,1010,969,950,872cm-1 |
I-986 | mp50-52℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.16(s,3H),2.74(s,3H),3.20(s,3H),3.24(s,3H),3.57(s,3H),4.64-4.66(d,J=6.3Hz,2H),5.50(m,1H),7.10-7.39(m,6H),7.66-7.68(m,2H)IR(CHCl3)2938,1613,1518,1477,1370,1331,1290,1267,1176,1150,1117,1088,970,949,871cm-1 |
I-987 | 1H NMR(CDCl3)δ1.59-1.60(d,J=0.6Hz,3H),1.70-1.71(d,J=0.9Hz,3H),2.26(s,3H),2.28(s,3H),2.36(m,1H),2.77(m,1H),3.20(s,3H),3.23(s,3H),5.24(m,1H),7.12(s,1H),7.15(s,1H),7.23-7.25(m,1H),7.33-7.42(m,6H) |
I-988 | mp159-161℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.12(s,3H),3.48(s,3H),4.61-4.64(d,J=6.6Hz,2H),4.75(br,1H),5.54(m,1H),5.69(s,1H),5.73(s,1H),6.77-6.98(m,6H),7.51-7.54(m,2H)IR(CHCl3)3595,3529,2937,1613,15787,1522,1489,1455,1401,1310,1289,1173,1127,1095,1009,939,835cm-1 |
I-989 | mp126-128℃1H NMR(CDCl3)δ2.25(s,3H),3 78(s,3H),5.16(s,2H),5.75(br,1H),6.83-6.89(m,4H),6.98-7.00(m,2H),7.17(s,1H),7.40-7.47(m,7H)IR(CHCl3)3596,3543,2937,1610,1588,1523,1493,1465,1455,1388,1328,1315,1262,1173,1126,1038,1012,835cm-1 |
I-990 | mp87-90℃1H NMR(CDCl3)δ1.59-1.60(d,J=0.6Hz,3H),1.72-1.73(d,J=0.9Hz,3H),2.26(s,3H),2.28(s,3H),2.34-2.37(m,2H),2.66-2.71(m,2H),4.84-4.86(br,2H),5.28(m,1H),6.79(d,J=1.5Hz,1H),6.86-6.89(m,3H),7.11-7.17(m,3H),7.23-7.26(m,2H)IR(CHCl3)3598,2925,2859,1612,1569,1521,1488,1450,1425,1414,1328,1257,1171,1101,958,836cm-1 |
I-991 | mp174-176℃1H NMR(CDCl3)δ2.26(s,3H),3.13(s,3H),3.18(s,3H),3.80(s,3H),5.19(s,2H),6.84(s,1H),7.13(d,J=8.4Hz,1H),7.18(s,1H),7.28-7.50(m,9H),7.59-7.62(m,2H)IR(CHCl3)2940,1732,1613,1520,1490,1465,1455,1415,1371,1331,1291,1260,1173,1149,1111,1038,1018,1003,971,872,813cm-1 |
I-992 | mp135-137℃1H NMR(CDCl3)δ1.77-1.78(d,J=0.9Hz,3H),1.82-1.83(d,J=0.6Hz,3H),2.26(s,3H),3.18(s,3H),3.24(s,3H),3.80(s,3H),4.64(d,J=6.6Hz,2H),5.52(m,1H),6.84(s,1H),7.07(d,J=8.7Hz,1H),7.18(s,1H),7.25-7.35(m,4H),7.59-7.62(m,2H)IR(CHCl3)3596,3539,2937,1610,1587,1523,1492,1464,1454,1388,1328,1315,1292,1261,1173,1126,1038,996,834cm-1 |
I-993 | mp131-133℃1H NMR(CDCl3)δ1.77(s,3H),1.83(s,3H),2.26(s,3H),3.78(s,3H),4.61-4.64(d,J=6.9Hz,2H),5.17(br,1H),5.35(m,1H),5.78(br,1H),6.83-6.99(m,6H),7.17(s,1H),7.44-7.47(m,2H)IR(CHCl3)3596,3539,2937,1610,1587,1523,1492,1464,1454,1388,1328,131,1292,1261,1173,1126,1038,996,834cm-1 |
I-994 | mp127-130℃1H NMR(CDCl3)δ1.73(d,J=0.9Hz,3H),1.76(d,J=0.9Hz,3H),2.99(s,6H),3.73-3.76(m,2H),3.78(s,6H),3.88(s,3H),5.37-5.40(m,1H),5.83(d,J=7.8Hz,1H),6.78-6.84(m,2H),6.95(s,1H),6.96(s,1H),7.06-7.12(m,2H),7.48-7.53(m,2H) |
I-995 | mp91-93℃1H NMR(CDCl3)δ1.78(s,3H),1.84(s,3H),2.02(s,6H),4.63(d,J=6.4Hz,2H),5.07(s,1H),5.15(s,1H),5.55(t,J=7.0Hz,1H),6.63(dd,J=2.0,8.2Hz,1H),6.77(d,J=2.0Hz,1H),6.93-6.99(m,4H),7.39(d,J=8.6Hz,2H)IR(KBr)3423,2921,1611,1518,1474,1282,1244,1205,1125,1089,995,837,815,785cm-1 |
I-996 | mp185-186℃1H NMR(CDCl3)δ1.32(t,J=7.5Hz,3H),2.71(q,J=7.5Hz,2H),3.46(s,3H),3.76(s,3H),5.15(s,2H),5.69(s,1H),5.89(s,1H),6.94-7.08(m,3H),7.37-7.46(m,5H),7.54-7.59(m,2H),7.82(brs,1H),7.93(d,J=8.1Hz,1H)IR(KBr)3504,3269,2968,2936,1708,1532,1518,1487,1311,1286,1193,1121,1071,1014cm-1 |
I-997 | mp77-78℃1H NMR(CDCl3)δ1.73(s,3H),1.77(s,3H),1.82(s,3H),2.70(s,3H),3.25(s,3H),3.55(s,3H),3.82(s,3H),4.65(d,J=6.9Hz,2H),4.94(d,J=7.5Hz,2H),5.31(t,J=8.7Hz,1H),5.50(t,J=6.6Hz,1H),6.87(s,1H),7.10(d,J=8.4Hz,1H),7.28-7.39(m,3H),7.87(d,J=8.1Hz,1H),7.99(s,1H)IR(KBr)3431,2939,1702,1518,1483,1368,1308,1204,1177,1121,1092,1079,957,804cm-1 |
I-998 | mp144-145℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.48(s,3H),3.69(s,3H),3.80(s,6H),4.61(d,J=6.9Hz,2H),5.51(t,J=4.8Hz,1H),5.66(brs,1H),5.76(brs,1H),6.30(s,1H),6.69(d,J=8.1Hz,2H),6.93-7.01(m,2H),7.11(d,J=2.1Hz,1H),7.31-7.37(m,1H)IR(KBr)3476,2936,1589,1517,1500,1472,1408,1288,1249,1111cm-1 |
I-999 | mp82-83℃1H NMR(CDCl3)δ2.71(s,3H),3.15(s,3H),3.48(s,3H),3.56(s,3H),3.72(s,3H),3.80(s,6H),4.66(s,2H),4.79(s,2H),5.19(s,2H),6.69(s,1H),7.14-7.17(m,1H),7.36-7.49(m,8H)IR(KBr)3434,2939,1719,1613,1581,1508,1463,1396,1365,1294,1272,1238,1177,1122,1078,814cm-1 |
I-1000 | mp85-86℃1H NMR(CDCl3)δ1.31(t,J=7.5Hz,3H),2.66(s,3H),2.71(q,J=7.6Hz,2H),3.13(s,3H),3.55(s,3H),3.78(s,3H),5.19(s,2H),6.85(s,1H),7.15(d,J=8.8Hz,1H),7.33-7.59(m,4H),7.85(brs,1H),7.94(d,J=8.4Hz,1H)IR(KBr)3432,2939,1727,1519,1480,1365,1237,1165,1079,959,803cm-1 |
I-1001 | mp105-106℃1H NMR(CDCl3)δ1.76(s,6H),1.79(s,3H),1.82(s,3H),3.49(s,3H),3.75(s,3H),3.81(d,J=6.6Hz,2H),4.62(d,J=7.2Hz,2H),5.37(t,J=6.3 Hz,1H),5.53(t,J=6.9Hz,1H),5.68(brs,1H),5.87(brs,1H),6.82(d,J=8.4Hz,1H),6.95(s,2H),7.05(s,1H),7.26(s,1H),7.69(dd,J=2.1,8.4Hz,1H),7.75(brs,1H)IR(KBr) 3459,2934,1622,1582,1525,1493,1467,1327,1240,1139,1113,1070,817cm-1 |
I-1002 | mp89-91℃1HNMR(CDCl3)δ2.70(s,3H),3.12(s,3H),3.55(s,3H),3.71(s,3H),3.79(s,6H),4.77(s,2H),5.18(s,2H),5.69(s,2H),7.14(d,J=8.8Hz,1H),7.38-7.52(m,8H)IR(KBr)3440,2939,1721,1612,1581,1508,1463,1395,1364,1238,1178,1120,1078,962,814,523cm-1 |
I-1003 | mp196-197℃1H NMR(CDCl3)δ2.26(s,3H),3.48(s,3H),3.76(s,3H),5.16(s,2H),5.69(brs,1H),5.83(brs,1H),6.44(s,1H),6.93-7.05(m,4H),7.26-7.45(m,6H),7.84(d,J=8.1Hz,1H),7.92(s,1H),8.29(brs,1H)IR(KBr)3407,2934,1672,1589,1524,1459,1425,1400,1316,1288,1213,1119,1057,1006,745cm-1 |
I-1004 | mp80-81℃1H NMR(CDCl3)δ1.29(t,J=7.5Hz,3H),1.72(s,3H),1.76(s,6H),1.81(s,3H),2.70(s,3H),2.71(q,J=7.5Hz,2H),3.24(s,3H),3.50(s,3H),3.81(s,3H),4.64(d,J=6.3Hz,2H),4.72-4.76(m,2H),5.31(t,J=6.9Hz,1H),5.50(t,J=6.3Hz,1H),6.87(s,1H),7.08-7.12(m,2H),7.34-7.41(m,3H),7.61(s,1H)IR(KBr) 3434,2974,2938,1694,1517,1480,1366,1237,1202,1177,1080,972,807,523cm-1 |
I-1005 | mp157-158℃1H NMR(CDCl3)δ1.31(t,J=7.8Hz,3H),1.77(s,3H),1.81(s,3H),2.71(s,3H),2.71(q,J=7.8Hz,2H),3.24(s,3H),3.55(s,3H),3.78(s,3H),4.64(d,J=6.6Hz,2H),5.50(t,J=8.1Hz,2H),6.85(s,1H),7.09(d,J=8.4Hz,1H),7.33-7.38(m,2H),7.52(d,J=8.1Hz,1H),7.58(s,1H),7.84(brs,1H),7.94(d,J=8.1Hz,1H)IR(KBr)3434,3350,2938,1727,1523,1480,1368,1248,1178,1165,1080,972,816,802,522cm-1 |
I-1006 | mp91-93℃1H NMR(CDCl3)δ1.30(t,J=7.5Hz,3H),1.75(s,6H),1.79(s,3H),1.81(s,3H),2.55(q,J=7.5Hz,2H),3.48(s,3H),3.74(s,3H),3.79(d,J=6.3Hz,2H),4.61(d,J=6.6Hz,2H),5.41(t,J=6.0Hz,1H),5.53(t,J=6.9Hz,1H),5.67(brs,1H),5.94(brs,1H),6.48(s,1H),6.72(d,J=8.4Hz,1H),6.95(s,2H),7.07(s,1H),7.37-7.45(m,2H),7.64(d,J=7.5Hz,1H),IR(KBr)3433,2932,1609,1521,1489,1461,13958,1308,1286,1245,1192,1114,1072,1011,811cm-1 |
I-1007 | mp71-72℃1H NMR(CDCl3)δ1.31(t,J=7.5Hz,3H),1.76(s,3H),1.82(s,3H),2.60(q,J=7.2Hz,2H),3.47(s,3H),3.75(s,3H),4.61(d,J=6.6Hz,2H),5.53(t,J=6.9Hz,2H),5.69(brs,1H),5.93(brs,1H),6.47(s,1H),6.78(d,J=8.1Hz,1H),6.95(s,2H),7.06(s,1H),7.26(s,1H),7.39(s,1H)IR(KBr)3436,2932,1620,1584,1519,1487,1459,1397,1285,1242,1112,1072,819cm-1 |
I-1008 | mp171-173℃1HNMR(CDCl3)δ3.46(s,3H),3.75(s,3H),5.15(s,2H),5.68(s,1H),5.88(s,1H),6.44(s,1H),6.95(dd,J=8.4,1.9Hz,1H),7.03(d,J=8.4Hz,1H),7.08(d,J=1.9Hz,1H),7.37-7.48(m,7H),7.59(d,J=8.4Hz,2H)IR(KBr)3544,3514,3462,1517,1482,1388,1284,1247,1089,1107,1069,1006,938,822cm-1 |
I-1009 | mp180-182℃1H NMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.53(s,3H),3.77(s,3H),5.19(s,2H),6.83(s,1H),7.15(d,J=8.4Hz,1H),7.32-7.49(m,9H),7.57(d,J=8.7Hz,2H)IR(KBr)1518,1478,1370,1177,1085,1012,813,797cm-1 |
I-1010 | mp128-130℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.46(s,3H),3.75(s,3H),4.62(d,J=7.0Hz,2H),5.53(t,J=7.0Hz,1H),5.69(s,1H),5.85(s,1H),6.44(s,1H),6.93(dd,J=8.4,1.6Hz,1H),6.97(d,J=8.4Hz,1H),7.05(d,J=1.6Hz,1H),7.42(d,J=8.4Hz,2H),7.59(d,J=8.4Hz,2H)IR(KBr)1517,1482,1287,1244,1106,1070,1013,822,783cm-1 |
I-1011 | mp138-140℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.72(s,3H),3.23(s,3H),3.54(s,3H),3.78(s,3H),4.64(d,J=6.5Hz,2H),5.49(t,J=6.5Hz,1H),6.83(s,1H),7.09(d,J=8.3Hz,1H),7.34(dd,J=8.3,2.0Hz,1H),7.39(d,J=2.0Hz,1H),7.43(d,J=8.6Hz,2H),7.57(d,J=8.6Hz,2H)IR(KBr)1518,1478,1369,1177,1083,972,814,795cm-1 |
I-1012 | mp135-138℃1H NMR(CDCl3)δ1.55-1.63(m,2H),1.77(s,5H),1.83(s,6H),4.56(d,J=6.6Hz,4H),4.66(d,J=4.5Hz,4H),5.50-5.58(m,2H),6.96-7.01(m,4H),7.32-7.38(m,4H),7.45(s,2H)IR(KBr)3339,2914,1609,1520,1488,1385,1289,1238,1177,1000,834,651cm-1 |
I-1013 | mp202-205℃1H NMR(CDCl3+CD3OD)δ1.78(s,3H),1.82(s,3H),4.57(d,J=6.6Hz,2H),4.62(s,4H),5.50-5.56(m,1H),6.86-7.00(m,4H),7.24-7.37(m,4H),7.44(s,2H)IR(KBr)3399,2974,2930,1610,1522,1489,1438,1383,1238,1176,999,903,838,538cm-1 |
I-1014 | mp219-221℃1H NMR(CDCl3)δ2.22(s,3H),2.69(s,3H),3.13(s,3H),3.53(s,3H),3.77(s,3H),5.19(s,2H),6.85(s,1H),7.15(d,J=8.4Hz,1H),7.32-7.49(m,7H),7.60(s,4H)IR(KBr)3384,1701,1604,1524,1482,1355,1294,1176,1084,1011,945,818cm-1 |
I-1015 | mp173-175℃1H NMR(DMSO-d6)δ1.74(s,3H),1.77(s,3H),2.08(s,3H),2.87(s,3H),3.35(s,3H),3.47(s,3H),3.77(s,3H),4.68(d,J=6.4Hz,2H),5.48(t,J=6.4Hz,1H),7.02(s,1H),7.26-7.29(m,3H),7.57(d,J=8.7Hz,2H),7.70(d,J=8.7Hz,2H),10.07(s,1H)IR(KBr)3383,1704,1235,1524,1481,1360,1177,1083,976,816cm-1 |
I-1016 | mp144-145℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.70(s,3H),3.21(s,3H),3.52(s,3H),3.69(d,J=1.6Hz,3H),4.65(d,J=6.8Hz,2H),5.53(t,J=6.8Hz,1H),7.08(t,J=8.4Hz,1H),7.16(dd,J=8.4,1.8Hz,1H),7.20(dd,J=11.7,1.8Hz,1H),7.41(d,J=8.8Hz,2H),7.59(dd,J=8.8,1.4Hz,2H)IR(KBr)1521,1470,1368,1265,1177,1151,1038,971,875cm-1 |
I-1017 | mp196-198℃1H NMR(1MSO-d6)δ1.72(s,3H),1.76(s,3H),2.07(s,3H),3.31(s,3H),3.65(s,3H),4.55(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),6.43(s,1H),6.65(dd,J=8.4,1.9Hz,1H),6.73(d,J=1.9Hz,1H),6.90(d,J=8.4Hz,1H),7.55(d,J=8.6Hz,2H),7.66(d,J=8.6Hz,2H),8.58(brs,1H),8.70(brs,1H),10.02(s,1H)IR(KBr)3358,1661,1596,1523,1489,1396,1308,1254,1227,1114,1074cm-1 |
I-1018 | mp141-143℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.40(s,3H),3.64(d,J=0.9Hz,3H),4.64(d,J=6.9Hz,2H),4.89(s,1H),5.56(t,J=6.9Hz,1H),5.70(s,1H),6.94(d,J=8.7Hz,2H),7.06(t,J=8.7Hz,1H),7.21(ddd,J=8.4,2.1,1.1Hz,1H),7.27(dd,J=12.3,2.1Hz,1H),7.44(dd,J=8.7,1.5Hz,2H)IR(KBr)3485,1523,1466,1402,1266,1173,1036,961,918,837,814cm-1 |
I-1019 | mp81-82℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.26(s,3H),2.72(s,3H),3.23(s,3H),3.57(s,3H),3.79(s,3H),4.64(d,J=6.3Hz,2H),5.49(t,J=6.3Hz,1H),6.83(s,1H),7.09(d,J=8.4Hz,1H),7.33-7.39(m,2H),7.48(s,1H),7.82(d,J=6.0Hz,1H),7.88(s,1H),8.32(brs,1H)IR(KBr)3382,2939,1736,1520,1483,1365,1293,1178,1119,1078,958,802,521cm-1 |
I-1020 | mp93-94℃1H NMR(CDCl3)δ2.62(s,3H),2.99(s,3H),3.15(s,3H),3.20(s,3H),3.83(s,3H),5.21(s,2H),6.91(s,2H),7.17(d,J=8.2Hz,1H),7.35-7.48(m,8H),7.63(d,J=8.4Hz,2H)IR(KBr) 3434,3033,2938,1611,1520,1479,1366,1179,1151,1085,969,850,793,519cm-1 |
I-1021 | mp74-75℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.48(s,3H),3.75(s,3H),4.61(d,J=6.3Hz,2H),5.53(t,J=5.4Hz,1H),5.69(brs,1H),5.86(brs,1H),6.42(s,1H),6.83(d,J=8.7Hz,1H),6.91-6.98(m,2H),7.04(s,1H),7.62(d,J=8.7Hz,1H),7.73(s,1H)IR(KBr)3495,3398,2935,1633,1522,1487,1291,1246,1112,1072,821,788cm-1 |
I-1022 | mp76-77℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),1.84(s,3H),3.52(s,3H),3.78(s,3H),4.63(d,J=6.9Hz,2H),5.53(t,J=6.6Hz,1H),5.74(brs,1H),5.80(brs,1H),6.47(s,1H),6.92-7.00(m,2H),7.04(s,1H),7.38(d,J=8.1Hz,1H),7.93(d,J=8.1Hz,1H),8.04(s,1H)IR(KBr)3411,2934,1662,1519,1488,1425,1309,1245,1175,1128,1071,1050cm-1 |
I-1023 | mp81-82℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.66(s,3H),2.99(s,3H),3.18(s,3H),3.25(s,3H),3.82(s,3H),4.64(d,J=6.6Hz,2H),5.49(t,J=6.0Hz,1H),6.90(s,1H),7.10(d,J=8.4Hz,1H),7.38-7.43(m,3H),7.62(d,J=8.8Hz,1H),8.02(s,1H)IR(KBr)3434,3027,2938,1672,1611,1520,1479,1365,1179,1117,1074,970,847,793,519cm-1 |
I-1024 | mp77-79℃1H NMR(CDCl3)δ1.78(s,3H),1.83(s,3H),3.77(s,3H),4.63(d,J=6.6Hz,2H),5.53(t,J=6.2Hz,1H),5.76(brs,2H),6.52(s,1H),6.91-7.02(m,6H),7.46(d,J=8.4Hz,2H)IR(KBr)3465,2935,1613,1586,1524,1487,1359,1282,1245,1222,1173,1157,1112,1065,974,857,521cm-1 |
I-1025 | mp78-79℃1H NMR(CDCl3)δ2.73(s,3H),2.78(s,3H),3.15(s,3H),3.21(s,3H),3.62(s,3H),5.22(s,2H),7.20(d,J=8.4Hz,1H),7.37-7.44(m,10H),7.68(d,J=8.8Hz,2H)IR(KBr)3433,3032,2939,1519,1473,1366,1178,1151,1004,966,870,847,795,524cm-1 |
I-1026 | mp158-159℃1H NMR(CDCl3)δ1.47(t,J=6.9Hz,3H),2.41(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),4.14(q,J=6.9Hz,2H),5.22(s,2H),6.83(s,1H),6.91(dd,J=2.1,8.1Hz,1H),6.96-7.01(m,2H),7.28-7.48(m,7H),7.66-7.72(m,2H)IR(KBr)1517,1482,1392,1362,1240,1194,1175,1146,1084,963,878,797cm-1 |
I-1027 | mp106-107℃1H NMR(CDCl3)δ2.27(s,6H),3.87(s,3H),5.20(s,2H),6.93-7.00(m,2H),7.01-7.17(m,5H),7.23-7.52(m,7H)IR(KBr)1607,1522,1490,1467,1455,1383,1294,1267,1246,1178,1125,1028,1011,836,813,744cm-1 |
I-1028 | mp162-163℃1H NMR(CDCl3)δ1.45(t,J=6.9Hz,3H),3.46(s,3H),3.74(s,3H),4.15(q,J=6.9Hz,2H),4.98(s,1H),5.19(s,2H),5.91(s,1H),6.45(s,1H),6.88-6.94(m,2H),6.95-7.03(m,2H),7.05(d,J=1.2Hz,1H),7.27-7.41(m,3H),7.45-7.56(m,4H)IR(KBr)3424,3343,1611,1521,1488,1462,1454,1400,1379,1358,1317,1290,1278,1262,1240,1225,1201,1185,1127,1110,1068,1026,1007,828,731cm-1 |
I-1029 | mp73-74℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.27(s,6H),3.86(s,3H),4.63(d,J=7.2Hz,2H),5.56(m,1H),6.92-7.00(m,2H),7.00-7.16(m,5H),7.26-7.34(m,2H)IR(KBr)1610,1521,1489,1461,1438,1297,1276,1249,1231,1181,1122,1028,985,835cm-1 |
I-1030 | mp86-87℃1H NMR(CDCl3)δ1.46(t,J=6.9Hz,3H),1.75(s,3H),1.79(d,J=0.9Hz,3H),2.54(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),4.12(q,J=6.9Hz,2H),4.63(d,J=6.3Hz,2H),5.53(m,1H),6.84(s,1H),6.93-7.01(m,3H),7.35-7.41(m,2H),7.67-7.73(m,2H)IR(KBr) 1518,1480,1449,1413,1389,1366,1239,1199,1180,1150,1082,970,872,798cm-1 |
I-1031 | mp145-146℃1H NMR(CDCl3)δ1.44(t,J=6.9Hz,3H),1.74(s,3H),1.77(d,J=0.9Hz,3H),3.47(s,3H),3.75(s,3H),4.13(q,J=6.9Hz,2H),4.63(d,J=6.6Hz,2H),5.10(s,1H),5.56(m,1H),5.91(s,1H),6.46(s,1H),6.89-6.94(m,2H),6.95-7.03(m,3H),7.50-7.56(m,2H)IR(KBr)3404,1611,1520,1487,1464,1442,1391,1358,1293,1264,1237,1224,1192,1112,1071,1030,1002,831cm-1 |
I-1032 | mp142-145℃1H NMR(CDCl3)δ3.13(s,3H),3.21(s,3H),4.63(s,2H),4.65(s,2H),5.19(s,2H),7.15(d,J=8.4Hz,1H),7.33-7.52(m,13H)IR(KBr)3519,3422,3380,3032,2933,1611,1519,1487,1364,1171,1148,1109,969,871,817,527cm-1 |
I-1033 | mp103-106℃1H NMR(CDCl3+CD3OD)δ1.78(s,3H),1.82(s,3H),3.22(s,3H),3.24(s,3H),4.58-4.67(m,6H),5.46-5.54(m,1H),7.09(d,J=8.4Hz,1H),7.33-7.53(m,8H)IR(KBr)3512,3414,3012,2941,1612,1519,1488,1362,1335,1146,997,972,876,524cm-1 |
I-1034 | mp184-187℃1H NMR(CDCl3+CD3OD)δ1.78(s,3H),1.82(s,3H),4.59-4.65(m,6H),5.52-5.59(m,1H),6.84-6.98(m,5H),7.23-7.28(m,2H),7.44(s,1H),7.45(s,1H)IR(KBr)3400,2931,1611,1521,1491,1247,1203,1009,987,834cm-1 |
I-1035 | mp95-96℃1H NMR(CDCl3)δ2.27(s,6H),2.41(s,3H),5.19(s,2H),7.02-7.18(m,5H),7.22-7.54(m,9H)IR(KBr)1522,1512,1454,1377,1309,1297,1274,1267,1236,1125,1008,877,822,742,696cm-1 |
I-1036 | mp95-96℃1H NMR(CDCl3)δ2.24(s,3H),2.27(s,3H),5.19(s,2H),6.99-7.15(m,5H),7.26-7.52(m,9H)IR(KBr)1518,1499,1482,1454,1380,1300,1278,1262,1227,1125,1090,1021,1015,875,834,817,739cm-1 |
I-1037 | mp58-59℃1H NMR(CDCl3)δ1.77(d,J=0.6Hz,3H),1.81(d,J=0.9Hz,3H),2.27(s,6H),2.41(s,3H),4.63(d,J=6.6Hz,2H),5.56(m,1H),6.98-7.14(m,5H),7.21-7.29(m,4H)IR(KBr)1520,1490,1460,1444,1385,1294,1271,1262,1232,1125,1001,828,818cm-1 |
I-1038 | mp67-68℃1H NMR(CDCl3)δ1.77(s,3H),1.81(d,J=0.9Hz,3H),2.25(s,3H),2.27(s,3H),4.64(d,J=6.6Hz,2H),5.55(m,1H),6.90-7.14(m,5H),7.26-7.32(m,2H),7.36-7.42(m,2H)IR(KBr)1518,1500,1482,1466,1309,1299,1267,1229,1124,1090,995,834cm-1 |
I-1039 | mp153-155℃1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.84(d,J=4.2Hz,2H),6.43~6.51(m,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.94~7.00(m,2H),7.08(brs,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3411,1612,1588,1523,1489,1288,1245,1224,1113,1070,1011,938,824cm-1 |
I-1040 | 泡沫1H NMR(CDCl3)δ3.28(d,J=2.4Hz,1H),3.45(s,3H),3.75(s,3H),4.94(dd,J=6.0,1.8Hz,2H),5.74(ddt,J=11.1,2.4,1.8Hz,1H),6.27(dt,J=11.1,6.0Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.94~7.00(m,2H),7.07(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3433,3279,1612,1588,1523,1489,1286,1248,1223,1113,1070,1011,938,825cm-1 |
I-1041 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.90(d,J=1.8Hz,2H),5.55(dd,J=10.8,2.4Hz,1H),5.71(dd,J=17.7,2.4Hz,1H),5.85(ddt,J=17.7,10.8,1.8Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.97(dd,J=8.4,2.1Hz,1H),7.07(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3433,1612,1589,1523,1489,1286,1224,1192,1112,1070,1002,937,825,815cm-1 |
I-1042 | mp185-187℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.76(s,3H),3.23(s,3H),3.50(s,3H),3.78(s,3H),4.64(d,J=6.6Hz,2H),5.50(t,J=6.6Hz,1H),6.63(t,J=2.4Hz,1H),6.95(s,1H),7.09(d,J=8.5Hz,1H),7.26-7.29(m,1H),7.37(dd,J=8.5,2.1Hz,1H),7.42(d,J=2.1Hz,1H),7.45-7.51(m,2H),7.89(s,1H),8.26(brs,1H)IR(KBr)3418,1473,1362,1177,1079,961,817,796cm-1 |
I-1043 | mp152-154℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.43(s,3H),3.76(s,3H),4.61(d,J=6.9Hz,2H),5.53(t,J=6.9Hz,1H),5.69(s,1H),5.98(s,1H),6.55(s,1H),6.63(t,J=2.1Hz,1H),6.94-7.01(m,2H),7.10(d,J=0.9Hz,1H),7.25-7.27(m,1H),7.46(d,J=8.4Hz,1H),7.51(dd,J=8.5,1.5Hz,1H),7.89(s,1H),8.24(brs,1H)IR(CHCl3)3529,3480,1515,1495,1407,1291,1246,1107,1070cm-1 |
I-1044 | mp127-128℃1H NMR(CDCl3)δ2.45(s,3H),3.52(s,3H),3.77(s,3H),3.91(s,3H),5.22(s,2H),6.84(s,1H),6.91(dd,J=8.4,2.1Hz,1H),6.79-7.00(m,2H),7.12-7.18(m,2H),7.30-7.47(m,5H),7.59-7.63(m,2H)IR(CHCl3)2938,2843,1606,1585,1520,1483,1464,1443,1390,1368,1174,1141,1083,1013,962,936,865,838cm-1 |
I-1045 | mp124-127℃1H NMR(CDCl3)δ2.46(s,3H),3.55(s,3H),3.77(s,3H),3.91(s,3H),5.21(s,2H),5.42(br,1H),6.82(s,1H),6.90(dd,J=8.4,1.8Hz,1H),6.97-7.10(m,3H),7.29-7.47(m,7H)IR(CHCl3)3579,2938,1600,1523,1484,1464,1393,1368,1327,1282,1174,1141,1081,1036,1012,962,908cm-1 |
I-1046 | mp178-180℃1H NMR(CDCl3)δ2.44(s,3H),3.29(s,3H),3.58(s,3H),3.78(s,3H),3.91(s,3H),5.22(s,2H),6.83(s,1H),8.99(dd,J=8.1,2.1Hz,1H),6.97-7.25(m,2H),7.31-7.58(m,8H)IR(CHCl3)2939,2840,1591,1519,1483,1464,1374,1331,1173,1141,1116,1082,1012,964,863cm-1 |
I-1047 | mp98-99℃1H NMR(CDCl3)δ2.35(s,3H),5.22(s,2H),6.59(t,J F-H=54.6Hz,2H),7.09-7.50(m,12H),7.74-7.75(d,J=4.5Hz,2H)IR(CHCl3)1752,1523,1493,1384,1273,1169,1133,1070,1037,916,851cm-1 |
I-1048 | mp112-114℃1H NMR(CDCl3)δ1.75-1.76(d,J=0.6Hz,3H),1.78-1.79(d,J=0.9Hz,3H),2.57(s,3H),3.53(s,3H),3.78(s,3H),3.89(s,3H),4.62-4.64(d,J=7.5Hz,2H),5.54(s,1H),6.84(s,1H),6.96-6.97(m,3H),7.12-7.18(m,2H),7.59-7.64(m,2H)IR(CHCl3)2938,1606,1583,1519,1483,1464,1443,1416,1389,1368,1175,1141,1083,1038,1013,962,936,865,838cm-1 |
I-1049 | mp203-204℃1H NMR(CD3OD)δ4.53(s,2H),4.55(s,2H),5.21(s,2H),6.84-6.88(m,2H),7.12-7.50(m,12H)IR(KBr)3380,1611,1586,1523,1490,1462,1434,1380,1317,1300,1258,1194,1173,1128,1033,1007,906,871,836,817,787,730,693,646cm-1 |
I-1050 | mp99-100℃1H NMR(CDCl3)δ1.75(s,3H),1.78-1.79(d,J=0.9Hz,3H),3.46(s,3H),3.75(s,3H),3.88(s,3H),4.62-4.64(d,J=6.6Hz,2H),5.57(m,1H),5.89(s,1H),6.46(s,1H),6.96-7.02(m,3H),7.12-7.18(m,2H),7.59-7.64(m,2H)IR(CHCl3)3513,2938,1605,1583,1490,1423,1407,1392,1362,1318,1269,1177,1158,1140,1118,1078,1038,1012,930,846,826cm-1 |
I-1051 | mp153-154℃1H NMR(CDCl3)δ1.76(s,3H),1.79-1.80(d,J=0.9Hz,3H),2.57(s,3H),3.29(s,3H),3.60(s,3H),3.79(s,3H),3.89(s,3H),4.62-4.64(d,J=6.6Hz,2H),5.54(m,1H),6.84(s,1H),6.96-6.97(m,4H),7.46-7.59(m,3H)IR(CHCl3)2938,1592,1519,1483,1464,1374,1332,1239,1173,1141,1116,1082,1038,1011,965,864cm-1 |
I-1052 | 无定形1H NMR(CDCl3)δ2.12(s,3H),3.47(s,3H),5.15(s,2H),5.82-608(m,3H),6.70-6.95(m,5H),7.02(d,J=8.1Hz,1H),7.39-7.52(m,7H)IR(CHCl3)3597,3535,2937,1731,1612,1589,1522,1489,1455,1401,1382,1328,1309,1288,1173,1128,1096,1011,939,835cm-1 |
I-1053 | mp141-142℃1H NMR(CDCl3)δ1.75(s,3H),1.78-1.79(d,J=0.9Hz,3H),3.49(s,3H),3.75(s,3H),3.89(s,3H),4.62-4.64(d,J=6.6Hz,2H),5.30(d,J F-H=3.3Hz,1H),5.57(m,1H),5.88(s,1H),6.45(s,1H),6.99-7.11(m,4H),7.33(m,1H),7.43(dd,J=11.7,2.1Hz,1H)IR(CHCl3)3578,3514,1621,1600,1583,1523,1492,1464,1397,1320,1279,1175,1140,1116,1100,1076,1038,1011,902cm-1 |
I-1054 | mp138-140℃1H NMR(CDCl3)δ5.17(s,2H),5.60(s,1H),5.72(s,1H),6.98-7.02(m,2H),7.10-7.14(m,3H),7.18(s,1H),7.35(s,1H),7.37-7.47(m,5H),7.59-7.61(m,2H)IR(KBr)3600-2800(br),1590,1528,1503,1483,1454,1386,1294,1254,1223,1187,1132,1086,1009cm-1 |
I-1055 | mp176-178℃1H NMR(CDCl3)δ3.13(s,3H),3.32(s,3H),5.19(s,2H),7.16(d,J=8.7Hz,1H),7.37-7.55(m,9H),7.61-7.64(m,4H)IR(KBr)3600-2800(br),1611,1525,1503,1469,1359,1290,1244,1170,1088,979cm-1 |
I-1056 | mp134-136℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),3.23(s,3H),3.32(s,3H),4.64(d,J=6.9Hz,1H),5.48-5.54(m,1H),7.10(d,J=8.4Hz,1H),744-7.55(m,4H),7.58-7.65(m,4H)IR(KBr)3600-2800(br),1609,1527,1504,1469,1351,1289,1277,1186,1171,1115,1089,973cm-1 |
I-1057 | mp97-100℃1H NMR(CDCl3)δ1.77(d,J=0.9Hz,3H),1.82(d,J=0.9Hz,3H),4.63(d,J=7.2Hz,2H),5.50-5.54(m,1H),5.62(brs,1H),5.74(brs,1H),6.95(d,J=8.7Hz,1H),7.12(dd,J=2.4,8.7Hz,1H),7.18(s,1H),7.24(d,J=2.4Hz,1H),7.36(s,1H),7.42-7.46(m,2H),7.58-7.62(m,2H)IR(KBr)3600-2800(br),1599,1588,1528,1482,1385,1326,1289,1252,1212,1193,1132,1112,1084,1056,1001cm-1 |
I-1058 | mp216-218℃1H NMR(DMSO-d6)δ2.93(s,12H),3.73(s,6H),6.74-6.79(m,4H),6.92(s,2H),7.38-7.43(m,4H)IR(KBr)3600-2800(br),1616,1533,1496,1458,1442,1387,1360,1230,1202,1169,1059,1035cm-1 |
I-1059 | mp122-123℃1H NMR(CDCl3)δ1.74(d,J=0.6Hz,3H),1.78(d,J=0.6Hz,3H),2.26(s,3H),2.29(s,3H),3.77(d,J=6.9Hz,2H),4.83(br,1H),5.36-5.41(m,1H),6.61-6.77(m,1H),6.86.6.91(m,2H),6.99-7.04(m,2H),7.10(s,1H),7.11(s1H),7.21-7.26(m,2H)IR(KBr)3600-2800(br),1626,1608,1526,1489,1428,1336,1300,1252,1209,1187cm-1 |
I-1060 | mp泡沫1H NMR(CDCl3)δ1.74(s,3H),1.77(s,3H),2.27(s,3H),2.31(s,3H),3.76(d,J=6.6Hz,2H),3.86(s,3H),5.38-5.43(m,1H),6.66(d,J=8.1Hz,1H),6.80(d,J=1.8Hz,1H),6.86-6.90(m,3H),7.11(s,1H),7.16(s,1H),7.23-7.26(m,2H)IR(CHCl3)3600-2800(br),1730,1611,1525,1489,1455,1256,1171,1137,1100,1036cm-1 |
I-1061 | mp191-193℃1H NMR(CDCl3)δ3.01(s,6H),3.79(s,3H),3.80(s,3H),6.79-6.83(m,2H),6.92(s,1H),6.98(s,1H),7.41-7.51(m,4H),8.12(brs,1H),8.26-8.32(m,1H)IR(KBr)3600-2800(br),1712,1617,1600,1536,1494,1460,1446,1385,1364,1290,1212,1162,1057,1035cm-1 |
I-1062 | mp240-245℃1H NMR(CDCl3)δ3.82(s,6H),6.95(s,2H),7.41-7.49(m,4H),8.13(brs,2H),8.29-8.35(m,1H)IR(KBr)3600-2800(br),1725,1598,1544,1492,1381,1294,1215,1197,1165,1109,1055,1033cm-1 |
I-1063 | 1H NMR(CDCl3)δ1.99(s,6H),2.17(s,3H),3.21(s,3H),5.20(s,2H),6.95-7.11(m,4H),7.23(d,J=8.7Hz,2H),7.33-7.52(m,7H)IR(KBr) 1617,1577,1513,1366,1295,1267,1198,1173,1149,1127,1106cm-1 |
I-1064 | 1H NMR(CDCl3)δ1.99(s,6H),2.17(s,3H),3.21(s,3H),5.18(d,J=3.9Hz,1H),6.97-7.10(m,4H),7.23(d,J=8.7Hz,2H),7.37(d,J=8.7Hz,2H)IR(KBr)3442,1620,1597,1519,1472,1356,1279,1232,1174,1147,1103cm-1 |
I-1065 | 1H NMR(CDCl3)δ1.78(s,3H),1.83(s,3H),2.00(s,6H),2.19(s,3H),3.22(s,3H),4.65(d,J=6.3Hz,2H),5,52-5.62(m,1H),6.96-7.13(m,4H),7.24(d,J=8.7Hz,2H),7.38(d,J=8.7Hz,2H)IR(KBr)1617,1576,1514,1466,1359,1297,1268,1204,1151,1002cm-1 |
I-1066 | 1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.01(s,6H),2.18(s,3H),4.63(d,J=6.9Hz,2H),4.75(s,1H),5.52-5.60(m,1H),6.82-7.11(m,8H)IR(KBr)3433,1606,1517,1466,1297,1269,1221,1128,1107,1004cm-1 |
I-1067 | 1HNMR(CDCl3)δ:2.25(s,3H),2.27(s,3H),2.31(s,3H),3.20(s,3H),4.75(s,1H),6.83(d,J=8.4Hz,1H),7.05-7.14(m,4H),7.34(d,J=8.4Hz,2H),7.42(d,J=8.4Hz,2H)IR(KBr)3494,3435,1604,1517,1488,1375,1327,1199,1171,1148,1118cm-1 |
I-1068 | 1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.25(s,3H),2.28(s,6H),3.20(s,3H),4.58(d,J=6.6Hz,2H),5.50-5.58(m,1H),6.88(d,J=9.0Hz,1H),7.08-7.16(m,4H),7.34(d,J=8.7Hz,2H),742(d,J=8.7Hz,2H)IR(KBr)1604,1513,1486,1367,1238,1176,1153,1131,1002cm-1 |
I-1069 | 1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.26(s,3H),2.28(s,6H),4.57(d,J=6.6Hz,2H),4.80(s,1H),5.50-5.58(m,1H),6.85-6.91(m,3H),7.09-7.17(m,3H),7.21-7.28(m,3H)IR(KBr)3436,1608,1518,1488,1238,1130,1008cm-1 |
I-1070 | 1H NMR(CDCl3)δ:2.26(s,3H),2.30(s,3H),3.00(s,6H),5.19(s,2H),6.80(d,J=8.7Hz,2H),7.02-7.16(m,5H),7.26(d,J=8.7Hz,2H),7.33-7.51(m,5H)IR(KBr)1608,1527,1490,1355,1297,1270,1262,1231,1121,1022cm-1 |
I-1071 | 1H NMR(CDCl3)δ2.26(s,3H),2.30(s,3H),3.01(s,6H),5.09(s,1H),6.80(d,J=8.4Hz,2H),7.01-7.15(m,5H),7.27(d,J=8.4Hz,2H)IR(KBr)3432,1613,1590,1526,1489,1307,1283,1241,1138,1111cm-1 |
I-1072 | 1H NMR(CDCl3)δ:1.77(s,3H),1.81(s,3H),2.27(s,3H),2.30(s,3H),3.00(s,6H),4.63(d,J=6.6Hz,2H),5.51-5.59(m,1H),6.80(d,J=8.4Hz,2H),6.97-7.16(m,5H),7.27(d,J=8.14Hz,2H)IR(KBr)1611,1528,1489,1353,1297,1266,1228,1122,1011cm-1 |
I-1073 | mp182-184℃1H NMR(CDCl3)δ1.48(s,3H),1.67(s,3H),1.91(s,3H),3.46(s,3H),3.76(s,3H),3.84(s,3H),3.94-4.03(m,1H),4.05-4.59(m,1H),5.23-5.32(m,1H),5.74(brs,1H),6.05(s,1H),6.48(s,1H),6.93-6.99(m,2H),7.04-7.10(m,3H),7.51-7.56(m,3H)IR(KBr)3400,2934,1625,1523,1396,1227,1119,1077,1036,826,589cm-1 |
I-1074 | mp153-154℃1H NMR(CDCl3)δ1.74(s,3H),1.78(s,3H),2.30(s,3H),2.31(s,3H),3.75(d,J=6.6Hz,2H),3.86(s,3H),3.87(s,3H),5.37-5.45(m,1H),6.66(d,J=8.4Hz,1H),6.74-6.83(m,5H),6.89(dd,J=1.8,8.1Hz,1H),7.14(s,1H),7.16(s,1H)IR(KBr)3408,3389,3294,3210,2919,2835,1528,1495,1275,1208,1032,856,826cm-1 |
I-1075 | mp168-171℃1H NMR(CDCl3)δ1.74(s,6H),1.77(s,6H),2.31(s,6H),3.75(d,J=6.9Hz,4H),3.86(s,6H),5.37-5.45(m,2H),6.66(d,J=8.1Hz,2H),6.80(d,J=1.8Hz,2H),6.89(dd,J=1.8,8.1Hz,2H),7.16(s,1H)IR(KBr)3423,2968,2927,2912,2849,1609,1526,1498,1454,1261,1209,1135,1030,855,803cm-1 |
I-1076 | mp79-80℃1H NMR(CDCl3)δ2.54(s,3H),3.19(s,3H),3.85(s,3H),5.17(s,2H),5.71(brs,1H),6.93(d,J=8.1Hz,1H),7.01-7.07(m,3H),7.24-7.26(m,2H),7.37-7.43(m,7H),7.66(d,J=8.7Hz,2H)IR(KBr)3466,3029,2939,2937,1610,1520,1482,1365,1246,1201,1175,1150,1073,969,872,839,804cm-1 |
I-1077 | mp151-152℃1HNMR(CDCl3)δ4.00(s,3H),4.91(brs,1H),5.24(s,2H),6.89(d,J=8.2Hz,2H),7.00(d,J=8.0Hz,1H),7.12-7.47(m,10H),7.71(d,J=7.4Hz,1H),7.89(s,1H)IR(KBr)3422,1612,1526,1491,1454,1329,1287,1269,1248,1171,1136,1103,1019,827cm-1 |
I-1078 | mp173-174℃1H NMR(CDCl3)δ3.13(s,3H),4.92(brs,1H),5.19(s,2H),6.88(d,J=8.6Hz,2H),7.15-7.26(m,4H),7.35-7.59(m,7H),7.69(d,J=9.4Hz,1H),7.86(s,1H)IR(KBr)3426,1613,1527,1489,1435,1361,1330,1294,1243,1164,1118,1070,978,821cm-1 |
I-1079 | mp168-169℃1H NMR(CDCl3)δ3.20(s,3H),3.99(s,3H),5.22(s,2H),6.89(d,J=8.8Hz,1H),7.11-7.15(m,2H),7.31-7.49(m,10H),7.73(d,J=7.4Hz,1H),7.90(s,1H)IR(KBr)3434,1603,1524,1488,1369,1335,1244,1178,1143,1119,1006,871cm-1 |
I-1080 | mp68-69℃1H NMR(CDCl3)δ3.13(s,3H),3.19(s,3H),5.19(s,2H),7.18(d,J=8.6Hz,2H),7.26-7.59(m,11H),7.73(d,J=9.2Hz,1H),7.89(s,1H)IR(KBr)3431,3034,2938,1613,1524,1487,1367,1330,1293,1242,1175,1151,1118,970,872,828cm-1 |
I-1081 | mp74-76℃1H NMR(CDCl3)δ1.78(s,3H),1.84(s,3H),3.51(s,3H),4.64(d,J=5.6Hz,2H),5.08(brs,2H),5.49-5.54(m,1H),5.75(brs,1H),5.8(brs,1H),6.14(s,1H),6.89-7.12(m,5H),7.53(d,J=8.4Hz,2H)IR(KBr)3444,2934,1612,1523,1485,1403,1360,1251,1172,1006,971,837,527cm-1 |
I-1082 | mp71-72℃1H NMR(CDCl3)δ2.46(s,3H),3.20(s,3H),3.86(s,3H),3.91(s,3H),5.21(s,2H),6.87-7.03(m,3H),7.11(s,1H),7.24-7.41(m,8H),7.67(d,J=8.8Hz,2H)IR(KBr)3434,3028,2936,1609,1521,1482,1365,1239,1176,1074,969,869,804cm-1 |
I-1083 | mp73-74℃1H NMR(CDCl3)δ2.66(s,3H),3.13(s,3H),3.20(s,3H),3.86(s,3H),5.19(s,2H),7.08(d,J=1.6Hz,1H),7.16(d,J=8.4Hz,1H),7.21-7.28(m,2H),7.37-7.42(m,8H),7.66(d,J=8.4Hz,2H)IR(KBr)3432,3031,2938,1610,1523,1480,1365,1176,1151,1074,970,875,807,524cm-1 |
I-1084 | mp110-111℃1H NMR(CDCl3)δ1.78(s,3H),1.81(s,3H),3.21(s,3H),3.98(s,3H),4.67(d,J=6.6Hz,2H),5.57(t,J=6.8Hz,1H),7.01(d,J=8.0Hz,1H),7.15-7.21(m,2H),7.28-7.45(m,4H),7.76(d,J=7.6Hz,H),7.93(s,1H),8.03(s,1H)IR(KBr)3434,3010,2931,1524,1488,1368,1336,1247,1173,1149,1121,1007,871,562cm-1 |
I-1085 | mp147-148℃1H NMR(CDCl3)δ1.76(s,3H),1.79(s,3H),3.96(s,3H),4.65(d,J=6.3Hz,2H),4.91(brs,1H),5.55(t,J=5.7Hz,1H),6.88(d,J=8.1Hz,2H),6.99(d,J=8.4Hz,1H),7.12-7.26(m,4H),7.36(d,J=8.1Hz,1H),7.89(s,1H)IR(KBr)3450,2938,1612,1524,1490,1436,1340,1264,1230,1212,1139,1123,984,835cm-1 |
I-1086 | mp134-135℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),4.64(d,J=6.6Hz,2H),4.84(brs,1H),5.52(t,J=7.2Hz,1H),5.77(s,1H),6.87(d,J=8.7Hz,2H),6.96(d,J=8.4Hz,1H),7.12(dd,J=2.4,8.7Hz,1H),7.35(d,J=8.1Hz,1H),7.70(d,J=8.4Hz,1H),7.89(s,1H)IR(KBr)3367,1610,1489,1442,1333,1265,1193,1165,1124,834,805cm-1 |
I-1087 | mp156-157℃1HNMR(CDCl3)δ1.78(s,3H),1.81(s,3H),3.82(s,3H),3.89(s,3H),4.65(d,J=6.2Hz,2H),4.95(brs,1H),5.22(brs,1H),5.58(t,J=6.0Hz,1H),6.73(s,1H),6.87-7.00(m,6H),7.53(d,J=8.4Hz,2H)IR(KBr) 3394,2934,1610,1526,1499,1455,1402,1240,1221,1139,1099,894,815cm-1 |
I-1088 | mp69-70℃1H NMR(CDCl3)δ1.77(s,3H),1.83(s,3H),3.80(s,3H),4.63(d,J=7.0Hz,2H),4.93(brs,1H),5.22(brs,1H),5.52(t,J=7.0Hz,1H),5.78(brs,1H),6.70(d,J=1.6Hz,1H),6.83-7.01(m,6H),7.51(d,J=8.8Hz,2H)IR(KBr) 3411,2933,1611,1526,1492,1453,1263,1242,1220,1190,1172,1096,907,822cm-1 |
I-1089 | mp160-161℃1HNMR(CDCl3)δ1.39(d,J=6.0Hz,6H),2.40(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),4.55(m,1H),5.20(s,2H),6.83(s,1H),6.93(dd,J=1.8,8.1Hz,1H),7.01(d,J=8.1Hz,1H),7.01(d,J=1.8Hz,1H),7.28-7.48(m,7H),7.66-7.72(m,2H)IR(KBr)1515,1480,1463,1391,1363,1239,1192,1176,1149,1082,1018,962,873,800cm-1 |
I-1090 | mp154-155℃1H NMR(CDCl3)δ2.59(s,3H),3.21(s,3H),3.54(s,3H),3.77(s,3H),5.23(s,2H),6.84(s,1H),7.06(d,J=8.4Hz,1H),7.24-7.50(m,9H),7.65-7.71(m,2H)IR(KBr)1513,1479,1365,1267,1232,1178,1150,1079,971,959,875,797cm-1 |
I-1091 | mp137-138℃1H NMR(CDCl3)δ1.38(d,J=6.3Hz,6H),346(s,3H),3.74(s,3H),4.54(m,1H),4.96(s,1H),5.17(s,2H),5.92(s,1H),6.45(s,1H),6.89-6.94(m,2H),7.00-7.11(m,3H),7.27-7.41(m,3H),7.45-7.56(m,4H)IR(KBr)3443,3356,1611,1521,1488,1458,1393,1269,1236,1138,1112,1074,1013,830,743cm-1 |
I-1092 | mp75-76℃1H NMR(CDCl3)δ1.37(d,J=5.8Hz,6H),1.75(s,3H),1.79(s,3H),2.53(s,3H),3.21(s,3H),3.56(s,3H),3.78(s,3H),4.51(m,1H),4.61(d,J=6.6Hz,2H),5.52(m,1H),6.84(s,1H),6.96-7.02(m,3H),7.34-7.42(m,2H),7.65-7.74(m,2H)IR(KBr)1516,1480,1449,1360,1332,1240,1199,1177,1152,1083,964,873,797cm-1 |
I-1093 | mp119-120℃1H NMR(CDCl3)δ1.37(d,J=6.3Hz,6H),1.73(s,3H),1.77(d,J=0.9Hz,3H),3.46(s,3H),3.75(s,3H),4.51(m,1H),4.61(d,J=6.6Hz,2H),5.14(s,1H),5.54(m,1H),5.93(s,1H),6.46(s,1H),6.89-6.95(m,2H),6.98(d,J=8.1Hz,1H),7.01-7.07(m,2H),7.50-7.56(m,2H)IR(KBr)3426,1610,1522,1488,1455,1402,1267,1237,1174,1135,1112,1079,1020cm-1 |
I-1094 | mp150-151℃1H NMR(CDCl3)δ3.44(s,3H),3.75(s,3H),4.90(s,1H),5.20(s,2H),5.99(s,1H),6.44(s,1H),6.88-6.95(m,2H),7.04(d,J=8.4Hz,1H),7.29-7.44(m,4H),7.47-7.56(1m,5H)IR(KBr)3410,1610,1519,1484,1463,1455,1410,1382,1359,1285,1264,1229,1118,1074,1060,1014,995cm-1 |
I-1095 | 1H NMR(CDCl3)δ0.96(s,3H),0.98(s,3H),1.53-1.82(m,3H),2.99(s,6H),3.20(t,J=7.2Hz,2H),3.78(s,3H),3.79(s,3H),3.87(br,1H),6.71-6.83(m,3H),6.92(s,1H),6.94(s,1H),7.23-7.31(m,2H),7.47-7.52(m,2H) |
I-1096 | mp87-89℃1H NMR(CDCl3)δ1.70(s,3H),1.75(s,3H),2.82(s,3H),3.00(s,3H),3.74-3.80(m,2H),3.78(s,3H),3.80(s,3H),5.29-5.34(m,1H),6.79-6.83(m,2H),6.92-6.97(m,3H),7.25-7.34(m,2H),7.47-7.52(m,2H)IR(KBr)3600-2800(br),1613,1531,1495,1460,1448,1380,1359,1253,1210,1057,1036cm-1 |
I-1097 | mp167-169℃1H NMR(CDCl3)δ2.92(s,3H),3.00(s,6H),3.78(s,3H),3.79(s,3H),4.02(br,1H),6.71-6.83(m,3H),6.92(s,1H),6.95(s,1H),7.25-7.32(m,2H),7.47-7.52(m,2H)IR(KBr)3600-2800(br),1625,1613,1533,1497,1462,1445,1381,1358,1328,1262,1205,1163,1051,1031cm-1 |
I-1098 | mp114-115℃1H NMR(CDCl3)δ2.27(s,6H),2.54(s,3H),5.19(s,2H),7.00-7.16(m,5H),7.26-7.51(m,9H)IR(KBr)1519,1501,1483,1454,1310,1295,1263,1232,1123,998,744cm-1 |
I-1099 | mp68-69℃1H NMR(CDCl3)δ1.62(brs,1H),1.77(s,3H),1.82(s,3H),2.27(s,3H),2.28(s,3H),4.64(d,J=6.8Hz,2H),4.76(s,2H),5.56(m,1H),7.00-7.16(m,5H),7.33-7.48(m,4H)IR(KBr)3433,1522,1490,1384,1311,1296,1266,1232,1194,1122,1025,1013,992,841,818cm-1 |
I-1100 | mp68-69℃1H NMR(CDCl3)δ1.62(brs,1H),1.77(s,3H),1.82(s,3H),2.27(s,3H),2.28(s,3H),4.64(d,J=6.8Hz,2H),4.76(s,2H),5.56(m,1H),7.00-7.16(m,5H),7.33-7.48(m,4H)IR(KBr)3433,1522,1490,1384,1311,1296,1266,1232,1194,1122,1025,1013,992,841,818cm-1 |
I-1101 | mp171℃1H NMR(CDCl3)δ1.77(s,3H),1.81(d,J=0.9Hz,3H),2.68(s,3H),3.21(s,3H),3.55(s,3H),3.78(s,3H),4.65(d,J=6.6Hz,2H),5.53(m,1H),6.84(s,1H),7.03(d,J=8.7Hz,1H),7.29(dd,J=2.1,8.7Hz,1H),7.36-7.41(m,2H),7.46(d,J=2.1Hz,1H),7.66-7.72(m,2H)IR(KBr)1510,1477,1376,1358,1349,1294,1237,1196,1173,1145,1077,1004,958,861,801cm-1 |
I-1102 | mp168-169℃1H NMR(CDCl3)δ1.76(d,J=0.3Hz,3H),1.80(d,J=0.9Hz,3H),3.44(s,3H),3.75(s,3H),4.64(d,J=6.6Hz,2H),4.97(s,1H),5.55(m,1H),6.00(s,1H),6.45(s,1H),6.89-6.95(m,2H),7.01(d,J=8.4Hz,1H),7.33(dd,J=2.1,8.4Hz,1H),7.51(d,J=2.1Hz,1H),7.51-7.56(m,2H)IR(KBr)3396,1613,1521,1485,1467,1440,1408,1384,1357,1286,1264,1229,1116,1076,1056,993,834cm-1 |
I-1103 | mp176-177℃1H NMR(CDCl3)δ1.77(s,3H),1.80(s,3H),2.09(s,3H),2.16(s,3H),3.87(s,3H),4.65(d,J=7.2Hz,2H),4.78(brs,1H),5.06(s,1H),5.40-5.60(m.1H),6.76(s,1H),6.82-6.91(m,4H),7.02(d,J=7.8Hz,1H),7.22-7.27(m,2H)IR(CHCl3)3597,3533,3026,3010,2921,1731,1612,1520,1488,1240,1172cm-1 |
I-1104 | mp185-186℃1H NMR(CDCl3)δ1.78(s,3H),1.82(s,3H),2.06(s,3H),2.15(s,3H),4.66(d,J=6.9Hz,2H),4.71(s,1H),4.89(s,1H),5.53-5.58(m,1H),6.75(s,1H),6.86-6.91(m,2H),6.90-7.00(m,3H),7.21-7.26(m,2H)IR(CHCl3)3691,3598,3546,3068,2922,1674,1613,1520,1488,1298,1262,1165cm-1 |
I-1105 | mp143-144℃1HNMR(CDCl3)δ2.48(s,3H),3.21(s,3H),3.52(s,3H),3.67(d,J=1.2Hz,3H),3.92(s,3H),5.23(s,2H),6.92-7.02(m,3H),7.31-7.48(m,7H),7.60(dd,J=8.7,1.5Hz,2H)IR(KBr) 1519,1470,1370,1256,1173,1152,1029,872cm-1 |
I-1106 | mp128-130℃1H NMR(CDCl3)δ1.76(s,3H),1.80(s,3H),2.59(s,3H),3.21(s,3H),3.53(s,3H),3.67(d,J=0.9Hz,3H),3.90(s,3H),4.64(d,J=6.9Hz,2H),5.55(t,J=6.9Hz,1H),6.97-7.00(m,3H),7.41(d,J=8.8Hz,2H),7.60(dd,J=8.8,1.1Hz,2H)IR(KBr)1519,1361,1258,1175,1148,1041,978,874cm-1 |
I-1107 | mp168-170℃1H NMR(CDCl3)δ1.76(s,3H),1.79(s,3H),3.43(s,3H),3.63(d,J=0.9Hz,3H),3.89(s,3H),4.65(d,J=6.8Hz,2H),5.01(s,1H),5.57(t,J=6.8Hz,1H),5.65(s,1H),6.90-7.06(m,5H),7.43(dd,J=8.7,1.5Hz,2H)IR(KBr)3433,1523,1464,1397,1253,1216,1038,977,838,814cm-1 |
I-1108 | mp127-128℃1H NMR(CDCl3)δ2.25(s,3H),2.27(s,3H),3.20(s,3H),5.22(s,2H),7.02(d,J=8.4Hz,1H),7.10(s,1H),7.11(s,1H),7.18(dd,J=2.1,8.4Hz,1H),7.31-7.54(m,10H)IR(KBr)1513,1484,1369,1284,1243,1175,1150,1061,984,968,868,847,791,718cm-1 |
I-1109 | mp161-162℃1H NMR(CDCl3)δ2.26(s,3H),2.28(s,3H),5.16(s,2H),5.19(s,2H),5.70(brs,1H),6.82(dd,J=2.1,8.4Hz,1H),6.96-7.16(m,7H),7.31-7.51(m,10H)HR(KBr)3449,1521,1492,1470,1455,1394,1294,1279,1247,1232,1199,1185,1129,1013,740,695cm-1 |
I-1110 | mp133-134℃1H NMR(CDCl3)δ2.26(s,6H),4.80 (brs,1H),5.21(s,2H),6.85-6.93(m,2H),7.02(d,J=8.4Hz,1H),7.09(s,1H),7.17(s,1H),7.15-7.52(m,9H)IR(KBr)3350,1601,1519,1485,1453,1387,1289,1255,1169,1060,839,813,731cm-1 |
I-1111 | mp83-84℃1H NMR(CDCl3)δ1.78(d,J=0.3Hz,3H),1.82(d,J=0.9Hz,3H),2.26(s,3H),2.27(s,3H),3.20(s,3H),4.65(d,J=6.6Hz,2H),5.55(m,1H),6.99(d,J=8.4Hz,1H),7.11(s,1H),7.12(s,1H),7.19(dd,J=2.1,8.4Hz,1H),7.38(d,J=2.1Hz,1H),7.32-7.43(m,4H)IR(KBr)1514,1485,1364,1286,1253,1197,1178,1156,1057,976,882,851cm-1 |
I-1112 | mp86-87℃1H NMR(CDCl3)δ1.77(d,J=0.6Hz,3H),1.82(d,J=0.9Hz,3H),2.27(s,6H),4.65(d,J=6.6Hz,2H),5.00(s,1H),5.55(m,1H),6.86-6.92(m,2H),6.98(d,J=8.4Hz,1H),7.10(s,1H),7.11(s,1H),7.20(dd,J=2.1,8.4Hz,1H),7.22-7.26(m,2H),7.38(d,J=2.1Hz,1H)IR(KBr)3339,1608,1530,1492,1429,1362,1288,1258,1232,1213,1189,1112,889,783cm-1 |
I-1113 | amorphous1H NMR(CDCl3)δ1.76(s,3H),3.32(s,6H),3.44(s,3H),3.74(s,3H),5.23(s,2H),7.02(s,1H),7.14-7.20(m,2H),7.28(d,J=8.7Hz,1H),7.32-7.55(m,7H),7.72(d,J=8.4Hz,2H),9.22(s,1H),IR(KBr)3382,1684,1518,1469,1365,1237,1150,1017,972,872,815cm-1 |
I-1114 | mp173-175℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),1.97(s,3H),3.19(s,6H),3.21(s,3H),3.37(s,3H),3.75(s,3H),4.62(d,J=6.9Hz,2H),5.50(t,J=6.9Hz,1H),6.85(m,2H),7.06(d,J=8.4Hz,1H),7.25(m,1H),7.37(brs,1H),7.66(d,J=8.7Hz,2H)IR(KBr)3421,1518,1470,1366,115,1107,970,814cm-1 |
I-1115 | mp96-98℃1H NMR(DMSO-d6)δ1.72(s,3H),1.77(s,3H),3.27(s,3H),3.59(s,3H),4.21(s,2H),4.55(d,J=6.3Hz,2H),5.50(t,J=6.3Hz,1H),6.17(s,1H),6.59(dd,J=8.1,1.8Hz,1H),6.66(d,J=1.8Hz,1H),6.82(d,J=8.7Hz,2H),6.97(d,J=8.1Hz,1H),7.42(d,J=8.7Hz,2H),8.89(brs,1H),9.45(brs,1H)IR(KBr)3431,3396,3319,1611,1521,1486,1264,1172,1111,987,826cm-1 |
I-1116 | mp186-188℃1H NMR(DMSO-d6)δ1.72(s,3H),1.76(s,6H),3.28(s,3H),3.68(s,3H),4.54(d,J=6.6Hz,2H),5.48(t,J=6.6Hz,1H),6.53-6.58(m,1H),6.65(d,J=1.8Hz,1H),6.83-6.89(m,4H),7.43(d,J=8.4Hz,2H),8.73(brs,1H),8.96(brs,1H),9.53(brs,1H)IR(KBr)3429,1652,1611,1519,1474,1250,1080,1018,981,836cm-1 |
I-1117 | mp210-213℃1H NMR(CDCl3)δ3.48(s,3H),3.77(s,3H),5.16(s,2H),5.71(s,1H),5.85(s,1H),6.48(s,1H),6.95(dd,J=8.4,2.1Hz,1H),7.04(d,J=8.4Hz,1H),7.07(d,J=2.1Hz,1H),7.40-7.48(m,5H),7.83(d,J=9.0Hz,2H),8.32(d,J=9.0Hz,2H)IR(KBr)3499,1511,1343,1284,1247,1195,1109,1070,1013cm-1 |
I-1118 | mp156-158℃1HNMR(CDCl3)δ2.67(s,3H),3.14(s,3H),3.56(s,3H),3.80(s,3H),5.20(s,2H),6.87(s,1H),7.16(d,J=8.7Hz,1H),7.32-7.48(m,7H),7.82(d,J=9.2Hz,2H),8.32(d,J=9.2Hz,2H)IR(KBr)1518,1479,1350,1177,1119,1079,947,816cm-1 |
I-1119 | mp173-175℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.71(s,3H),3.24(s,3H),3.57(s,3H),3.80(s,3H), 4.64(d,J=6.7Hz,2H),5.50(t,J=6.7Hz,1H),6.87(s,1H),7.10(d,J=8.4Hz,1H),7.35(d,J=8.4,2.1Hz,1H),7.39(d,J=2.0Hz,1H),7.82(d,J=9.0Hz,2H),8.32(d,J=9.0Hz,2H)IR(KBr)1519,1479,1360,1178,1075,946,850,799cm-1 |
I-1120 | mp191-193℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),3.48(s,3H),3.77(s,3H),4.63(d,J=6.6Hz,2H),5.53(t,J=6.6Hz,1H),5.72(s,1H),5.83(s,1H),6.48(s,1H),6.93(dd,J=8.1,1.8Hz,1H),6.98(d,J=8.1Hz,1H),7.04(d,J=1.8Hz,1H),7.83(d,J=9.0Hz,2H),8.32(d,J=9.0Hz,2H)IR(KBr) 3492,1588,1511,1482,1345,1283,1244,1116,1069,1010cm-1 |
I-1121 | mp135-138℃1H NMR(CDCl3)δ1.76(s,3H),1.82(3,3H),3.61(s,3H),3.67(s,3H),3.73(s,3H),4.62(d,J=6.9Hz,2H),5.00(br.s,1H),5.50-5.57(m,1H),5.69(br,s,1H),6.65(s,1H),6.86-6.96(m,4H),7.00(d,J=1.8Hz,1H),7.48(d,J=8.4Hz,2H)IR(KBr)3428,2938,1680,1613,1594,1520,1479,1460,1393,1260,1226,1104,1081,993,834cm-1 |
I-1122 | mp140-142℃1H NMR(CDCl3)δ1.78(s,3H),1.82(s,3H),2.34(s,3H),4.65-4.67(d,J=6.9Hz,2H),5.55(m,1H),6.41-6.78(dt,JF-H=54.6,3.3Hz,2H),7.05-7.25(m,5H),7.26-7.45(m,2H),7.75(m,2H)IR(CHCl3)1752,1523,1493,1435,1385,1301,1272,1169,1132,1070,1037,916,889cm-1 |
I-1123 | mp178-180℃1H NMR(CDCl3)δ1.75(s,3H),1.78-1.79(d,d=0.6Hz,3H),2.13(s,3H),3.50(s,3H),3.87(s,3H),4.63-4.65(d,J=6.6Hz,2H),5.00(br,1H),5.57(m,1H),5.75(s,1H),6.79(s,1H),6.84-7.00(m,5H),7.50-7.53(m,2H)IR(CHCl3)3596,3528,2937,1612,1584,1522,1489,1454,1400,1259,1173,1139,1102,1009,930,865,835cm-1 |
I-1124 | mp173-174℃1H NMR(CDCl3)δ3.03(s,6H),3.54(s,3H),3.76(s,3H),3.91(s,3H),5.22(s,2H),6.80-6.99(m,6H),7.28-7.58(m,7H)IR(CHCl3)2938,1731,1609,1527,1485,1442,1394,1365,1174,1141,1082,1037,1013,961,936,863cm-1 |
I-1125 | mp103-106℃1H NMR(CDCl3)δ1.78(s,3H),1.82-1.83(d,J=0.9Hz,3H),4.65-4.67(d,J=6.9Hz,2H),5.55(m,1H),6.41-6.78(td,JF-H=54.9,2.7Hz,2H),6.94-7.31(m,7H),7.73(m,2H)IR(CHCl3)3592,1612,1525,1495,1385,1301,1263,1187,1173,1132,1069,1036,917,889,838cm-1 |
I-1126 | mp153-155℃1H NMR(CDCl3)δ1.75(s,3H),1.78-1.79(d,J=0.9Hz,3H),2.58(s,3H),3.03(s,6H),3.55(s,3H),3.77(s,3H),3.88(s,3H),4.61-4.64(d,J=6.9Hz,2H),5.54(m,1H),6.80-6.97(m,6H),7.54-7.57(d,J=8.7Hz,2H)IR(CHCl3)2938,1609,1527,1485,1464,1442,1392,1365,1174,1140,1082,1038,1012,961,935cm-1 |
I-1127 | mp160-161℃1HNMR(CDCl3)δ2.12(s,3H),3 49(s,3H),3.89(s,3H),4.89(br,1H),5.21(s,2H),5.76(s,1H),6.79-6.92(m,5H),7.00(d,J=8.4Hz,1H),7.31-7.53(m,7H)IR(CHCl3)3594,3517,2937,1731,1612,1589,1522,1489,1455,1400,1327,1259,1240,1173,1139,1102,1011,930,865,835cm-1 |
I-1128 | mp149-150℃1H NMR(CDCl3)δ1.74-1.75(d,J=0.9Hz,3H),1.78-1.79(d,J=0.9Hz,3H),3.03(s,1H),3.49(s,6H),3.75(s,3H),3.88s,3H),4.62-4.64(d,J=6.6Hz,2H),5.57(m,1H),5.95(s,1H),6.49(s,1H),6.81-6.84(m,2H),6.95-7.03(m,3H),7.55-7.58(m,2H)IR(CHCl3)3509,2937,1675,1610,1584,1528,1492,1464,1397,1362,1323,1197,1175,1140,1117,1078,1038,1011,929,835cm-1 |
I-1129 | mp163-165℃1H NMR(CDCl3)δ2.15(s,3H),2.47(s,3H),3.20(s,3H),3.55(s,3H),3.90(s,3H),5.22(s,2H),6.80(dd,J=8.4,2.1Hz,1H),6.88(d,J=2.1Hz,1H),7.00(d,J=8.4Hz,1H),7.17(s,1H),7.35-7.47(m,7H),7.66-7.69(m,2H)IR(CHCl3)2938,1604,1584,1518,1478,1370,1331,1241,1176,1150,1010,987,937,872,846cm-1 |
I-1130 | mp142-144℃1H NMR(CDCl3)δ1.76-1.77(d,J=0.9Hz,3H),1.79-1.80(d,J=0.9Hz,3H),2.16(s,3H),2.60(s,3H),3.20(s,3H),3.57(s,3H),3.88(s,3H),4.62-4.65(d,J=6.6Hz,2H),5.55(m,1H),6.83-6.87(m,2H),7.00(d,J=8.4Hz,1H),7.18(s,1H),7.35-7.38(m,2H),7.67-7.70(m,2H)IR(CHCl3)1604,1582,1517,1478,1416,1370,1332,1240,1176,1150,1093,1008,987,936,872cm-1 |
I-1131 | mp121-123℃1H NMR(DMSO-d6)δ1.70(s,3H),1.71(s,3H),3.71-3.75(m,4H),3.75(s,6H),5.21-5.27(m,2H),5.54-5.59(m,2H),6.65-6.71(m,2H),6.95(s,2H),7.19-7.29(m,4H)IR(KBr)3600-2800(br),1627,1536,1497,1470,1454,1375,1341,1257,1208,1125,1053,1035cm-1 |
I-1132 | mp169-170℃1H NMR(CDCl3)δ1.77(d,J=0.6Hz,3H),1.81(d,J=0.9Hz,3H),2.26(s,6H),4.63(d,J=6.6Hz,2H),5.31(s,1H),5.34(s,1H),5.55(m,1H),6.80(dd,J=2.1,8.1Hz,1H),6.89(d,J=2.1Hz,1H),6.92(d,J=8.1Hz,1H),6.98-7.13(m,5H)IR(KBr)3338,1619,1595,1523,1492,1475,1451,1427,1385,1357,1309,1298,1270,1223,1193,1172,1122,1113,999,983,871,819,785cm-1 |
I-1133 | mp135-136℃1H NMR(CDCl3)δ1.14(t,J=6.9Hz,3H),2.42(s,3H),3.20(s,3H),3.73(q,J=6.9Hz,2H),3.77(s,3H),3.91(s,3H),5.22(s,2H),6.84(s,1H),6.91(dd,J=1.8,8.4Hz,1H),6.98(d,J=8.4Hz,1H),6.98(d,J=1.8Hz,1H),7.28-7.47(m,7H),7.68-7.73(m,2H)IR(KBr)1516,1481,1381,1363,1332,1238,1228,1175,1147,1080,1036,865,843,800cm-1 |
I-1134 | mp154-155℃1H NMR(CDCl3)δ1.15(t,J=7.2Hz,3H),1.75(d,J=0.9Hz,3H),1.79(d,J=0.9Hz, 3H),2.54(s,3H),3.21(s,3H),3.72(q,J=7.2Hz,2H),3.78(s,3H),3.88(s,3H),4.63(d,J=6.9Hz,2H),5.54(m,1H),6.85(s,1H),6.95-6.98(m,3H),7.34-7.40(m,2H),7.68-7.74(m,2H)IR(KBr)1519,1481,1467,1365,1335,1245,1231,1184,1157,1081,1038,972,889,872,840,800cm-1 |
I-1135 | mp136-137℃1HNMR(CDCl3)δ1.16(t,J=6.9Hz,3H),1.74(s,3H),1.78(s,3H),3 61(q,J=6.9Hz,2H),3.75(s,3H),3.88(s,3H),4.63(d,J=6.9Hz,2H),5.03(s,1H),5.57(m,1H),5.99(s,1H),6.46(s,1H),6.89-6.94(m,2H),6.97(d,J=8.7Hz,1H),7.01(d,J=1.8Hz,1H),7.02(dd,J=1.8,8.7Hz,1H),7.51-7.57(m,2H)IR(KBr)3433,1613,1522,1489,1464,1443,1402,1383,1364,1270,1235,1214,1174,1140,1113,1072,1036,983,825cm-1 |
I-1136 | mp155-157℃1H NMR(CDCl3)δ2.05(t,J=2.7Hz,1H),2.76(dt,J=6.3,2.7Hz,2H),2.77(s,3H),3.21(s,3H),3.28(s,3H),3.56(s,3H),3.78(s,3H),4.23(t,J=6.3Hz,2H),6.84(s,1H),7.09(d,J=84Hz,1H),7.36(dd,J=8.4,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)3285,1608,1519,1176,1151,1119,1079,970,870,815,797cm-1 |
I-1137 | 泡沫1H NMR(CDCl3)δ1.83(s,3H),2.58(t,J=6.6Hz,2H),2.74(s,3H),3.21(s,3H),3.22(s,3H),3.56(s,3H),3.78(s,3H),4.22(t,J=6.6Hz,2H),4.84(brs,1H),4.89(brs,1H),6.84(s,1H),7.10(d,J=8.4Hz,1H),7.32~7.43(m,4H),7.68(d,J=8.7Hz,2H),IR(Nujol)1608,1519,1176,1150,1119,1078,968,869,816cm-1 |
I-1138 | 泡沫1H NMR(CDCl3)δ1.81(s,3H),2.55(t,J=6.6Hz,2H),3.45(s,3H),3.74(s,3H),4.20(t,J=6.6Hz,2H),4.85(brs,1H),4.89(brs,1H),6.45(s,1H),686~7.07(m,5H),7.53(d,J=8.7Hz,2H),IR(Nujol)3531,3328,1612,1587,1523,1489,1287,1226,1115,1072,1011cm-1 |
I-1139 | 泡沫1H NMR(CDCl3)δ2.07(t,J=2.7Hz,1H),2.72(dt,J=6.6,2.7Hz,2H),3 45(s,3H),3.75(s,3H),4.21(t,J=6.6Hz,2H),6.45(s,1H),6.87~7.10(m,5H),7.53(d,J=8.7Hz,2H)IR(Nujol)3482,3305,109,1597,1527,1494,1253,1240,1227,1127,1118,1079,1010cm-1 |
I-1140 | m.p194-197℃1H NMR(DMSO)δ3.29(s,3H),3.64(s,3H),5.42(s,2H),6.38(s,1H),6.61(dd,J=2.0,8.2Hz,1H),6.74(d,J=2.0Hz,1H),6.84(d,J=8.6Hz,2H),6.96(d,J=8.2Hz,1H),7.19(d,J=7.8Hz,1H),7.41(d,J=7.8Hz,1H),7.43(d,J=8.4Hz,2H)IR(KBr)3432,1611,1566,1523,1488,1430,1400,1380,1241,1113,1071,814cm-1 |
I-1141 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),d3.75(s,3H),3.92(s,3H),5.53(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.94(dd,J=2.1,8.7Hz,1H),7.01(d,J=8.7Hz,1H),7.10(d,J=2.1Hz,1H),7.28(d,J=4.8Hz,1H),7.52(d,J=4.8Hz,1H),7.53(d,J=8.4Hz,2H)IR(KBr)3423,1702,1684,1611,1523,1489,1439,1402,1282,1112,1073,1010,814cm-1 |
I-1142 | 泡沫1H NMR(CDCl3)δ2.74(s,3H),3.21(s,3H),3.22(s,3H),3.55(s,3H),d3.78(s,3H),3.91(s,3H),5.19(s,2H),6.60(d,J=3.6Hz,1H),6.84(s,1H),7.15(d,J=8.4Hz,1H),7.17(d,J=3.6Hz,1H),7.36(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.41(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1728,1519,1481,1365,1177,1150,1079,969,876,797cm-1 |
I-1143 | 泡沫1H NMR(CDCl3)δ2.77(s,3H),3.21(s,3H),3.23(s,3H),3.56(s,3H),d3.78(s,3H),4.18(m,2H),4.78(m,2H),5.94(m,2H),6.84(s,1H),7.11(d,J=8.4Hz,1H),7.36(dd,J=2.1,8.4Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1609,1519,1481,1367,1177,1150,1079,970,876,797cm-1 |
I-1144 | 泡沫1H NMR(CDCl3)δ2.75(s,3H),3.21(s,3H),3.24(s,3H),3.55(s,3H),d3.78(s,3H),4.11(m,2H),4.64(m,2H),6.05(t,J=4.5Hz,1H),6.06(t,J=5.1Hz,1H),6.84(s,1H),7.07(d,J=8.7Hz,1H),7.35(dd,J=2.1,8.7Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)1609,1519,1481,1364,1177,1151,1079,969,874,797cm-1 |
I-1145 | m.p203-205℃1H NMR(CDCl3)δ2.83(s,3H),3.22(s,3H),3.25(s,3H),3.55(s,3H),d3.79(s,3H),4.30(t,J=1.8Hz,2H),4.88(t,J=1.8Hz,2H),6.84(s,1H),7.20(d,J=8.7Hz,1H),7.37(dd,J=2.1,8.7Hz,1H),7.39(d,J=8.7Hz,2H),7.42(d,J=2.1Hz,1H),7.67(d,J=8.7Hz,2H)IR(KBr)3443,1606,1519,1481,1360,1179,1150,1079,877,798cm-1 |
I-1146 | m.p173-174℃1H NMR(CD3OD)δ3.38(s,3H),3.68(s,3H),4.23(t,J=1.8Hz,2H),4.83(t,J=1.8Hz,2H),6.43(s,1H),6.79(dd,J=2.1,8.1Hz,1H),6.85(d,J=8.7Hz,2H),6.86(d,J=2.1Hz,1H),7.04(d,J=8.1Hz,1H),7.45(d,J=8.7Hz,2H)IR(KBr)3399,1612,1586,1523,1487,1401,1217,1114,1067,1013,996,828cm-1 |
I-1147 | 泡沫1H NMR(CDCl3)δ3.39(s,3H),3.45(s,3H),3.74(s,3H),4.17(t,J=1.8Hz,2H),4.83(t,J=1.8Hz,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.97(dd,J=2.1,8.1Hz,1H),7.05(d,J=8.1Hz,1H),7.08(d,J=2.1Hz,1H),7.52(d,J=8.7Hz,2H)IR(KBr)3411,1612,1589,1523,1489,1404,1224,1114,1071,1010,939,816cm-1 |
I-1148 | 泡沫1H NMR(CDCl3)δ1.14(t,J=7.5Hz,3H),2.23(q,J=7.5Hz,2H),2.71(s,3H),3.21(s,3H),3.27(s,3H),3.60(s,3H),3.78(s,3H),4.80(s,2H),6.84(s,1H),7.20(d,J=9.0Hz,1H),7.37(dd,J=2.1,9.0Hz,1H),7.38(d,J=8.7Hz,2H),7.42(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(KBr)2232,1609,1519,1481,1365,1177,1151,1079,970,876,797cm-1 |
I-1149 | mp>280℃(decomp.)1H NMR(DMSO-d6)δ3.30(s,3H),3.64(s,3H),4.85(s,2H),6.39(s,1H),6.69(dd,J=8.4,2.1Hz,1H),6.79(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),6.94(d,J=8.4Hz,1H),7.44(d,J=8.7 Hz,2H),8.54(s,1H)IR(Nujol)3166,1707,1671,1611,1586,1523,1489,1288,1259,1211,1115,1075,1012,814cm-1 |
I-1150 | 泡沫1HNMR(CDCl3)δ1.91(s,3H),3.45(s,3H),3.75(s,3H),4.80(s,2H),5.29(brs,1H),5.36(brs,1H),6.45(s,1H),6.02(d,J=8.7Hz,2H),6.97(dd,J=8.4,2.1Hz,1H),7.07(d,J=8.4Hz,1H),7.08(d,J=2.1Hz,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3432,1612,1588,1523,1489,1288,1224,1192,1113,1070,1010,938,825,813cm-1 |
I-1151 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.98(d,J=1.8Hz,2H),5.92 (dt,J=7.5,1.8Hz,1H),6.45(s,1H),6.46(d,J=7.5Hz,1H),6.92(d,J=8.7Hz,2H),6.98(dd,J=8.4,2.1Hz,1H),7.09(d,J=2.1Hz,1H),7.11(d,J=8.4Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3410,1612,1589,1523,1489,1403,1224,1112,1070,1011,938,826cm-1 |
I-1152 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.89(d,J=2.1Hz,2H),5.97(dt,J=13.8,2.1Hz,1H),6.45(s,1H),6.61(d,J=13.8Hz,1H),6.92(d,J=8.7Hz,2H),6.97(dd,J=8.4,2.1Hz,1H),7.04(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3427,1612,1588,1523,1489,1403,1226,1192,1175,1113,1070,1011,938,918,826cm-1 |
I-1153 | mp188-189℃1H NMR(CDCl3)δ2.84(s,3H),3.33(s,3H),3.74(s,3H),3.98(s,3H),4.18(s,3H),6.38(s,2H),7.05(s,1H),7.36-7.64(m,10H),8.61(d,J=8.7Hz,1H),8.82(brs,1H)IR(KBr)3381,2942,1724,1538,1481,1369,1296,1177,1163,1082,963,821cm-1 |
I-1154 | mp78-80℃1H NMR(CDCl3)δ2.17(s,3H),2.67(s,3H),3.13(s,3H),3.57(s,3H),3.79(s,3H),5.19(s,2H),6.83(s,1H),7.15(d,J=8.6Hz,1H),7.31-7.45(m,7H),7.62(d,J=8.2Hz,1H),7.79(s,1H),8.44(d,J=8.6Hz,1H),8.51(brs,1H)IR(KBr)3398,2939,1739,1529,1477,1368,1287,1240,1177,1119,1078,957,815,796,522cm-1 |
I-1155 | mp74-75℃1H NMR(CDCl3)δ1.68(s,3H),176(s,6H),1.81(s,3H),2.69(s,3H),3.24(s,3H),3.52(s,3H),3.80(s,3H),3.88(s,3H),3.88-4.02(m,2H),4.64(d,J=7.2Hz,2H),5.25(t,J=7.8Hz,1H),5.50(t,J=5.7Hz,1H),6.88(s,1H),7.08-7.38(m,6H)IR(KBr) 3412,2939,1697,1519,1483,1366,1268,1207,1178,1080,964,808,523cm-1 |
I-1156 | mp72-74℃1H NMR(CDCl3)δ1.95(s,3H),1.99(s,3H),2.87(s,3H),3.42(s,3H),3.74(s,3H),3.97(s,3H),4.16(s,3H),4.82(d,J=6.6Hz,2H),5.68(t,J=5.7Hz,1H),7.04(s,1H),7.27(d,J=8.1Hz,1H),7.39-7.66(m,4H),8.60(d,J=8.4Hz,1H),8.81(brs,1H)IR(KBr) 3407,2940,1731,1601,1538,1481,1366,1294,1178,1165,1079,805,562cm-1 |
I-1157 | mp68-69℃1H NMR(CDCl3)δ1.70(s,3H),1.77(s,3H),1.81(s,3H),2.70(s,3H),3.25(s,3H),3.55(s,3H),3.81(s,3H),4.64(d,J=6.6Hz,2H),5.27(t,J=7.5Hz,1H),5.50(t,J=6.9Hz,1H),6.86(s,1H),7.10(d,J=8.4Hz,1H),7.25-7.40(m,3H),7.57(d,J=8.1Hz,1H),7.76(s,1H)IR(KBr)3422,2939,1701,1519,1480,1368,1203,1177,1078,957,801,522cm-1 |
I-1158 | mp64-66℃1H NMR(CDCl3)δ3.47(s,3H),3.74(s,3H),5.19(s,2H),5.86(brs,1H),6.44(s,1H),7.08-7.69(m,1H),8.06(brs,1H)IR(KBr)3399,2938,1726,1624,1604,15263,1487,1403,1302,1208,1178,1068,695,520cm-1 |
I-119 | mp68-70℃1H NMR(CDCl3)δ2.57(s,3H),3.57(s,3H),3.76(s,3H),5.21(s,2H),6.84(s,1H),7.11-7.73(m,11H),8.29(brs,1H)IR(KBr)3422,2939,1728,1605,1523,1482,1397,1367,1233,1209,1178,1078,795,725,542cm-1 |
I-1160 | mp72-73℃1H NMR(CDCl3)δ1.75(s,6H),1.78(s,3H),1.82(s,3H),3.48(s,3H),3.75(s,3H),3.76(d,J=7.2Hz,2H),3.89(s,3H),4.38(brs,1H),4.61(d,J=6.9Hz,2H),5.41(t,J=6.3Hz,1H),5.53(t,J=6.9Hz,1H),5.68(brs,1H),5.94(brs,1H),6.49(s,3H),6.69(d,J=8.4Hz,1H),6.95(s,1H),7.06(s,1H),7.13-7.15(m,2H),7.26(s,1H)IR(KBr)3423,2932,1608,1528,1490,1459,1250,1113,1071,805,757cm-1 |
I-1161 | mp68-69℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.48(s,3H),3.75(s,3H),3.91(s,3H),4.61(d,J=7.2Hz,2H),5.53(t,J=6.0Hz,1H),5.91(brs,2H),6.47(s,1H),6.83(d,J=8.1Hz,2H),6.95(s,1H),7.06-7.09(m,2H),7.16(s,1H),7.26(s,1H)IR(KBr)3406,2933,1524,1490,1397,1270,1241,1116,1075,1069,811,773cm-1 |
I-1162 | mp81-83℃1H NMR(CDCl3)δ1.76(s,6H),1.79(s,3H),1.81(s,3H),3.50(s,3H),3.75(s,3H),3.80(d,J=6.6Hz,2H),4.36(brs,1H),4.61(d,J=6.9Hz,2H),5.39(t,J=6.3Hz,1H),5.53(t,J=6.6Hz,1H),5.68(brs,1H),5.90(brs,1H),6.43(s,1H),6.73(d,J=8.4Hz,1H),6.95(s,1H),7.05(s,1H),7.26(d,J=0.9Hz,1H),7.47(dd,J=2.1,8.4Hz,1H),7.59(d,J=2.1Hz,1H)IR(KBr)3484,2931,1607,1525,1488,1310,1243,1114,1070,1009,808cm-1 |
I-1163 | mp87-89℃1H NMR(CDCl3)δ2.81(s,3H),3.60(s,3H),3.77(s,3H),3.98(d,J=6.3Hz,2H),4.80(d,J=6.3Hz,2H),6.07(t,J=6.0Hz,1H),6.25(t,J=6.3Hz,1H),6.46-6.53(m,2H),6.86(s,1H),7.05-7.38(m,4H)IR(KBr)3411,2937,1628,1527,1482,1364,1233,1176,1077,960,879,792,524cm-1 |
I-1164 | 无定形1H NMR(CDCl3)δ2.68(s,3H),3.13(s,3H),3.43(s,3H),3.54(s,3H),3.80(s,3H),5.19(s,2H),6.87(s,1H),7.16(d,J=8.7Hz,1H),7.32-7.49(m,9H),7.69(d,J=8.4Hz,2H)IR(KBr)1698,1522,1482,1367,1080,1014,947,815,795cm-1 |
I-1165 | 泡沫1H NMR(CDCl3)δ1.47(s,3H),172(s,3H),1.77(s,3H),1.81(s,3H),2.71(s,3H),3.24(s,3H),3.51(s,3H),3.80(s,3H),4.37(d,J=7.8Hz,2H),4.64(d,J=6.6Hz,2),5.29(t,J=7.8Hz,1H),5.50(t,J=6.6Hz,1H),6.88(s,1H),7.09(d,J=8.4Hz,1H),7.27(d,J=8.7Hz,2H),7.35(dd,J=8.4,2.3Hz,1H),7.39(d,J=2.3Hz,1H),7.66(d,J=8.7Hz,2H)IR(KBr)1696,1521,1482,1366,1177,1080,972,946,814,795cm-1 |
I-1166 | mp135-136℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.71(s,3H),3.24(s,3H),3.54(s,3H),3.80(s,3H),4.64(d,J=6.7Hz,2H),5.50(t,J=6.7Hz,1H),6.87(s,1H),7.10(d,J=8.4Hz,1H),7.34(d,J=8.1Hz,2H),7.35(dd,J=8.4,2.2Hz,1H),7.39(d,J=2.2Hz,1H),7.69(d,J=8.1Hz,2H)IR(KBr)1702,1522,1481,1362,1275,1150,1081,1014,978,817,793cm-1 |
I-1167 | mp169-171℃1H NMR(DMSO-d6)δ1.71(s,3H),1.72(s,6H),1.76(s,3H),3.31(s,3H),3.63(s,3H),3.64(m,2H),4.54(d,J=6.8Hz,2H),5.29(t,J=7.5Hz,1H),5.49(t,J=6.8Hz,1H),5.75(t,J=8.1Hz,1H),6.37(s,1H),6.63(d,J=8.4Hz,2H),6.64(dd,J=8.1,2.0Hz,1H),6.73(d,J=2.0Hz,1H),6.88(d,J=8.4Hz,2H),7.37(d,J=8.4Hz,2H),8.41(s,1H),8.70(s,1H)IR(KBr)3473,3276,1608,1523,1491,1310,1252,1190,1112,1072,934,824,776cm-1 |
I-1168 | mp159-160℃1H NMR(DMSO-d6)δ1.72(s,3H),1.76(s,3H),3.31(s,3H),3.64(s,3H),4.54(d,J=6.8Hz,2H),5.49(t,J=6.8Hz,1H),5.76(brs,1H),6.37(s,1H),6.61(d,J=8.4Hz,2H),6.64(dd,J=8.1,2.0Hz,1H),6.73(d,J=2.0Hz,1H),6.88(d,J=8.1Hz,1H),7.39(d,J=8.4Hz,2H),7.37(d,J=8.4Hz,2H),8.42(brs,1H),8.70(brs,1H)IR(KBr)3458,3332,1609,1524,1492,1411,1393,1295,1234,1107,1071,1012,994,781cm-1 |
I-1169 | mp183-184℃1H NMR(CDCl3)δ1.76(d,J=0.6Hz,3H),1.82(s,3H),3.13(s,3H),3.48(s,3H),3.76(s,3H),4.63(d,J=6.9Hz,2H),5.53(m,1H),5.72(s,1H),5.83(s,1H),6.46(s,1H),6.93(dd,J=1.8,8.4Hz,1H),6.98(d,J=8.4Hz,1H),7.04(d,J=1.8Hz,1H),7.82-7.89(m,2H),8.00-8.06(m,2H)IR(KBr)3445,1593,1499,1482,1461,1387,1311,1278,1245,1189,1146,1111,1086,1068,1010,997,942,766cm-1 |
I-1170 | mp178-179℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.80(s,3H),3.47(s,3H),3.76(s,3H),4.62(d,J=7.2Hz,2H),5.53(m,1H),5.72(s,1H),5.86(s,1H),6.47(s,1H),6.94(dd,J=1.8,8.1Hz,1H),6.98(d,J=8.1Hz,1H),7.05(d,J=1.81Hz,1H),7.72-7.77(m,2H),7.79-7.85(m,2H)IR(KBr)3420,1587,1527,1482,1449,1430,1416,1390,1357,1290,1240,1214,1198,1135,1115,1073,1019,998,975,962,937,831cm-1 |
I-1171 | mp136-139℃1H NMR(CDCl3)δ1.73(s,3H),1.77(s,3H),2.99(s,6H),3.71(d,J=6.6Hz,2H),3.76(s,3H),3.78(s,3H),5.32-5.37(m,1H),6.36-6.46(m,2H),6.79-6.84(m,2H),6.89(s,H),6.95(s,1H),7.18-7.24(m,H),7.47-7.52(m,2H)IR(KBr)3600-2800(br),1626,1609,1531,1493,1460,1444,1388,1345,1232,1207,1173,1124,1050,1028cm-1 |
I-1172 | mp113-114℃1H NMR(CDCl3)δ3.00(s,6H),3.77(s,3H),3.78(s,3H),6.78-6.84(m,2H),6.88(s,1H),6.98(s,1H),7.31(dd,J=2.1,8.4Hz,1H),7.43-7.53(m,3H),7.58(dd,J=1.8,11.1Hz,1H)IR(KBr)3600-2800(br),1711,1609,1533,1493,1464,1390,1212,1181,1162,1052,1027cm-1 |
I-1173 | mp141-143℃1H NMR(CDCl3)δ1.75(d,J=0.9Hz,3H),1.78(d,J=0.9Hz,3H),2.99(s,6H),3.50(s,3H),3.74(s,3H),3.78(d,J=6.6Hz,2H),3.93(br,1H),5.35-5.40(m,1H),5.86(s,1H),6.44(s,1H),6.74-6.86(m,3H),7.30-7.38(m,4H)IR(KBr)3600-2800(br),1625,1611,1530,1491,1458,1444,1400,1348,1333,1250,1217,1103,1075cm-1 |
I-1174 | mp226-228℃1H NMR(CDCl3)δ3.93(s,3H),4.95(s,1H),5.21(s,2H),6.90-6.94(m,2H),6.96(s,1H),6.97(s,1H),7.03(d,J=0.9Hz,1H),7.30-7.49(m,1H)IR(KBr)3600-2800(br),1608,1589,1520,1471,1446,1384,1358,1270,1250,1238,1210,1172,1141,1093,1031,997cm-1 |
I-1175 | mp143-145℃1H NMR(CDCl3)δ3.21(s,3H),3.93(s,3H),5.22(s,2H),6.97(s,2H),7.03(s,1H),7.30-7.55(m,11H)IR(KBr)3600-2800(br),1602,1517,1468,1368,1348,1248,1210,1176,1151,1095,1038,989cm-1 |
I-1176 | mp98-100℃1H NMR(CDCl3)δ1.76(s,3H),1.79(s,3H),3.21(s,3H),3.91(s,3H),4.65(d,J=6.9Hz,2H),5.53-5.58(m,1H),6.94-7.03(m,3H),7.23-7.41(m,2H),7.45(s,1H),7.49(s,1H),7.51-7.56(m,1H)IR(KBr)3600-2800(br),1604,1583,1519,1470,1449,1365,1250,1202,1177,1151,1095,1041,972cm-1 |
I-1177 | mp118-120℃1H NMR(CDCl3)δ1.76(s,3H),1.79(s,3H),3.91(s,3H),4.64(d,J=6.9Hz,2H),5.53-5.58(m,1H),6.88-7.02(m,5H),7.23-7.37(m,2H),7.44(s,1H),7.45(s,1H)IR(KBr)3600-2800(br),1626,1609,1526,1490,1429,1253,1187cm-1 |
I-1178 | mp161-164℃1H NMR(CDCl3)δ3.00(s,3H),3.79(s,3H),3.80(s,3H),6.78-6.83(m,2H),6.90(s,1H),6.97(s,1H),7.47-7.52(m,2H),7.71(d,J=1.8Hz,1H),8.37(d,J=8.7Hz,1H),8.46(brs,1H)IR(KBr)3600-2800(br),1716,1613,1532,1505,1487,1463,1384,1357,1280,1195,1172,1059,1033cm-1 |
I-1179 | mp135-137℃1H NMR(CDCl3)δ1.74(s,3H),1.78(s,3H),3.00(s,6H),3.78(s,3H),3.79(s,3H),4.29(d,J=6.6Hz,1H),5.35-5.40(m,1H),6.71(d,J=8.4Hz,1H),6.80-6.83(m,2H),6.90(s,1H),6.94(s,1H),7.38-7.42(m,1H),7.48-7.56(m,3H)IR(KBr)3600.2800(br),1612,1532,1495,1460,1444,1385,1365,1273,1257,1203,1059,1039,1029cm-1 |
I-1180 | 1H NMR(CDCl3)δ1.57(d,J=6.3Hz,3H),2.26(s,3H),2.28(s,3H),5.18(s,2H),5.22(q,J=6.3Hz,1H),7.02(d,J=8.4Hz,1H),7.12(s,1H),7.15(s,1H),7.23(d.d,J=8.4&2.1Hz,1H),7.30-7.51(m,10H)IR(KBr)3557,1605,1486,1370,1235,1177,1149,1078,1017cm-1 |
I-1181 | 1H NMR(CDCl3)δ1.66(s,6H),2.27(s,3H),2.28(s,3H),3.20(s,3H),4.22(s,1H),5.22(s,2H),7.06(d,J=8.4Hz,1H),7.12(s,1H),7.14(s,1H),7.23(d.d,J=8.4&2.1Hz,1H),7.30-7.51(m,10H)IR(KBr)3544,3441,1604,1512,1465,1367,1222,1173,1149cm-1 |
I-1182 | 1H NMR(CDCl3)δ1.28(t,J=7.2Hz,3H),2.26(s,3H),2.28(s,3H),2.70(q,J=7.2Hz,2H),3.20(s,3H),4.73(s,1H),6.82(d,J=8.4Hz,1H),7.03-7.11(m,2H),7.14(s,1H),7.15(s,1H),7.29-7.46(m,4H)IR(KBr)3510,1605,1515,1488,1369,1263,1177,1147,1117cm-1 |
I-1183 | 1H NMR(CDCl3)δ1.29(d,J=6.9Hz,6H),2.27(s,3H),2.28(s,3H),3.20(s,3H),3.27(qintet,J=6.9Hz,1H),4.76(s,1H),6.81(d,J=7.8Hz,1H),7.07(d.d,J=7.8&2.1Hz,1H),7.11(s,1H),7.15(s,1H),7.20(d,J=2.1Hz,1H),7.34(d,J=8.7Hz,2H),7.42(d,J=8.7Hz,2H),IR(KBr)3511,1606,1484,1355,1174,1151cm-1 |
I-1184 | 1H NMR(CDCl3)δ1.23(t,J=8.1Hz,3H),1.77(s,3H),1.82(s,3H),2.26(s,3H),2.29(s,3H),2.70(q,J=8.1Hz,2H),3.20(s,3H),4.58(d,J=6.6Hz,2H),5.48-5.57(m,1H),6.90(d,J=7.8Hz,1H),7.08-7.13(m,2H),7.16(s,2H),7.23-7.47(m,4H)IR(KBr)1605,1485,1369,1352,1236,1201,1174,1150,1133,1008cm-1 |
I-1185 | 1H NMR(CDCl3)δ1.23(t,J=7.5Hz,3H),1.76(s,3H),1.81(s,3H),2.27(s,3H),2.29(s,3H),2.70(q,J=7.5Hz,2H),4.57(d,J=6.6Hz,2H),4.79(brs,1H),5.49-5.58(m,1H),6.83-6.92(m,3H),7.08-7.19(m,4H),7.27(d,J=8.4Hz,2H)IR(KBr)3529,1608,1519,1487,1241,1136,1024cm-1 |
I-1186 | 1H NMR(CDCl3)δ1.23(d,J=1.8Hz,6H),1.76(s,3H),1.82(s,3H),2.27(s,3H),2.29(s,3H),3.20(s,3H),3.40(quintet,J=1.8Hz,1H),4.58(d,J=6.6Hz,2H),5.48-5.59(m,1H),6.90(d,J=7.8Hz,1H),7.10-7.44(m,8H)IR(KBr)1602,1468,1369,1232,1174,1151cm-1 |
I-1187 | 1H NMR(CDCl3)δ1.24(d,J=6.9Hz,6H),1.76(s,3H),1.81(s,3H),2.27(s,3H),2.29(s,3H),3.40(quintet,J=6.9Hz,1H),4.58(d,J=6.6Hz,2H),4.79(broad,s,1H),5.50-5.57(m,1H),6.84-6.93(m,3H),7.09-7.16(m,3H),7.00-7.28(m,3H)IR(KBr)3265,1607,1519,1486,1448,1383,1232,1170cm-1 |
I-1188 | 1H NMR(CDCl3)δ1.31(d,J=6.9Hz,6H),1.44(s,3H),1.67(s,3H),2.97(quintet,J=6.9Hz,1H),3.78(s,3H),3.80(s,3H),3.92(s,3H),4.20-4.30(broad,1H),5.17-5.30(m,1H),6.96(s,1H),6.99(s,1H),7.07-7.35(m,5H),7.52(d,J=8.1Hz,2H)IR(KBr)3422,1601,1529,1492,1462,1378,1341,1257,1203,1138,1028cm-1 |
I-1189 | 1H NMR(CDCl3)δ2.67(s,3H),3.13(s,3H),3.57(s,3H),3.79(s,3H),5.19(s,2H),6.84(s,1H),7.15(d,J=9.0Hz,1H),7.31-7.50(m,8H),7.55(d.d,J=12.0&1.8Hz,1H),8.34-8.41(m,1H)IR(KBr)3428,1740,1601,1535,1482,1366,1292,1238,1177,1164,1112,1079,1013cm-1 |
I-1190 | 1H NMR(CDCl3)δ1.48(s,3H),1.70(s,3H),1.77(s,3H),1.81(s,3H),2.70(s,3H),3.24(s,3H),3.55(s,3H),3.81(s,3H),4.09-4.20(m,1H),4.53- 4.68(m,3H),5.18-5.30(m,1H),5.43-5.54(m,1H),6.86(s,1H),7.06-7.51(m,6H)IR(KBr)1702,1521,1482,1367,1204,1177,1115,1080cm-1 |
I-1191 | 1H NMR(CDCl3)δ1.75(s,5H),1.78(s,3H),1.82(s,3H),3.49(s,3H),3.74(s,3H),3.79(d,J=6.3Hz,2H),4.61(d,J=6.6Hz,2H),5.32-5.43(m,1H),5.49-5.57(m,1H),5.68(s,1H),5.90(s,1H),6.44(s,1H),6.74-6.85(m,1H),6.95(s,2H),7.05(s,1H),7.29-7.38(m,2H)IR(KBr)3527,1524,1530,1491,1248,1221,1197,1125,1105,1072cm-1 |
I-1192 | 1H NMR(CDCl3)δ1.75(s,3H),1.78(s,3),3.49(s,3H),3.73(s,3H),3.78(d,J=6.9Hz,2H),5.32-5.43(m,1H),6.44(s,1H),6.73-6.97(m,4H),7.25-7.37(m,2H)IR(KBr)3551,3437,3310,1607,1529,1491,1463,1402,1362,1269,1255,1184,1099,1070,1013cm-1 |
I-1193 | 1H NMR(CDCl3)δ2.28(s,3H),2.30(s,3H),3.00(s,6H),5.16(s,2H),5.69(s,1H),6.80(d,J=8.7Hz,2H),6.84(d.d,J=8.1&2.1Hz,1H),6.98(d,J=8.1Hz,1H),6.99(d,J=2.1Hz,1H),7.12(s,1H),7.13(s,1H),7.27(d,J=8.7Hz,2H),7.34-7.50(m,5H)IR(KBr)1605,1525,1490,1417,1242,1199,1127,1006cm-1 |
I-1194 | mp174-175℃1H NMR(CDCl3)δ3.48(s,3H),3.78(s,3H),4.41(s,4H),5.17(s,2H),5.71(s,1H),5.88(s,1H),6.48(s,1H),6.94-7.50(m,18H),7.86(ABq,J=8.4Hz,4H)IR(KBr)3463,3409,1588,1519,1482,15455,1417,1385,1321,1285,1247,1154,1112,1096,1067,1015cm-1 |
I-1195 | mp165-167℃1H NMR(CDCl3)δ2.68(s,3H),3.14(s,3H),3.56(s,3H),3.81(s,3H),4.40(s,4H),5.20(s,2H),6.86(s,1H),7.09-7.50(m,18H),7.79(ABq,J=8.1Hz,4H)IR(KBr)3434,2938,1606,1596,1518,1478,1455,1368,1335,1293,1268,1239,1174,1157,1118,1079cm-1 |
I-1196 | mp176-178℃1H NMR(CDCl3)δ1.58(s,3H),1.66(s,3H),1.77(s,3H),1.81(s,3H),2.71(s,3H),3.24(s,3H),3.55(s,3H),3.64(m,2H),3.80(s,3H),4.28(t,J=6.0Hz,1H),4.64(d,J=6.9Hz,2H),5.10(m,1H),5.49(m,1H),6.86(s,1H),7.10(d,J=8.4Hz,1H),7.35(ds,J=2.1,8.4Hz,1H),7.39(d,J=2.1Hz,1H),7.87(ABq,J=8.7Hz,4H)IR(KBr)3434,3321,2939,1517,1477,1366,1325,1292,1269,1240,1176,1156,1120,1077cm-1 |
I-1197 | mp180-181℃1H NMR(DMSO)δ1.74(s,3H),1.77(s,3H),2.87(s,3H),3.36(s,3H),3.51(s,3H),3.79(s,3H),4.68(d,J=6.6Hz,2H),5.48(m,1H),7.10(s,1H),7.28-7.30(m,3H),7.45(bs,2H),7.87(ABq,J=8.7Hz,4H)IR(KBr)3340,3238,2939,1598,1518,1481,1362,1333,1291,1270,1239,1172,1161,1120,1076,1007cm-1 |
I-1198 | oil1H NMR(CDCl3)δ1.45(s,3H),1.66(s,3H),1.87(s,3H),2.24(s,3H),2.27(s,3H),2.30(s,3H),3.84(s,3H),3.92(s,3H),3.95-4.03(m,1H),4.50-4.58(m,1H),5.22-5.29(m,1H),6.87-6.99(m,4H),7.09-7.17(m,3H),7.80(s,1H),8.34-8.42(m,1H)IR(CHCl3)3673,3021,1685,1639,1525,1495,1406,1237,1128,1037cm-1 |
I-1199 | mp177-179℃1H NMR(CDCl3)δ1.45(s,6H),1.66(s,6H),1.87(s,6H),2.29(s,6H),3.85(s,6H),3.95-4.04(m,2H),4.50-4.59(m,2H),5.23-5.29(m,2H),6.90-6.95(m,4H),7.10-7.15(m,2H),7.19(s,2H)IR(KBr)2929,1661,1492,1405,1288,1214,1030,869,829cm-1 |
I-1200 | mp224-226℃1H NMR(CDCl3)δ2.88(s,3H),3.22(s,3H),3.54(s,3H),3.78(s,3H),6.43(s,1H),6.85(s,1H),7.01(d,J=8.4Hz,1H),7.20(dd,J=2.1,8.4Hz,1H),7.35-7.42(m,2H),7.65-7.72(m,2H),7.96(d,J=2.1Hz,1H),8.96(s,1H)IR(KBr)3441,3370,3024,2938,1729,1508,1481,1365,1177,1148,1085,884,798,524cm-1 |
I-1201 | 粉末1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.80(s,3H),3.21(s,3H),3.56(s,3H),3.79(s,3H),4.67(d,J=6.6Hz,2H),5.46-5.51(m,1H),6.84(s,1H),7.05(d,J=8.1Hz,1H),7.22-7.26(m,1H),7.36-7.41(m,2H),7.67-7.71(m,2H),8.35(d,J=1.8Hz,1H),9.24(s,1H)IR(KBr)3385,2937,1718,1532,1479,1362,1175,1152,1078,973,876,797,526cm-1 |
I-1202 | mp260-262℃1H NMR(DMSO)δ2.27(s,6H),3.87(s,6H),7.00(dd,J=1.8,8.1Hz,2H),7.10(d,J=1.8Hz,2H),7.21(s,2H),7.48(d,J=8.1Hz,2H),10.73(s,2H)IR(KBr)3392,3008,1719,1600,1542,1413,1297,1158,1032,905,627cm-1 |
I-1203 | mp143-144℃1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),3.61(s,3H),3.67(s,3H),3.73(s,3H),3.87(s,3H),4.62(d,J=6.9Hz,2H),5.50-5.58(m,1H),5.66(s,1H),6.86-7.02(m,5H),7.54(d,J=9Hz,2H)IR(KBr)3494,2935,1673,1609,1584,1519,1479,1456,1389,1284,1249,1178,1109,1081,1016,829,798cm-1 |
I-1204 | mp90-91℃1H NMR(CDCl3)δ1.72(s,3H),1.79(s,3H),2.26(s,6H),4.69(d,J=7.2Hz,2H),4.9-5.0(brs,1H),5.57(t,J=7.2Hz,1H),6.085-7.0(m,4H),7.10(d,J=8.7Hz,2H),7.23(d,J=8.7Hz,2H)IR(KBr)3253,3013,2979,2928,1676,1584,1521,1492,1232,1034,950,848,825cm-1 |
I-1205 | mp131-132℃1H NMR(CDCl3)δ1.73(s,3H),1.79(s,3H),3. 43(s,3H),3.76(s,3H),4.68(d,J=6.9Hz,2H),4.9-5.1(brs,1H),5.58(t,J=7.2Hz,1H),6.09(brs,1H),6.44(s,1H),6.92(d,J=8.4Hz,2H),7.0-7.1(m,2H),7.52(d,J=8.4Hz,2H)IR(KBr)3428,2951,2932,1671,1611,1523,1491,1402,1233,1111,1077,1027,969,833cm-1 |
I-1206 | mp191-192℃1H NMR(CDCl3)δ2.15(s,6H),3.22(s,3H),3.87(s,3H),5.18(ABq,J=12.0Hz,2H),6.74(dd,J=2.1,8.1Hz,1H),6.78(d,J=2.1Hz,1H),6.93(d,J=8.1Hz,1H),7.24(s,1H),7.30-7.50(m,9H)IR(KBr) 1528,1479,1453,1364,1326,1262,1243,1223,1209,1200,1176,1152,1137,963,870,846,754cm-1 |
I-1207 | mp108-109℃1H NMR(CDCl3)δ1.77(s,3H),1.82(d,J=0.6Hz,3H),2.27(s,3H),2.28(s,3H),4.56(d,J=6.6Hz,2H),4.89(s,1H),5.54(m,1H),6.86-6.92(m,2H),6.94-7.00(m,2H),7.12(s,1H),7.13(s,1H),7.22-7.27(m,2H),7.27-7.31(m,2H)IR(KBr)3349,1608,1520,1488,1439,1383,1287,1263,1235,1175,999,979cm-1 |
I-1208 | mp194-195℃1H NMR(CDCl3)δ2.14(s,3H),2.16(s,3H),3.87(s,3H),4.97(s,1H),5.17(ABq,J=12.6Hz,2H),6.74(dd,J=2.1,8.1Hz,1H),6.79(d,J=2.1Hz,1H),6.88-6.93(m,2H),6.93(d,J=8.1Hz,1H),7.17-7.22(m,2H),7.24(s,1H),7.29-7.49(m,5H)IR(KBr)3408,1611,1526,1479,1463,1455,1382,1263,1242,1225,1212,1143,997,751cm-1 |
I-1209 | mp183-184℃1H NMR(CDCl3)δ2.03(s,3H),2.07(s,3H),3.19(s,3H),3.80(brs,2H),3.89(s,3H),5.21(s,2H),6.63(s,1H),6.77(dd,J=2.1,8.1Hz,1H),6.83(d,J=2.1Hz,1H),7.02(d,J=8.1Hz,1H),7.29-7.52(m,9H)IR(KBr)3481,3391,1610,1511,1482,1370,1240,1212,1197,1173,1153,1137,1024,1007,870,844cm-1 |
I-1210 | mp133-134℃1H NMR(CDCl3)δ1.75(s,3H),1.80(s,3H),2.16(s,3H),2.17(s,3H),3.22(s,3H),3.85(s,3H),4.61(d,J=6.9Hz,2H),5.55(m,1H),6.74-6.79(m,2H),6.92(d,J=8.7Hz,1H),7.24(s,1H),7.39(s,4H)IR(KBr)1529,1516,1478,1371,1353,1328,1263,1242,1201,1176,1150,975,866,846,787cm-1 |
I-1211 | mp243-244℃1H NMR(DMSO-d6)δ1.91(s,3H),1.96(s,3H),3.77(s,3H),4.05(brs,2H),5.12(s,2H),6.40(s,1H),6.71(dd,J=1.8,8.1Hz,1H),6.77-6.84(m,3H),7.06-7.12(m,2H),7.16(d,J=8.1Hz,1H),7.32-7.52(m,5H),9.38(s,1H)IR(KBr)3378,3289,1609,1586,1518,1483,1454,1402,1267,1236,1207,1171,1136,1024,853,835,816,753,730,695cm-1 |
I-1212 | mp195-196℃1H NMR(CDCl3)δ1.75(s,3H),1.79(s,3H),2.15(s,3H),2.16(s,3H),3.85(s,3H),4.61(d,J=6.9Hz,2H),4.97(s,1H),5.55(m,1H),6.76-6.79(m,2H),6.89-6.94(m,3H),7.18-7.23(m,2H),7.24(s,1H)IR(KBr)3462,1611,1519,1479,1459,1431,1379,1271,1240,1228,1211,1137,983,835cm-1 |
I-1213 | IR(KBr)3275,1494,1462,1444,1387,1371,1232,1212,1183,1141cm-1 |
I-1214 | mp106-108℃1H NMR(CDCl3)δ2.24(s,3H),3.79(s,3H),4.72(br,1H),5.20(s,2H),6.72-7.18(m,8H),7.36-7.50(m,6H)IR(CHCl3)3596,1610,1523,1493,1465,1455,1388,1318,1298,1262,1173,1127,1038,834cm-1 |
I-1215 | mp108-110℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.25(s,3H),3.79(s,3H),4.63-4.65(d,J=7.2Hz,2H),5.56(s,2H),6.81(s,1H),6.87-7.18(m,6H),7.44-7.47(m,2H)IR(CHCl3)3596,2937,1610,1523,1493,1465,1446,1387,1297,1261,1173,1125,1038,993,834cm-1 |
I-1216 | mp121-122℃1H NMR(CDCl3)δ2.24(s,3H),3.79(s,3H),4.78-4.80(d,J=6.9Hz,2H),6.24(t,J=6.9Hz,1H),6.80(s,1H),6.87-7.19(m,6H),7.43-7.48(m,2H)IR(CHCl3)3596,1612,1523,1493,1464,1389,1300,1259,1173,1127,1038,886,834cm-1 |
I-1217 | mp163-165℃1H NMR(CDCl3)δ2.26(s,3H),2.28(s,3H),4.78(brs,1H),4.78(d,J=6.5Hz,2H),5.60(s,1H)6.23(t,J=6.5Hz,1H),6.83-6.92(m,4H),6.99(d,J=2.1Hz,1H),7.10(s,1H),7.11(s,1H),7.22-7.27(m,2H)IR(CHCl3)3597,3548,3027,3010,1613,1588,1522,1490,1218,1208,1171cm-1 |
I-1218 | 泡沫1H NMR(CDCl3)δ2.37(s,3H),3.39(s,3H),3.73(s,3H),5.15(s,2H),5.68(s,1H),5.92(s,1H),6.46(s,1H),6.71(dd,J=3.7,0.7Hz,1H),6.96(dd,J=8.4,2.1Hz,1H),7.03(d,J=8.4Hz,1H),7 09(d,J=2.1Hz,1H),7.26(dd,J=8.6,0.7Hz,2H),7.37-7.45(m,5H),7.60(dd,J=8.7,1.5Hz,1H),7.61(d,J=3.7Hz,1H),7.78(d,J=1.5Hz,1H),7.82(d,J=8.6Hz,1H),8.05(d,J=8.7Hz,1H)IR(KBr)3476,1457,1371,1254,1107,1131,1107,1011,814,685,581cm-1 |
I-1219 | mp217-219℃1H NMR(CDCl3)δ2.37(s,3H),2.69(s,3H),3.12(s,3H),3.47(s,3H),3.76(s,3H),5.18(s,2H),8.71(d,J=3.8Hz,1H),6.86(s,1H),7.15(d,J=8.4Hz,1H),7.26(d,J=8.7Hz,2H),7.32-7.48(m,7H),7.56(dd,J=8.7,1.8Hz,1H),7.61(d,J=3.8Hz,1H),7.78(d,J=1.8Hz,1H),7.82(d,J=8.7Hz,1H),8.05(d,J=8.7Hz,1H)IR(KBr)1366,1174,1079,963,814,685,586cm-1 |
I-1220 | mp208-210℃1H NMR(CDCl3)δ2.37(s,3H),2.72(s,3H),3.23(s,3H),3.47(s,3H),3.76(s,3H),4.63(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),6.71(d,J=3.8Hz,1H),6.86(s,1H),7.09(d,J=8.4Hz,1H),7.26(d,J=8.3Hz,2H),7.35(dd,J=8.4,2.1Hz,1H),7.40(d,J=2.1Hz,1H),7.56(dd,J=8.4,1.7Hz,1H),7.61(d,J=3.8 Hz,1H),7.78(d,J=1.7Hz,1H),7.82(d,J=8.3Hz,2H),8.05(d,J=8.7Hz,1H)IR(KBr)1466,1445,1365,1174,1116,1079,964,812,686,584cm-1 |
I-1221 | mp203-205℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.39(s,3H),2.69(s,3H),2.97(t,J=8.6Hz,2H),3.23(s,3H),3.50(s,3H),3.77(s,3H),3.98(t,J=8.6Hz,2H),4.63(d,J=6.6Hz,2H),5.49(t,J=6.6Hz,1H),6.80(s,1H),7.08(d,J=8.5Hz,1H),7.24-7.28(m,2H),7.33(dd,J=8.5,2.0Hz,1H),7.37-7.39(m,2H),7.41-7.45(m,1H),7.71(d,J=8.4Hz,1H),7.73(d,J=8.1Hz,2H)IR(KBr)1474,1362,1241,1166,1079,975,808cm-1 |
I-1222 | 无定形1H NMR(CDCl3)δ1.76(s,3H),1.82(s,3H),2.39(s,3H),2.98(t,J=8.4Hz,2H),3.43(s,3H),3.73(s,3H),3.98(t,J=8.4Hz,2H),4.61(d,J=6.6Hz,2H),5.53(t,J=6.6Hz,1H),5.68(s,1H),5.86(s,1H),6.40(s,1H),6.93-6.95(m,2H),7.03-7.05(m,1H),7.23-7.27(m,2H),7.35-7.37(m,1H),7.45-7.50(m,1H),7 71(d,J=8.4Hz,1H),7.74(d,J=8.4Hz,2H)IR(KBr)3457,1480,1354,1244,1164,1099,978,817cm-1 |
I-1223 | mp199-201℃1H NMR(CDCl3)δ3.19(s,3H),3.72(s,3H),3.90(s,3H),4.20-4.27(m,4H),5.20(s,2H),6.53(s,1H),6.90-6.99(m,3H),7.25-7.65(m,9H)IR(KBr)3434,2938,1604,1586,1522,1484,1465,1432,1368,1339,1326,1249,1226,1203,1174,1146,1136,1106,1027cm-1 |
I-1224 | mp127-129℃1H NMR(CDCl3)δ1.57(s,3H),1.65(s,3H),1.76(s,3H),1.82(s,3H),3.46(s,3H),3.64(m,2H),3.76(s,3H),4.30(t,J=5.7Hz,1H),4.62(d,J=6.9Hz,2H),5.10(m,1H),5.53(m,1H),5.72(s,1H),5.85(s,1H),6.47(8,1H),6.93(dd,J=1.8,8.4Hz,1H),6.98(d,J=8.4Hz,1H),7.05(d,J=1.8Hz,1H),7.88(ABq,J=8.7Hz,4H)IR(KBr)3478,3314,2937,1585,1556,1518,1501,1484,1460,1417,1387,1363,1328,1279,1243,1228,1191,1155,1129,1113,1090,1068,1013cm-1 |
I-1225 | mp162-164℃1H NMR(CDCl3)δ3.19(s,3H),3.72(s,3H),4.19-4.23(m,4H),5.18(s,2H),6.52(s,1H),7.03-7.64(m,12H)IR(KBr)3433,2933,1523,1483,1463,1435,1377,1360,1269,1227,1172,1149,1126,1096cm-1 |
I-1226 | mp188-190℃1H NMR(DMSO)δ1.72(s,3H),1.75(s,3H),3.33(s,3H),3.67(s,3H),4.55(d,J=6.9Hz,2H),5.49(m,1H),6.50(s,1H),6.66(dd,J=2.1,8.1Hz,1H),6.74(d,J=2.1Hz,1H),6.91(d,J=8.1Hz,1H),7.42(bs,2H),7.85(ABq,J=8.4Hz,4H),8.75(bs,2H)IR(KBr)3465,2937,1588,1517,1500,1483,1470,1446,1415,1385,1340,1308,1283,1246,1224,1201,1186,1168,1130,1116,1091,1067,1011cm-1 |
I-1227 | mp172-174℃1H NMR(CDCl3)δ1.75(s,3H),1.78(s,H),3.19(s,3H),3.72(s,3H),3.87(s,3H),4.20-4.27(m,4H),4.62(d,J=6.9Hz,2H),5.57(m,1H),6.54(s,1H),6.96(s,3H),7.49(ABq,J=8.7Hz,4H)IR(KBr)3433,2937,1604,1582,1522,1483,1465,1432,1368,1340,1326,1242,1226,1218,1204,1174,1138,1107cm-1 |
I-1228 | mp169-175℃1H NMR(CDCl3)δ0.07-0.02(m,2H),0.34-0.42(m,2H),0.98(m,1H),2.44(s,3H),3.20(s,3H),3.47(d,J=7.2Hz,2H),3.78(s,3H),3.91(s,3H),5.22(s,2H),6.85(s,1H),6.91(dd,J=1.8,8.1Hz,1H),6.976(d,J=1.8Hz,1H),6.979(d,J=8.1Hz,1H),7.26-7.73(m,9H)IR(KBr)3447,2934,1604,1518,1480,1390,1362,1240,1227,1175,1140,1081cm-1 |
I-1229 | mp172-174℃1H NMR(CDCl3)δ1.74(s,3H),1.78(s,3H),3.71(s,3H),3.87(s,3H),4.20-4.25(m,4H),4.62(d,J=6.3Hz,2H),4.94(bs,1H),5.57(m,1H),6.55(s,1H),6.89-7.50(m,7H)IR(KBr)3410,2933,1611,1522,1484,1462,1422,1371,1264,1238,1224,1173,1134,1103cm-1 |
I-1230 | mp149-151℃1H NMR(CDCl3)δ1.75(s,3H),1.81(s,3H),3.45(s,3H),3.75(s,3H),3.87(s,3H),4.61(d,J=6.6Hz,2H),5.54-5.58(m,1H),5.69(s,1H),5.91(s,1H),6.46(s,1H),6.93-7.06(m,5H),7.58 (d,J=8.7Hz,2H)IR(KBr)3501,2939,1680,1609,1582,1520,1487,1458,1397,1284,1246,1191,1179,1115,1067,1015,940,822,794cm-1 |
I-1231 | mp151-152℃1H NMR(CDCl3)δ1.77(d,J=0.6Hz,3H),1.81(d,J=0.6Hz,3H),2.04(s,3H),2.08(s,3H),3.20(s,3H),3.77(brs,2H),3.86(s,3H),4.65(d,J=6.6Hz,2H),5.58(m,1H),6.04(s,1H),6.81(dd,J=2.1,8.7Hz,1H),6.81(d,J=2.1Hz,1H),7.01(d,J=8.7Hz,1H),7.30-7.36(m,2H),7.38-7.43(m,2H)IR(KBr)3484,3393,2934,1608,1511,1482,1371,1239,1213,1197,1173,1153,1138,989,973,871,844,791cm-1 |
I-1232 | mp198-199℃1H NMR(DMSO-d6)δ1.72(s,3H),1.77(s,3H),1.91(s,3H),1.95(s,3H),3.75(s,3H),4.04(s,2H),4.55(d,J=6.9Hz,2H),5.48(m,1H),6.40(s,1H),6.69(dd,J=1.8,8.1Hz,1H),6.75(d,J=1.8Hz,1H),6.77-6.83(m,2H),7.05-7.11(m,3H),9.39(s,1H)IR(KBr)3375,3287,2913,1609,1587,1578,1518,1484,1434,1403,1270,1235,1207,1171,1136,1032,1009,863,853,816,749cm-1 |
I-1233 | mp198-199℃1HNMR(CDCl3)δ1.77(s,3H),1.80(s,3H),1.91(s,3H),2.11(s,3H),2.13(s,3H),3.20(s,3H),3.84(s,3H),4.64(d,J=6.6Hz,2H),5.58(m,1H),6.46(s,1H),6.69-6.74(m,2H),6.96(d,J=8.4Hz,1H),7.11(s,1H),7.32-7.38(m,2H),7.40-7.46(m,2H)IR(KBr)1651,1513,1470,1448,1414,1368,1330,1267,1241,1214,1199,1175,970,869cm-1 |
I-1234 | mp193-194℃1H NMR(CDCl3)δ1.77(s,3H),1.80(d,J=0.6Hz,3H),1.94(s,3H),2.11(s,3H),2.13(s,3H),3.84(s,3H),4.64(d,J=6.6Hz,2H),5.58(m,1H),6.58(s,1H),6.70-6.75(m,2H),6.85-6.93(m,2H),6.96(d,J=8.4Hz,1H),7.13(s,1H),7.19-7.24(m,2H)IR(KBr) 3271,1654,1611,1517,1467,1448,1370,1289,1262,1240,1213,1177,1136,835cm-1 |
I-1235 | mp114-115℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.27(s,6H),3.91(s,3H),4.63(d,J=6.6Hz,2H),5.56(m,1H),5.61(s,1H),6.86(dd,J=2.1,8.4Hz,1H),6.86(d,J=2.1Hz,1H),6.97(H,J=8.4Hz,1H),7.02-7.14(m,5H)IR(KBr)3410,1597,1521,1470,1449,1415,1382,1297,1276,1261,1220,1122,1052,983,862cm-1 |
I-1236 | 粉末1H NMR(CDCl3)δ3.22(s,3H),3.38(s,3H),3.46(s,3H),3.92(s,3H),5.22(s,2H),5.76(s,1H),6.97-7.09(m,3H),7.32-7.51(m,9H)IR(KBr)3448,2935,1516,1455,1394,1366,1352,1246,1148,1076,1015,972,881,699,541,524cm-1 |
I-1237 | mp169-172℃1H NMR(CDCl3)δ2.49(s,3H),3.21(s,3H),3.47(s,3H),3.50(s,3H),3.92(s,3H),5.23(s,2H),6.95-7.04(m,3H),7.31-7.49(m,9H)IR(KBr)3009,2932,1518,1459,1370,1362,1250,1176,1151,872,809,542,527cm-1 |
I-1238 | mp182-184℃1H NMR(CDCl3)δ2.67(s,3H),3.21(s,3H),3.48(s,3H),3.50(s,3H),3.93(s,3H),5.77(s,1H),6.98-7.06(m,3H),7.38-7.51(m,4H)IR(KBr)3548,3502,2938,1602,1519,1389,1364,1176,1159,1012,963,875,521cm-1 |
I-1239 | mp132-135℃1H NMR(CDCl3)δ1.77(s,3H),1.80(s,3H),2.62(s,3H),3.21(s,3H),3.48(s,3H),3.51(s,3H),3.90(s,3H),4.64(d,J=6.6Hz,2H),5.51-5.58(m,1H),6.97-7.04(m,3H),7.37-7.51(m,4H)IR(KBr)2936,1518,1464,1375,1362,1246,1175,1153,1013,968,872,805,529cm-1 |
I-1240 | mp169-172℃1H NMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.38(s,3H),3.47(s,3H),3.89(s,3H),4.65(d,J=6.6Hz,2H),5.06(s,1H),5.54-5.61(m,1H),5.83(s,1H),6.92-7.00(m,3H),7.05-7.09(m,2H),7.28-7.33(m,2H)IR(KBr)3458,2935,1611,1520,1458,1392,1244,1222,1015,828,803cm-1 |
I-1241 | mp170-173℃1H NMR(CDCl3)δ1.73(s,3H),1.79(s,3H),2.55-3.00(m,3H),3.21(s,3H),3.22-3.80(m,6H),4.55-4.63(m,2H),5.41-5.47(m,1H),6.83(s,1H),7.03-7.70(m,8H)IR(KBr)2938,1686,1516,1481,1378,1235,1235,1179,1152,1081,847,799,675,527cm-1 |
I-1242 | mp117-118℃1H NMR(CDCl3)δ1.77(s,3H)1.81(d,J=0.6Hz,3H),2.11(s,3H),2.19(s,3H),3.38(s,3H),4.64(d,J=6.9Hz,2H),4.75(brs,1H),5.54-5.90(m,1H),6.86-0.91(m,2H),6.93(s,1H),7.10-7.69(m,3H),7.20-7.25(m,2H)IR(CHCl3)3596,3010,2934,1675,1519,1473,1262,1172,1098cm-1 |
I-1243 | 泡沫1H NMR(CDCl3)δ3.43(s,3H),3.72(s,3H),5.03(s,2H),6.43(s,1H),6.93(dd,J=8.4,2.1Hz,1H),6.94(d,J=8.7Hz,2H),7.09(d,J=2.1Hz,1H),7.11(d,J=8.4Hz,1H),7.29(ddd,J=7.8,4.8,1.5Hz,1H),7.49(brd,J=7.8Hz,1H),7.53(d,J=8.7Hz,2H),7.70(ddd,J=7.8,7.8,1.5Hz,1H),8.61(brd,J=4.8Hz,1H)IR(KBr)3432,1611,1588,1562,1523,1488,1467,1226,1114,1071,1015,939,824,778,758cm-1 |
I-1244 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.01(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.99(dd,J=8.4,2.1Hz,1H),7.10(d,J=2.1Hz,1H),7.14(d,J=8.4Hz,1H),7.30~7.36(m,3H),7.46~7.49(m,2H),7.54(d,J=8.7Hz,2H)IR(KBr)3433,1612,1589,1523,1489,1403,1224,1192,1113,1070,1013,938,813,758cm-1 |
I-1245 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.01(s,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.99(dd,J=5.1,3.6Hz,1H),6.99(dd,J=8.4,2.1Hz,1H),7.10(d,J=2.1Hz,1H),7.11(d,J=8.4Hz,1H),7.27(dd,J=3.6,1.0Hz,1H),7.29(dd,J=5.1,1.0Hz,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3433,1612,1589,1523,1488,1403,1241,1224,1192,1113,1070,1011,826cm-1 |
I-1246 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.93(s,2H),5.70(d,J=1.5Hz,1H),5.75(d,J=1.5Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.99(dd,J=8.4,2.1Hz,1H),7.05(d,J=8.4Hz,1H),7.10(d,J=2.1Hz,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3432,1611,1590,1523,1489,1403,1224,1193,1113,1071,1010,938,826cm-1 |
I-1247 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),5.53(d,J=10.5Hz,1H),5.69(d,J=16.5Hz,1H),6.11(ddd,J=16.5,10.5,6.3Hz,1H),6.44(d,J=6.3Hz,1H),6.45(s,1H),6.88(d,J=8.4Hz,1H),6.91~6.93(m,2H),6.92(d,J=8.7Hz,2H),7.53(d,J=8.7Hz,2H)IR(KBr)3433,1611,1592,1522,1485,1403,1226,1106,1059,814cm-1 |
I-1248 | 泡沫1H NMR(CDCl3)δ1.16(t,J=7.5Hz,3H),2.26(tq,J=2.1,7.5Hz,2H),3.45(s,3H),3.75(s,3H),4.76(t,,J=2.1Hz,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.96(dd,J=2.1,8.4Hz,1H),7.06(d,J=8.4Hz,1H),7.07(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3434,2230,1612,1590,1523,1479,1225,1113,1070,1005,938,815cm-1 |
I-1249 | 泡沫1H NMR(CDCl3)δ3.38(s,3H),3.67(s,3H),5.12(s,2H), 6.43(s,1H),6.56(d,J=3.3Hz,1H),6.79(dd,J=2.1,8.1Hz,1H),6.84(d,J=8.7Hz,2H),6.87(d,J=2.1Hz,1H),7.02(d,J=3.3Hz,1H),7.02(d,J=8.1Hz,1H),7.45(d,J=8.7Hz,2H)IR(KBr)3431,1698,1611,1523,1489,1405,1246,1114,1071,1012,816,786cm-1 |
I-1250 | 1H NMR(CDCl3)δ3.38(s,3H),3.67(s,3H),4.66(tt,J=2.7,6.9Hz,2H),4.90(tt,J=2.7,6.9Hz,2H),5.43(tt,J=6.9,6.9Hz,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.96(br.s,2H),7.07(s,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3430,1955,1612,1589,1522,1489,1404,1248,1113,1070,1008,938,845,825cm-1 |
I-1251 | 泡沫1H NMR(CDCl3)δ1.69(dd,J=3.3,6.9Hz,3H),3.46(s,3H),3.74(s,3H),4.63(dd,J=2.4,6.3Hz,2H),5.28(m,1H),5.33(m,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.95(d,J=1.5Hz,1H),6.96(br.s,1H),7.06(d,J=1.5Hz,1H),7.52(d,J=8.7Hz,2H)IR(KBr)3436,2933,1968,1612,1587,1523,1489,1464,1404,1112,1071,1011,998,824cm-1 |
I-1252 | 泡沫1H NMR(CDCl3)δ1.02(t,J=7.2Hz,3H),2.05(ddq,J=3.3,6.3,7.2Hz,2H),3.46(s,3H),3.74(s,3H),4.64(dd,J=2.4,6.0Hz,2H),5.40(m,2H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.94(d,J=2.1,8.4Hz,1H),6.97(d,J=8.4Hz,1H),7.06(d,J=2.1Hz,1H),7.54(d,J=8.7Hz,2H)IR(KBr)3479,2960,2933,1964,1612,1582,1522,1489,1403,1242,1113,1072,1011,999,944,872cm-1 |
I-1253 | 泡沫1H NMR(CDCl3)δ1.03(d,J=6.6Hz,6H),2.34(m,1H),3.46(s,3H),3.74(s,3H),4.63(dd,J=2.7,6.3Hz,2H),5.33(m,1H),5.44(m,1H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.93(d,J=1.8,7.8Hz,1H),6.97(d,J=7.8Hz,1H),7.06(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3434,2958,1960,1612,1589,1523,1489,1226,1113,1071,1011,939,825cm-1 |
I-1254 | 泡沫1H NMR(CDCl3)δ2.62(d,J=2.4Hz,1H),3.45(s,3H),3.75(s,3H),4.18(dd,J=7.2,11.4Hz,1H),4.38(dd,J=2.4,11.4Hz,1H),4.94(ddd,J=2.4,2.4,7.2Hz,1H),6.44(s,1H),6.92(d,J=8.7Hz,2H),6.98(d,J=8.4Hz,1H),7.01(d,J=1.8,8.4Hz,1H),7.08(d,J=1.8Hz,1H),7.52(d,J=8.7Hz,2H)IR(KBr)3434,3283,2127,1612,1586,15323,1487,1226,1115,1069,1007,943,825cm-1 |
I-1255 | mp148-150℃1H NMR(CDCl3)δ2.99(s,6H),3.75-3.80(br,2H),3.75(s,3H),3.77(s,3H),6.45-6.53(m,2H),6.79-6.83(m,2H),6.88(s,1H),6.95(s,1H),7.17-7.23(m,1H),7.48-7.51(m,2H)IR(KBr)3600-2800(br),1630,1609,1530,1492,1461,1444,1388,1331,1209,1165,1125,1050,1028cm-1 |
I-1256 | mp209-212℃1H NMR(CDCl3)δ3.00(s,6H),3.11(s,3H),3.76(s,3H),3.79(s,3H),6.66(brs,1H),6.78-6.83(m,2H),6.87(s,1H),6.98(s,1H),7.02(dd,J=2.4,8.4Hz,1H),7.10(dd,J=2.4,10.8Hz,1H),7.39-7.52(m,3H)IR(KBr)3600-2800(br),1627,1609,1530,1494,1463,1390,1325,1213,1154,1127,1052,1028,984cm-1 |
I-1257 | mp198-200℃1H NMR(CDCl3)δ1.43(t,J=7.5Hz,3H),3.00(s,3H),3.19-3.26(m,2H),3.76(s,3H),3.79(s,3H),6.69(brs,1H),6.79-6.85(m,2H),6.86(s,1H),6.97(s,1H),7.01(dd,J=2.4,8.4Hz,1H),7.09(dd,J=2.4,10.8Hz,1H),7.37-7.53(m,3H)IR(KBr)3600-2800(br),1611,1530,1492,1495,1445,1389,1355,1325,1207,1163,1141,1122,1051,1025,981cm-1 |
I-1258 | IR(KBr)1612,1526,1490,1444,1349,1301,1196,1129,1038cm-1mp102-103℃1H NMR(CDCl3)δ2.27(s,3H),2.31(s,3H),3.00(s,6H),4.78(d,J=6.6Hz,2H),6.24(t,J=6.6Hz,1H),6.80(d,J=8.4Hz,2H),6.96-7.16(m,5H),7.26(d,J=8.4Hz,2H) |
I-1259 | mp114-115℃1H NMR(CDCl3)δ1.75(s,3H),1.79(s,3H),3.61(s,3H),3.65(s,3H),3.74(s,3H),3.87(s,3H),3.88(s,3H),4.63(d,J=6.9Hz,2H),5.54-5.62(m,1H),6.68(s,1H),6.94-7.03(m,5H),7.54(d,J=9.0Hz,2H)IR(KBr)3433,2932,1682,1605,1580,1519,1465,1439,1389,1290,1253,1237,1186,1140,1109,1089,1039,1029,992,833cm-1 |
I-1260 | mp163-165℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.19(s,3H),3.72(s,3H),4.20-4.26(m,4H),4.62(d,J=6.6Hz,2H),5.55(m,1H),6.53(s,1H),7.00-7.20(m,3H),7.49(ABq,J=8.1Hz,4H)IR(KBr)3433,2933,1523,1483,1463,1433,1371,1359,1340,1299,1266,1227,1220,1172,1149,1127,1098cm-1 |
I-1261 | mp135-137℃1H NMR(CDCl3)δ-0.03-0.03(m,2H),0.36-0.42(m,2H),1.00(m,1H),1.75(s,3H),1.79(s,3H),2.56(s,3H),3.20(s,3H),3.48(d,J=4.8Hz,2H),3.78(s,3H),3.88(s,3H),4.63(d,J=6.9Hz,2H),5.54(m,1H),6.86(s,1H),6.95-6.97(m,3H),7.55(ABq,J=8.7Hz,4H)IR(KBr)3433,2936,1604,1519,1481,1467,1369,1336,1245,1231,1201,1177,1153,1081cm-1 |
I-1262 | mp181-182℃1H NMR(CDCl3)δ1.76(s,3H),1.80(s,3H),3.72(s,3H),4.19-4.26(m,4H),4.62(d,J=6.9Hz,2H),4.91(bs,1H),5.55(m,1H),6.53(s,1H),6.89-7.49(m,7H)IR(KBr)3404,1612,1523,1485,1462,1434,1373,1266,1227,1212,1116,1101cm-1 |
I-1263 | mp80-82℃1H NMR(CDCl3)δ-0.05-0.09(m,2H),0.44-0.51(m,2H),1.04(m,1H),1.74(s,3H),1.78(s,3H),3.33(d,J=4.8Hz,2H),3.75(s,3H),3.88(s,3H),4.63(d,J=6.6Hz,2H),4.98(s,1H),5.57(m,1H),6.15(s,1H),6.46(s,1H),6.89-7.03(m,5H),7.52-7.56(m,2H)IR(KBr)3374,1614,1523,1490,1465,1446,1391,1267,1235,1172,1113,1073cm-1 |
I-1264 | mp112-113℃1H NMR(CDCl3)δ2.19(s,3H),2.28(s,3H),3.91(s,3H),5.20(s,2H),6.84-6.86(m,1H),6.92-6.97(m,2H),7.09(s,1H),7.16(s,1H),7.31-7.43(m,5H),7.47-7.49(m,2H),7.60(d,J=10.2Hz,1H),8.01(brs,1H)IR(KBr)3421,3303,2935,1711,1519,1490,1365,1231,1198,1178,1134,1009,864cm-1 |
I-1265 | mp85-86℃1H NMR(ClCl3)δ2.85(s,3H),3.32(s,3H),3.82(s,3H),3.96(s,3H),5.38(s,2H),7.04(s,1H),7.22(s,1H),7.25(d,J=8.4Hz,1H),7.35(d,J=8.4Hz,1H),7.48-7.67(m,7H),8.45(brs,1H)IR(KBr)3432,2938,1740,1608,1517,1483,1396,1366,1271,1179,1111,1080,832,810,698cm-1 |
I-1266 | mp79-80℃1H NMR(CDCl3)δ2.14(s,3H),3.50(s,3H),4.95(brs,1H),5.22(s,2H),5.88(brs,1H),6.81(s,1H),6.94(d,J=8.1Hz,2H),7.02-7.14(m,3H),7.37-7.56(m,7H)IR(KBr)3409,2933,1612,1522,1488,1454,1400,1266,1229,1199,1162,1007,834,696cm-1 |
I-1267 | mp87-88℃1H NMR(CDCl3)δ2.13(s,3H),2.59(s,3H),3.20(s,3H),3.55(s,3H),5.22(s,2H),6.99-7.17(m,5H),7.34-7.48(m,6H),7.67(d,J=8.4Hz,2H)IR(KBr)3428,2931,1612,1522,1488,1454,1400,1266,1230,1163,1007,835cm-1 |
I-1268 | mp76-77℃1H NMR(CDCl3)δ1.72(s,3H),1.77(s,6H),1.81(s,3H),2.69(s,3H),3.24(s,3H),3.61(s,3H),3.79(s,3H),4.12-4.20(m,1H),4.55-4.61(m,1H),4.64(d,J=6.6Hz,2H),5.25(t,J=7.5Hz,1H),5.50(t,J=6.4Hz,1H),6.85(s,1H),7.05-7.11(m,2H),7.34-7.40(m,3H)IR(KBr)3423,2939,1707,1521,1484,1367,1241,1178,1079,1034,972,799,521cm-1 |
I-1269 | mp73-74℃1H NMR(CDCl3)δ2.17(s,3H),2.28(s,3H),5.16(s,2H),5.71(brs,1H),6.83(d,J=8.1Hz,1H),6.97-7.00(m,2H),7.08(s,1H),7.15(s,1H),7.32-7.33(m,2H),7.36-7.45(m,5H),7.60(d,J=10.5Hz,1H),8.05(brs,1H)IR(KBr)3410,2923,1718,1606,1540,1521,1489,1424,1282,1179,976,728cm-1 |
I-1270 | mp65-67℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.14(s,3H),2.72(s,3H),3.20(s,3H),3.56(s,3H),4.64(d,J=6.9Hz,2H),5.53(t,J=6.6Hz,1H),7.01-7.11(m,3H),7.18(s,1H),7.37(d,J=8.7Hz,2H),7.67(d,J=8.7Hz,2H),IR(KBr)3434,2938,1519,1478,1365,1267,1176,1151,968,871,799,524cm-1 |
I-1271 | mp99-100℃1H NMR(CDCl3)δ1.76(s,6H),1.79(s,3H),1.81(s,3H),3.52(s,3H),3.72(s,3H),4.61(d,J=7.2Hz,2H),5.36(t,J=6.6Hz,1H),5.53(t,J=5.7Hz,1H),5.69(brs,1H),5.81(brs,1H),6.43(s,1H),6.46-6.52(m,1H),6.95(s,2H),7.05(s,1H),7.10-7.16(m,1H)IR(KBr)3496,3407,2933,1638,1535,1493,1098,1000cm-1 |
I-1272 | mp75-76℃1H NMR(CDCl3)δ2.17(s,3H),2.28(s,3H),3.12(s,3H),5.18(s,2H),7.09-7.14(m,4H),7.26-7.47(m,8H),7.61(d,J=11.4Hz,1H),8.00(brs,1H)IR(KBr)3330,2927,1731,1607,1541,1521,1488,1364,1290,1169,1105,975,878,811cm-1 |
I-1273 | mp112-113℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.11(s,3H),3.47(s,3H),4.64(d,J=6.6Hz,2H),4.83(brs,1H),5.56(t,J=7.2Hz,1H),5.84(brs,1H),6.78(s,1H),6.91(d,J=8.7Hz,2H),7.02-7.10(m,3H),7.51(d,J=8.4Hz,2H),IR(KBr)3498,2978,1613,1522,1487,1453,1302,1204,1232,1196,987,812cm-1 |
I-1274 | 油状物1H NMR(CDCl3)δ1.73(s,3H),1.76(s,3H),1.77(s,3H),1.79(s,3H),2.22(s,3H),2.27(s,3H),3.73(d,J=6.0Hz,2H),3.88(s,3H),4.63(d,J=6.6Hz,2H),5.36(t,J=6.0Hz,1H),5.57(t,J=6.6Hz,1H),6.40-6.51(m,2H),6.87-6.95(m,3H),7.05-7.14(m,3H)IR(CHCl3)3021,2934,1628,1523,1492,1235,1219,1139cm-1 |
I-1275 | mp64-65℃1H NMR(CDCl3)δ1.74(s,3H),1.77(s,6H),1.82(s,3H),2.16(s,3H),2.29(s,3H),3.23(s,3H),4.36(d,J=7.5Hz,2H),4.64(d,J=6.3Hz,2H),5.28(t,J=8.4Hz,1H),5.51(t,J=6.3Hz,1H),7.01-7.16(m,6H),7.24-7.35(m,2H)IR(KBr)3422,2926,1698,1519,1489,1367,1209,1170,962,807cm-1 |
I-1276 | 油状物1H NMR(CDCl3)δ2.21(s,3H),2.26(s,3H),3.95(d,J=6.6Hz,2H),4.28(brs,1H),478(d,J=6.0Hz,2H),6.05(t,J=6.3Hz,1H),6.24(t,J=6.3Hz,1H),6.36-6.49(m,2H),6.97-7.15(m,6H)IR(CHCl3)3446,3009,1628,1525,1492,1274,1224,1130,883cm-1 |
I-1277 | mp64-65℃1H NMR(CDCl3)δ1.76(s,3H),1.80(s,6H),1.85(s,3H),2.23(s,3H),2.30(s,3H),3.74(d,J=6.3Hz,2H),4.64(d,J=6.0Hz,2H),5.38(t,J=6.6Hz,1H),5.55(t,J=6.9Hz,1H),5.73(brs,1H),6.41-6.50(m,2H),6.84-7.15(m,6H)IR(KBr)3354,2971,1627,1522,1490,1274,1200,1128,990,843cm-1 |
I-1278 | mp153-154℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),1.95(s,12H),4.64(d,J=6.9Hz,2H),4.78(s,1H),5.57(t,J=6.9Hz,1H),6.85(ddd,J=8.3,2.1,1.2Hz,1H),6.90(d,J=8.6Hz,2H),6.92(dd,J=12.0,2.1Hz,1H),7.04(d,J=8.6Hz,2H),7.04(t,J=8.3Hz,1H),IR(KBr)3433,1514,1293,1262,1242,1112,984cm-1 |
I-1279 | mp115-117℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),2.23(s,3H),3.21(s,3H),3.81(s,3H),4.63(d,J=6.6Hz,2H),5.55(t,J=6.6Hz,1H),6.81(s,1H),7.02(t,J=8.6Hz,1H),7.20(s,1H),7.24-7.28(m,1H),7.33-7.44(m,3H)IR(KBr)3434,1522,1492,1337,1218,1200,1148,979,876cm-1 |
I-1280 | mp88-90℃1H NMR(CDCl3)δ1.76(s,3H),1.80(s,3H),2.24(s,3H),3.80(s,3H),4.63(d,J=6.7Hz,2H),4.88(brs,1H),5.55(t,J=6.7Hz,1H),6.83(s,1H),6.90(d,J=8.7Hz,2H),7.01(t,J=8.6Hz,1H),7.18(s,1H),7.24-7.28(m,3H),7.36(dd,J=12.9,2.1Hz,1H)IR(KBr)3400,1523,1493,1263,1217,1128,977,836cm-1 |
I-1281 | mp158-159℃1H NMR(CDCl3)δ1.76(s,3H),1.80(d,J=0.3Hz,3H),2.10(s,3H),2.34(s,3H),2.50(s,3H),3.87(s,3H),4.63(d,J=6.9Hz,2H),5.14(s,1H),5.55(m,1H),5.88(s,1H),6.77-6.82(m,2H),6.85-6.91(m,2H),6.98(d,J=8.1Hz,1H),7.13(s,1H),7.18-7.24(m,2H)IR(KBr)3465,1610,1516,1473,1382,1322,1307,1266,1240,1213,1179,1168,1147,1100,982,836cm-1 |
I-1282 | mp85-86℃1H NMR(CDCl3)δ0.99(d,J=6.2Hz,6H),1.71-1.98(m,3H),2.27(s,3H),2.29(s,3H),3.20(s,3H),3,88(s,3H),4.10(t,J=6.8Hz,2H),6.88(dd,J=2.0,8.6Hz,1H),6.88(d,J=2.0Hz,1H),6.95(d,J=8.6Hz,1H),7.30-7.46(m,4H)IR(KBr)1519,1488,1375,1255,1243,1214,1204,1173,154,1134,867,850,792cm-1 |
I-1283 | mp117-118℃1H NMR(CDCl3)δ0.99(d,J=6.3Hz,6H),1.75-1.94(m,3H),2.27(s,3H),2.28(s,3H),3.88(s,3H),4.10(t,J=6.6Hz,2H),4.91(s,1H),6.86-6.91(m,4H),6.94(d,J=8.7Hz,1H),7.12(s,1H),7.15(s,1H),7.22-7.27(m,2H)IR(KBr)3438,1611,1522,1490,1475,1464,1446,1256,1242,1212,1180,1171,1137,1032,834,818cm-1 |
I-1284 | mp156-157℃1H NMR(CDCl3)δ3.46(s,3H),3.76(s,3H),3.89(s,3H),4.78(J,J=6.3Hz,2H),4.99(s,1H),5.96(s,1H),6.25(t,J=6.3Hz,1H),6.47(s,1H),6.90-6.95(m,2H),6.93(d,J=7.8Hz,1H),7.04(dd,J=2.1,7.8Hz,1H),7.04(d,J=2.1Hz,1H),7.51-7.57(m,2H)IR(KBr)3455,1612,1522,1487,1456,1396,1269,1234,1223,1209,1173,1140,1115,1024,885,825,813cm-1 |
I-1285 | mp84-85℃1H NMR(CDCl3)δ1.00(d,J=6.6Hz,6H),1.71-1.96(m,3H),2.27(s,6H),4.11(t,J=6.9Hz,2H),4.80(brs,1H),6.86-6.92(m,2H),6.97-7.14(m,5H),7.22-7.27(m,2H)IR(KBr)3389,1523,1491,1476,1427,1301,1276,1233,1196,1168,1126,836,815cm-1 |
I-1286 | mp152-153℃1H NMR(CDCl3)δ1.76(s,3H),1.80(d,J=0.6Hz,3H),2.12(s,3H),2.20(s,3H),3.39(s,3H),3.87(s,3H),4.64(d,J=6.3Hz,2H),4.79(brs,1H),5.56-5.61(m,1H),6.82-6.97(m,6H),7.21-7.26(m,2H)IR(CHCl3)3596,3440,3011,2935,1676,1612,1588,1518,1473,1449,1259,1238,1173cm-1 |
I-1287 | mp123-125℃1H NMR(CDCl3)δ-0.01-0.08(m,2H),0.44-0.50(m,2H),1.01(m,1H),3.21(s,3H),3.34(d,J=7.5Hz,2H),3.75(s,3H),3.91(s,3H),5.21(s,2H),6.08(s,1H),6.45(s,1H),6.97-7.04(m,3H),7.26-7.72(m,9H) |
I-1288 | mp177-178℃1H NMR(CDCl3)δ0.27(t,J=4.8Hz,1H),0.60(dd,J=4.8,8.7Hz,1H),1.13(s,3H),1.17(s,3H),1.13-1.22(m,1H),3.46(s,3H),3.75(s,3H),3.80(s,3H),4.00(dd,J=7.8,10.5Hz,1H),4 12(dd,J=6.6,10.5Hz,1H),4.95(bs,1H),5.91(s,1H),6.46(s,1H),6.91-7.02(m,5H),7.52-7.56(m,2H)IR(KBr)3479,3434,3389,2940,1614,1589,1523,1490,1466,1395,1361,1319,1271,1238,1218,1174,1137,1117,1072,1011cm-1 |
I-1289 | mp153-155℃1H NMR(CDCl3)δ1.76(s,3H),1.80(s,3H),2.25(s,3H),3.80(s,3H),3.89(s,3H),4.63-4.65(d,J=6.6Hz,2H),4.80(br,1H),5.57(m,1H),6.86-6.97(m,6H),7.18(s,1H),7.45-7.48(m,2H)IR(CHCl3)3596,1609,1523,1493,1464,1387,1256,1173,1138,1042,1032,997,834cm-1 |
I-1290 | mp150-152℃1H NMR(CDCl3)δ2.25(s,3H),3.80(s,3H),3.90(s,3H),4.74-4.80(m,3H),6.26(t,J=6.0Hz,1H),6.85-6.92(m,6H),7.19(s,1H),7.45-7.48(m,2H)IR(CHCl3)3596,2958,2938,1609,1523,1493,1464,1389,1328,1257,1173,1140,1102,1030,886,854,834cm-1 |
I-1291 | mp117-118℃1H NMR(CDCl3)δ1.76(s,3H),1.79(s,3H),2.28(s,3H),2.31(s,3H),3.01(s,6H),3.88(s,3H),4.63(d,J=6.6Hz,2H),5.53-5.60(m,1H),6.76-6.96(m,5H),7.15(s,2H),7.28(d,J=8.7Hz,2H)IR(KBr)1611,1529,1490,1447,1359,1322,1239,1214,1193,1135,1038,cm-1 |
I-1292 | mp116-118℃1H NMR(CDCl3)2.24(s,3H),3.81(s,3H),4.77(d,J=6.3Hz,2H),4.90(brs,1H),6.23(t,J=6.3Hz,1H),6.83(s,1H),6.90(d,J=8.7Hz,2H),6.99(t,J=8.6Hz,1H),7.17(s,1H),7.25(d,J=8.7Hz,2H),7.27(ddd,J=8.6,2.1,1.2Hz,1H),7.37(dd,J=12.6,2.1Hz,1H)IR(KBr)3596,1731,1613,1523,1493,1259,1130,1033,885cm-1 |
I-1293 | mp151-154℃1H NMR(CDCl3)δ2.23(s,3H),3.21(s,3H),3.80(s,3H),3.93(s,3H),5.20(s,2H),6.81(s,1H),6.95(d,J=8.4Hz,1H),7.05(dd,J=8.4,2.1Hz,1H),7.15(d,J=2.1Hz,1H),7.21(s,1H),7.30-7.50(m,9H)IR(KBr)1490,1361,1243,1148,1032,876cm-1 |
I-1294 | mp119-121℃1H NMR(CDCl3)δ1.76(s,3H),1.79(s,3H),2.24(s,3H),3.21(s,3H),3.80(s,3H),3.91(s,3H),4.63(d,J=6.5Hz,2H),5.56(t,J=6.5Hz,1H),6.82(s,1H),6.94(d,J=8.4Hz,1H),7.10(dd,J=8.4,1.5Hz,1H),7.13(d,J=1.5Hz,1H),7.23(s,1H),7.36(d,J=8.3Hz,2H),7.43(d,J=8.3Hz,2H)IR(KBr)1519,1490,1364,1156,1031,971,858cm-1 |
I-1295 | mp135-137℃1H NMR(CDCl3)δ1.75(s,3H),1.78(s,3H),2.25(s,3H),3.80(s,3H),3.90(s,3H),4.63(d,J=6.7Hz,2H),4.95(s,1H),5.56(t,J=6.7Hz,1H),6.84(s,1H),6.90(d,J=8.7Hz,2H),6.94(d,J=8.3Hz,1H),7.10(1d,J=8.3,2.1Hz,1H),7.13(d,J=2.1Hz,1H),7.21(s,1H),7.26(d,J=8.7Hz,2H)IR(KBr)3423,1609,1523,1493,1258,1219,1142,1033,834cm-1 |
I-1296 | mp140-141℃1H NMR(CDCl3)δ1.46(t,J=6.9Hz,3H),3.46(s,3H),3.75(s,3H),4.13(q,J=6.9Hz,2H),4.77(d,J=6.0Hz,2H),5.05(s,1H),5.95(s,1H),6.25(t,J=6.0Hz,1H),6.47(s,1H),6.90-6.97(m,3H),7.01-7.06(m,2H),7.50-7.57(m,2H)IR(KBr)3463,3433,1613,1521,1491,1259,1400,1267,1235,1204,1167,1136,1112,1097,1076,1019,993,882,824,811cm-1 |
I-1297 | mp204-205℃1H NMR(DMSO-d6)δ2.21(s,3H),2.22(s,3H),2.87(s,3H),3.02(s,3H),4.96(s,2H),6.80-6.86(m,2H),7.05-7.11(m,4H),7.13-7.19(m,2H),7.20-7.27(m,1H)IR(KBr)3153,1644,1590,1522,1487,1437,1314,1264,1231,1197,1127,1067,833cm-1 |
I-1298 | mp155-158℃1H NMR(CDCl3)δ3.21(s,3H),3.45(s,3H),3.75(s,3H),4.42(s,4H),5.93(s,1H),6.44(s,1H),6.90-6.96(m,1H),7.06-7.11(m,1H),7.19-7.39(m,13H),7.67-7.72(m,2H)IR(KBr)3445,2940,1615,1521,1483,1367,1149,875,707,546,526cm-1 |
I-1299 | mp174-175℃1H NMR(CDCl3)δ2.15(s,3H),3.20(s,3H),3.53(s,3H),3.78(s,3H),4.40(s,4H),6.82(s,1H),6.91-7.01(m,2H),7.11-7.39(m,13H),7.65-7.70(m,2H)IR(KBr)3028,2936,1618,15200,1482,1365,1176,1151,1079,871,798,698,527cm-1 |
I-1300 | mp218-221℃1H NMR(CDCl3)δ2.69(s,3H),3.21(s,3H),3.55(s,3H),3.77(s,3H),6.83(s,1H),6.86-6.93(m,1H),7.02-7.15(m,2H),7.35-7.41(m,2H),7.66-7.71(m,2H)IR(KBr)3435,3389,2940,1635,1525,1362,1175,1152,1076,962,874,802,527cm-1 |
I-1301 | mp209-211℃1H NMR(CDCl3)δ2.91(s,3H),3.22(s,3H),3.54(s,3H),3.78(s,3H),6.86(s,1H),7.26-7.33(m,2H),7.37-7.42(m,2H),7.64-7.71(m,2H),8.15(s,1H),8.34-8.41(m,1H)IR(KBr)3336,2943,1736,1539,1480,1356,1174,1151,1077,881,799,523,507cm-1 |
I-1302 | 粉末1H NMR(CDCl3)δ1.50(s,3H),1.71(s,3H),2.78(s,3H),3.23(s,3H),3.55(s,3H),3.78(s,3H),4.11-4.20(m,1H),4.54-4.63(m,1H),5.20-5.28(m,1H),6.87(s,1H),7.25-7.31(m,3H),7.37-7.42(m,2H),7.66-7.72(m,2H)IR(KBr)2941,1702,1482,1369,1203,1176,1152,1080,964,873,797,525cm-1 |
I-1303 | mp133-136℃1H NMR(CDCl3)δ1.73(s,3H),1.77(s,3H),3.45(s,3H),3.74-3.78(m,5H),4.96(s,1H),5.34-5.42(m,1H),5.94(s,1H),6.45(s,1H),6.75-6.81(m,1H),6.89-6.95(m,2H),7.10-7.18(m,2H),7.51-7.56(m,2H)IR(KBr)3401,2935,1626,1614,1527,1490,1402,1267,1223,1113,1071,1005,829,589cm-1 |
I-1304 | mp170-171℃1H NMR(CDCl3)δ2.11(s,3H),3.47(s,3H),4.40(s,4H),4.91(s,1H),5.81(s,1H),6.77(s,1H),6.86-7.08(m,5H),7.22-7.33(m,10H),7.48-7.53(m,2H)IR(KBr)3483,3029,1612,1523,1489,1453,1400,1265,1215,834,749,698,494,526cm-1 |
I-1305 | mp166-168℃1H NMR(CDCl3)δ2.15(s,3H),2.17(s,3H),3.19(s,3H),4.21-4.59(m,4H),6.84-7.05(m,3H),7.14-7.15(m,1H),7.20-7.38(m,12H),7.63-7.69(m,2H)IR(KBr)3028,2938,1519,1476,1454,1363,1174,1151,969,873,801,700,525cm-1 |
I-1306 | mp210-212℃1H NMR(CDCl3)δ2.11(s,3H),2.90(s,3H),3.44(s,3H),3.52(s,3H),6.82-7.02(m,3H),7.30(s,1H),7.44-7.49(m,2H),7.65-7.71(m,2H)IR(KBr)3401,2850,1632,1478,1365,1177,1151,967,877,800,526cm-1 |
I-1307 | mp171-173℃1H NMR(CDCl3)δ2.13(s,3H),2.95(s,3H),3.22(s,3H),3.55(s,3H),7.17-7.22(m,3H),7.35-7.41(m,2H),7.64-7.69(m,2H),8.17(s,1H),8.37-8.43(m,1H)IR(KBr)3431,3034,2942,1741,1538,1478,1364,1291,1152,971,870,801,525cm-1 |
I-1308 | 粉末1H NMR(CDCl3)δ1.47(s,3H),1.70(s,3H),2.11(s,3H),2.67-3.15(m,3H),3.22(s,3H),3.56(s,3H),4.13-4.22(m,1H),4.54-4.63(m,1H),5.21-5.28(m,1H),7.09-7.42(m,6H),7.63-7.71(m,2H)IR(CHCl3)2940,1700,1519,1478,1372,1175,1151,968cm-1 |
I-1309 | mp139-141℃1H NMR(CDCl3)δ1.74(s,3H),1.78(s,3H),2.13(s,3H),3.48(s,3H),3.77(d,J=6.6Hz,2H),4.70-5.20(brs,1H),5.35-5.42(m,1H),5.77(s,1H),6.77-6.83(m,2H),6.88-6.99(m,4H),7.48-7.54(m,2H)IR(KBr)3525,3377,2931,1625,1526,1488,1222,1164,1011,833cm-1 |
I-1310 | mp177-179℃1H NMR(CDCl3)δ1.76(s,3H),1.81(s,3H),3.20(t,J=8.4Hz,2H),3.21(t,J=8.4Hz,2H),4.521(d,J=7.2Hz,2H),4.523(t,J=8.4Hz,2H),4.90(brs,1H),5.53(t,J=6.8Hz,1H),6.71(s,1H),6.89(d,J=8.4Hz,2H),6.98(d,J=8.7Hz,2H),7.41(d,J=8.7Hz,2H),7.45(d,J=9.0Hz,2H)IR(KBr)3389,2971,2911,1811,1525,1394,1238,1175,997,828cm-1 |
I-1311 | mp175-177℃1H NMR(CDCl3)δ3.20(t,J=8.3Hz,4H),4.53(t,J=8.4Hz,4H),4.70(d,J=6.3Hz,2H),4.88(brs,1H),6.19(t,J=6.2Hz,1H),6.89(d,J=8.7Hz,2H),6.96(d,J=9.0Hz,2H),7.41(d,J=9.0Hz,2H),7.47(d,J=8.7Hz,2H)IR(KBr)3409,3269,2934,2901,1524,1480,1395,1235,1223,1003,881,817cm-1 |
I-1312 | mp186-187℃1H NMR(CDCl3)δ2.06(s,3H),2.16(s,3H),4.72(s,1H),4.80(d,J=6.3Hz,2H),4.83(s,1H),6.25(t,J=6.3Hz,1H),6.76(s,1H),6.86-6.92(m,2H),7.03-7.13(m,3H),7.21-7.26(m,2H)IR(CHCl3)3689,3598,3551,3024,3008,1732,1614,1520,1487,1260,1223cm-1 |
I-1313 | mp201℃1H NMR(CDCl3)δ2.08(s,3H),2.17(s,3H),3.88(s,3H),4.80(d,J=6.3Hz,2H),4.90(brs,1H),4.99(s,1H),6.26(t,J=6.3Hz,1H),6.77(s,1H),6.85-6.92(m,4H),7.01(d,J=6.9Hz,1H),7.22-7.27(m,2H)IR(CHCl3)3688,3598,3538,3024,3014,2938,1731,1631,1520,1488,1240,1172cm-1 |
I-1314 | mp132-134℃1H NMR(CDCl3)δ2.12(s,3H),2.29(s,3H),3.00(s,6H),3.74(br,2H),6.62(dd,J=2.4,8.1Hz,1H),6.77-6.82(m,3H),7.01-7.05(m,2H),7.12(s,1H),7.26-7.31(m,2H)IR(KBr)3600-2800(br),1610,1523,1483,1443,1325,1297cm-1 |
I-1315 | mp123-125℃1H NMR(CDCl3)δ2.13(s,3H),2.29(m,4H),3.00(s,6H),3.98(br,3H),6.63(dd,J=2.4,8.1Hz,1H),6.77-6.81(m,3H),7.02(s,1H),7.09-7.13(m,2H),7.25-7.32(m,2H)IR(KBr)3600-2800(br),1609,1525,1488,1443,1356,1232,1194cm-1 |
I-1316 | mp125-127℃1H NMR(CDCl3)δ2.10(s,3H),2.31(s,3H),3.01(s,6H),6.77-6.84(m,2H),7.00(s,1H),7.15(s,1H),7.27-7.33(m,3H),7.52(dd,J=3.0,12.9Hz,1H),7.09(d,J=3.0Hz,1H),7.95(brs,1H)IR(KBr)3600-2800(br),1707,1611,1528,1484,1350,1279,1229,1196,1154cm-1 |
I-1317 | mp94-95℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.26(s,6H),4.63(d,J=6.6Hz,2H),5.51-5.60(m,1H),6.01(s,2H),6.78-6.89(m,3H),6.97-7.15(m,5H) |
I-1318 | 1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.29(s,6H),4.64(d,J=6.3Hz,2H),5.53-5.60(m,1H),6.99-7.21(m,5H),7.33-7.39(m,2H),7.49(d.d,J=5.4&0.3Hz,1H),7.80(s,1H),7.92(d,J=8.1Hz,1H) |
I-1319 | mp188-189℃1H NMR(CDCl3)δ1.31(t,J=7.5Hz,3H),2.26(s,3H),2.29(s,3H),2.68(q,J=7.5Hz,2H),5.17(s,2H),5.70(brs,1H),6.83(d,J=6.8Hz,1H),6.98-7.00(m,2H),7.13(d,J=9.0Hz,2H),7.26-7.30(m,2H),7.38-7.48(m,5H),7.78(brs,1H),7.86(d,J=8.7Hz,1H)IR(KBr)3444,3269,1710,1533,1487,1269,1244,1199,1174,744,697cm-1 |
I-1320 | mp157-159℃1H NMR(CDCl3)δ1.30(t,J=7.6Hz,3H),2.27(s,3H),2.28(s,3H),2.68(q,J=7.2Hz,2H),3.91(s,3H),5.21(s,2H),6.81-6.97(m,3H),7.14(d,J=7.6Hz,2H),7.25-7.51(m,7H),7.79(brs,1H),7.86(d,J=8.8Hz,1H)IR(KBr)3434,3260,1707,1519,1501,1488,1260,1241,1213,1172,744,697cm-1 |
I-1321 | mp186-187℃1H NMR(CDCl3)δ1.30(t,J=8.4Hz,3H),2.26(s,3H),2.27(s,3H),2.68(q,J=7.5Hz,2H),5.20(s,2H),7.04-7.14(m,6H),7.26-7.50(m,6H),7.79(brs,1H),7.86(d,J=8.7Hz,1H)IR(KBr)3436,3266,1709,1536,1521,1487,1267,1199,1176,744,697cm-1 |
I-1322 | mp136-137℃1H NMR(CDCl3)δ1.32(t,J=7.5Hz,3H),2.28(s,3H),2.30(s,3H),2.70(q,J=7.5Hz,2H),3.13(s,3H),5.19(s,2H),7.12-7.15(m,3H),7.26-7.29(m,3H),7.37-7.50(m,5H),7.80(brs,1H),7.87(d,J=9.0Hz,1H)IR(KBr)3435,1725,1536,1480,1363,1292,1266,1179,1163,1108,7970,895,811,525cm-1 |
I-1323 | mp150-151℃1H NMR(CDCl3)δ2.18(s,3H),2.27(s,3H),5.20(s,2H),7.04-7.14(m,6H),7.26-7.50(m,6H),7.60(d,J=12.0Hz,1H),7.94(brs,1H)IR(KBr)3421,3302,1712,1523,1490,1422,1299,1274,1205,1176,1132,743,697cm-1 |
I-1324 | mp83-84℃1H NMR(CDCl3)δ1.30(t,J=7.6Hz,3H),1.77(s,3H),1.78(s,3H),1.81(s,6H),2.31(s,3H),2.34(s,3H),2.56(q,J=7.6Hz,2H),3.80(d,J=6.4Hz,2H),3.90(s,3H),4.65(d,J=6.2Hz,2H),5.44(d,J=6.2Hz,2H),5.44(t,J=5.2Hz,1H),5.59(t,J=5.4Hz,1H),6.73(d,J=8.0Hz,1H),6.92-6.94(m,3H),7.12-7.20(m,4H)IR(KBr)3428,3374,2964,1607,1519,1494,1458,1311,1256,1239,1139,1036,1002,855,820cm-1 |
I-1325 | mp113-114℃1H NMR(CDCl3)δ1.30(t,J=7.4Hz,3H),1.76(s,3H),1.78(s,3H),1.80(s,3H),1.84(s,3H),2.30(s,3H),2.32(s,3H),2.55(q,J=7.6Hz,2H),3.79(d,J=6.6Hz,2H),4.63(d,J=6.6Hz,2H),5.43(t,J=5.6Hz,1H),5.55(t,J=6.6Hz,1H),5.73(brs,1H),6.72(d,J=8.0Hz,1H),6.83-6.98(m,3H),7.11-7.19(m,4H)IR(KBr)3413,3298,2965,2924,1518,1494,1435,1242,1127,1013,883cm-1 |
I-1326 | mp81-82℃1H NMR(CDCl3)δ1.29(t,J=7.4Hz,3H),1.74(s,3H),1.77(s,3H),1.78(s,3H),1.81(s,3H),2.27(s,3H),2.31(s,3H),2.54(q,J=7.2Hz,2H),3.79(d,J=7.2Hz,2H),4.63(d,J=6.6Hz,2H),5.42(t,J=6.4Hz,1H),5.55(t,J=6.6Hz,1H),6.71(d,J=8.0Hz,1H),7.04-7.19(m,7H)IR(KBr)3413,2969,2912,2856,1613,1520,1492,1295,1261,1127,1004,881,813cm-1 |
I-1327 | mp94-95℃1H NMR(CDCl3)δ1.74(s,3H),1.77(s,6H),1.81(s,3H),2.21(s,3H),2.26(s,3H),3.72(d,J=6.9Hz,2H),4.63(d,J=6.3Hz,2H),5.35(t,J=6.9Hz,1H),5.55(t,J=6.9Hz,1H),6.37-6.48(m,2H),7.01-7.13(m,6H)IR(KBr)3423,2967,2918,1627,1525,1488,1296,1267,1129,981,837,805cm-1 |
I-1328 | mp178-180℃(decomp.)1H NMR(DMSO-d6)δ3.30(s,3H),3.64(s,3H),4.45(s,2H),5.65(s,2H),6.39(s,1H),6.65(dd,J=8.4,2.1Hz,1H),6.74(d,J=2.1Hz,1H),6.84(d,J=8.7Hz,2H),6.99(d,J=8.4Hz,1H),7.43(d,J=8.7Hz,2H),9.26(s,1H)IR(Nujol)3487,3382,1696,1670,1591,1523,1491,1458,1243,1202,1114,1077,1013,937,811cm-1 |
I-1329 | mp205-210℃(decomp.)1H NMR(DMSO-d6)δ3.34(s,3H),3.44(s,3H),3.67(s,3H),4.93(s,2H),6.43(s,1H),6.76(dd,J=8.4,2.1Hz,1H),6.85(d,J=2.1Hz,1H),6.86(d,J=8.7Hz,2H),7.04(d,J=8.4Hz,1H),7.46(d,J=8.7Hz,2H)IR(Nujol)3388,3333,3270,1671,1614,1579,1556,1523,1443,1223,1172,1121,1033,922,813cm-1 |
I-1330 | mp185-187℃1H NMR(CDCl3)δ1.79(t,J=2.6Hz,3H),2.69(m,2H),2.75(s,3H),3.21(s,3H),3.29(s,3H),3.56(s,3H),3.77(s,3H),4.17(t,J=6.6Hz,2H),6.84(s,1H),7.08(d,J=9.0Hz,1H),7.36(dd,J=9.0,2.1Hz,1H),7.38(d,J=8.7Hz,2H),7.40(d,J=2.1Hz,1H),7.68(d,J=8.7Hz,2H)IR(Nujol)1604,1520,1480,1175,1151,1081,1012,971,948,878,840,807cm-1 |
I-1331 | 泡沫1H NMR(CDCl3)δ1.81(t,J=2.4Hz,3H),2.65(m,2H),3.45(s,3H),3.74(s,3H),4.16(t,J=6.6Hz,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.95(m,2H),7.07(brs,1H),7.07(d,J=8.7Hz,2H)IR(Nujol) 3427,1612,1586,1523,1489,1251,1224,1113,1071,1012cm-1 |
I-1332 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.16(m,2H),4.76(m,2H),5.89~6.02(m,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.96(m,2H),7.09(brs,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3433,1612,1588,1523,1489,1286,1248,1224,1175,1113,1070,1011cm-1 |
I-1333 | 泡沫1H NMR(CDCl3)δ3.45(s,3H),3.74(s,3H),4.11(m,2H),4.67(m,2H),5.96~6.12(m,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.92(d,J=8.4Hz,1H),6.96(dd,J=8.4,2.1Hz,1H),7.08(d,J=2.1Hz,1H),7.53(d,J=8.7Hz,2H)IR(Nujol)3434,1612,1588,1523,1489,1285,1248,1224,1174,1112,1070,1011cm-1 |
I-1334 | 泡沫1H NMR(CDCl3)δ1.95(s,3H),3.45(s,3H),3.75(s,3H),4.11(s,2H),4.68(d,J=6.9Hz,2H),5.75(d,J=6.9Hz,1H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.96(s,2H),7.08(s,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3390,1612,1585,1523,1491,1225,1072,1003,822cm-1 |
I-1335 | m.p179-180℃1H NMR(CDCl3)δ1.88(s,3H),3.45(s,3H),3.75(s,3H),4.07(s,2H),4.69(d,J=6.6Hz,2H),5.89(d,J=6.6H2,1H),6.45(s,1H),6.91(d,J=8.7Hz,2H),6.92(d,J=8.4Hz,1H),6.96(dd,J=1.8,8.4Hz,1H),7.07(d,J=1.8Hz,1H),7.53(d,J=8.7Hz,2H)IR(KBr)3392,1609,1584,1523,1492,1226,1116,1072,1002,813,782cm-1 |
I-1336 | 泡沫1H NMR(CD3OD)δ3.38(s,3H),3.67(s,3H),3.88(dd,J=7.8,9.9Hz,1H),4.10(dd,J=3.6,9.9Hz,1H),4.51(m,1H),5.25(dt,J=10.5,1.5Hz,1H),5.44(dt,J=17.4,1.5Hz,1H),6.00(ddd,J=5.4,10.5,17.4Hz,1H),6.43(s,1H),6.79(dd,J=1.8,8.4Hz,1H),6.85(d,J=8.7Hz,2H),6.86(d,J=1.8Hz,1H),6.92(d,J=8.4Hz,1H),7.45(d,J=8.7Hz,2H)IR(KBr)3399,2934,1612,1588,1523,1489,1254,1114,1071,1012,939,816cm-1 |
I-1337 | 泡沫1HNMR(CDCl3)δ3.45(s,3H),3.75(s,3H),4.20(t,J=2.1Hz,2H),4.84(t,J=2.1Hz,2H),6.45(s,1H),6.92(d,J=8.7Hz,2H),6.98(dd,J=2.1,8.4Hz,1H),7.04(d,J=8.4Hz,1H),7.09(d,J=2.1Hz,1H),7.45(d,J=8.7Hz,2H)IR(KBr)3431,1612,1589,1523,1489,1404,1224,1113,1070,1011,939,826cm-1 |
I-1338 | 泡沫1H NMR(CD3OD)δ3.38(s,3H),3.67(s,3H),4.25(d,J=21.0Hz,2H),4.84(d,J=7.5Hz,2H),5.58(dt,J=19.5,7.5Hz,1H),6.43(s,1H),6.79(dd,J=2.1,8.4Hz,1H),6.84(d,J=8.7Hz,2H),6.86(d,J=2.1Hz,1H),6.96(d,J=8.4Hz,1H),7.45(d,J=8.7Hz,2H)IR(KBr)3409,1701,1612,1591,1523,1489,1404,1246,1113,1071,1010,939,816cm-1 |
I-1339 | 泡沫1H NMR(CDCl3)δ3.44(s,3H),3.74(s,3H),4.21(d,J=21.3Hz,2H),4.66(dd,J=1.8,7.5Hz,2H),5.70(dt,J=16.5,7.5Hz,1H),6.45(s,1H),6.95(d,J=8.7Hz,2H),6.96(d,J=8.4Hz,1H),6.98(dd,J=1.5,8.4Hz,1H),7.09(d,J=1.5Hz,1H),7.51(d,J=8.7Hz,2H)IR(KBr)3411,1698,1611,1588,1522,1488,1223,1112,1070,1011,939,825cm-1 |
I-1340 | mp171-172℃1H NMR(CDCl3)δ1.50(s,3H),1.67(s,3H),1.96(s,3H),3.45(s,3H),3.77(s,3H),4.13-4.49(m,2H),5.23-5.30(m,1H),5.59(s,1H),6.13(s,1H),6.47(s,1H),6.92-6.98(m,2H),7.18-7.35(m,3H),7.50-7.57(m,2H)IR(KBr)3390,3140,2935,1640,1523,1401,1240,1119,1070,835,820cm-1 |
I-1341 | mp216.218℃1H NMR(CDCl3+CD3OD)δ1.46(s,3H),1.67(s,3H),1.95(s,3H),2.10(s,3H),3.46(s,3H),4.16-4.47(m,2H),5.21-5.28(m,1H),6.79(s,1H),6.88-6.95(m,2H),7.11-7.27(m,3H),7.45-7.52(m,2H)IR(KBr)3337,3099,2928,1637,1608,1587,1521,1444,1409,1261,1232,1161,836,769,592,540cm-1 |
I-1342 | mp103-105℃1H NMR(CDCl3)δ1.15(d,J=6.8Hz,6H),2.26(s,3H),3.08(sept,J=6.8Hz,1H),4.94(s,1H),5.20(s,2H),6.88(d,J=8.7Hz,2H),7.04-7.07(m,3H),7.12-7.18(m,1H),7.18(s,1H),7.20(d,J=8.7Hz,2H),7.32-7.51(m,5H)IR(KBr)3429,1522,1490,1262,1227,1128,1011,833cm-1 |
I-1343 | mp115-117℃1H NMR(CDCl3)δ1.15(d,J=6.6Hz,6H),1.77(s,3H),1.82(s,3H),2.27(s,3H),3.08(sept,J=6.8Hz,1H),4.64(d,J=6.9Hz,2H),4.86(s,1H),5.56(t,J=6.9Hz,1H),6.89(d,J=8.6Hz,2H),7.03(t,J=8.4Hz,1H),7.05-7.19(m,3H),7.19(s,1H),7.21(d,J=8.6-Hz,2H)IR(KBr)3524,1611,1523,1489,1260,1228,1200,1128,836cm-1 |
I-1344 | mp119-120℃1H NMR(CDCl3)δ1.15(d,J=6.9Hz,6H),2.26(s,3H),3.08(sept,J=6.8Hz,1H),4.79(d,J=6.3Hz,2H),4.85(s,1H),6.25(t,J=6.3Hz,1H),6.89(d,J=8.7Hz,2H),7.01(t,J=8.4Hz,1H),7.07-7.12(m,2H),7.15(dd,J=12.0,2.1Hz,1H),7.18(s,1H),7.20(d,J=8.7Hz,2H)IR(KBr)3425,1610,1523,1488,1300,1263,1300,1263,1227,1134,1038,896cm-1 |
I-1345 | mp109-110℃1H NMR(CDCl3)δ1.34(d,J=6.9Hz,3H),2.24(s,3H),4.00(q,J=6.9Hz,2H),4.77-4.79(m,3H),6.24(t,J=6.3Hz,1H),6.86-6.90(m,2H),6.98-7.19(m,4H),7.47-7.50(m,2H)IR(CHCl3)3596,2927,1612,1523,1493,1476,1388,1299,1259,1173,1127,1049,885,834cm-1 |
I-1346 | mp114-116℃1HNMR(CDCl3)δ1.33(d,J=6.9Hz,3H),1.77(s,3H),1.81(s,3H),2.24(s,3H),4.00(q,J=6.9Hz,2H),4.63(m,2H),4.73(br,1H),5.56(m,1H),6.81(s,1H),6.86-6.90(m,2H),7.00-7.19(m,4H),7.47-4.51(m,2H)IR(CHCl3)3596,2929,2877,1610,1523,1493,1476,1386,1329,1316,1297,1261,1173,1125,1048,992,834cm-1 |
I-1347 | mp144-146℃1H NMR(CDCl3)δ3.20(s,3H),3.40(s,3H),3.75(s,3H),4.74(s,2H),5.19(s,2H),6.44(s,1H),7.05-7.62(m,12H)IR(KBr)3437,1614,1579,1520,1488,1465,1453,1436,1414,1393,1364,1346,1299,1270,1235,1198,1175,1149,1129,1114,1085,1063cm-1 |
I-1348 | mp156-159℃1H NMR(CDCl3)δ2.48(s,3H),3.05(s,3H),3.20(s,3H),3.78(s,3H),4.83(s,2H),5.21(s,2H),6.84(s,1H),7.02-7.67(m,12H)IR(KBr)3430,2940,1607,1522,1481,1452,1419,1389,1365,1294,1273,1230,1200,1176,1151,1132,1080,1011cm-1 |
I-1349 | mp155-156℃1H NMR(CDCl3)δ1.15(t,J=6.9Hz,3H),3.60(q,J=6.9Hz,2H),3.75(s,3H),3.90(s,3H),4.93(bs,1H),5.20(s,2H),5.98(s,1H),6.46(s,1H),6.90-7.05(m,5H),7.26-7.56(m,7H)IR(KBr)3409,2938,1613,1522,1438,1416,1398,1382,1360,1268,1232,1211,1169,1131,1113,1078,1022,1006cm-1 |
I-1350 | mp58-60℃1H NMR(DMSO-d6)δ1.71(s,6H),2.21(s,3H),2.22(s,3H),3.71-3.75(m,2H),5.11(brs,2H),5.25-5.29(m,1H),5.50-5.53(m,1H),6.60-6.63(m,2H),6.66-6.73(m,1H),6.95-7.05(m,6H)IR(KBr)3600-2800(br),1623,1527,1492,1454,1428,1331,1269,1257,1184,1116cm-1 |
I-1351 | mp140-142℃(dec.)1HNMR(CDCl3)δ2.33(s,3H),4.93 (s,1H),5.19(s,2H),6.89(d,J=8.7Hz,2H),7.06(t,J=8.6Hz,1H),7.23(d,J=8.7Hz,2H),7.24-7.50(m,10H)IR(KBr)3400,1609,1529,1490,1269,1243,1005,807,745cm-1 |
I-1352 | mp114-116℃1H NMR(CDCl3)δ1.77(s,3H),1.81(s,3H),2.33(s,3H),4.63(d,J=6.9Hz,2H),4.89(s,1H),5.54(t,J=6.9Hz,1H),6.89(d,J=8.6Hz,2H),7.04(t,J=8.6Hz,1H),7.23(d,J=8.6Hz,2H),7.25-7.43(m,5H)IR(KBr)3368,1609,1526,1490,1271,1241,1131,991,827,811cm-1 |
I-1353 | mp78-79℃1H NMR(CDCl3)δ1.77(s,3H),1.82(s,3H),2.24(s,3H),2.27(s,3H),4.64(d,J=6.6Hz,2H),5.51-5.59(m,1H),6.98-7.20(m,7H),7.28-7.36(m,2H) |
No. | R1 | R2 | R3 | R4 | R5 | R6 | R7 | R8 | R9 | R10 | R11 | R12 | R13 | X | Y |
I-1364 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1355 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1356 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1357 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1358 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1359 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1360 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1361 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1362 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1363 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1364 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1365 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1366 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1367 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1368 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1369 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1370 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1371 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1372 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C≡CMe |
I-1373 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1374 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1375 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1376 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C≡CMe |
I-1377 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1378 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1379 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1380 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1381 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C≡CMe |
I-1382 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1383 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1384 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1385 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1386 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1387 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1388 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CCl2 |
I-1389 | OH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C≡CMe |
I-1390 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1391 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1392 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1393 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C≡CMe |
I-1394 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1395 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1396 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1397 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1398 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1399 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1400 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1401 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1402 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1403 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1404 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1405 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1406 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1407 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1408 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1409 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1410 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1411 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1412 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C≡CMe |
I-1413 | OH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1414 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CCl2 |
I-1415 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C≡CMe |
I-1416 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1417 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1418 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1419 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C≡CMe |
I-1420 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMe | O | -CH2C6H4-4-Me |
I-1421 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1422 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1423 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1424 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C≡CMe |
I-1425 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1426 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1427 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1428 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1429 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1430 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1431 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CMe2 |
I-1432 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1433 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CCl2 |
I-1434 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C≡CMe |
I-1435 | OH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C6H4-4-Me |
I-1436 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CCl2 |
I-1437 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C≡CMe |
I-1438 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1439 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1440 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1441 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C≡CMe |
I-1442 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1443 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1444 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1445 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1446 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C≡CMe |
I-1447 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1448 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1449 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1450 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1451 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1452 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1453 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1454 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CCl2 |
I-1455 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C≡CMe |
I-1456 | OH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C6H4-4-Me |
I-1457 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1458 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1459 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1460 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1461 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1462 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1463 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1464 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CHC≡CMe |
I-1466 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1466 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1467 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1468 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1469 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1470 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1471 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1472 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1473 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1474 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1475 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1476 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1477 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1478 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1479 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1480 | OH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1481 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1482 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1483 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1484 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1485 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1486 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1487 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1488 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1489 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1490 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1491 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1492 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1493 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1494 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1495 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1496 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1497 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1498 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1499 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1500 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1501 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1502 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1503 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1504 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1505 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1506 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1507 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1508 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CCH2 |
I-1509 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C≡CMe |
I-1510 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1511 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1512 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1513 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1514 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C≡CMe |
I-1515 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1516 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1517 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1518 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1519 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C≡CMe |
I-1520 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1521 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1522 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1523 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1524 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1525 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1526 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CMe2 |
I-1527 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1528 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CCl2 |
I-1529 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C≡CMe |
I-1530 | OMs | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1531 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1532 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1533 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C≡CMe |
I-1534 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1535 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1536 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1537 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1538 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1539 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1540 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1541 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1542 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1543 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1544 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1545 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1546 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1547 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1548 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1549 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1550 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1551 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C≡CMe |
I-1552 | OMs | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C6H2-4-Me |
I-1553 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CMe2 |
I-1554 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1555 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CCl2 |
I-1556 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C≡CMe |
I-1557 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1558 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1559 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1560 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C≡CMe |
I-1561 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1562 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1563 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1564 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C≡CMe |
I-1565 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1566 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1567 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1568 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1569 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1570 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1571 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CMe2 |
I-1572 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1573 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CCl2 |
I-1574 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C≡CMe |
I-1575 | OMs | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C6H4-4-Me |
I-1576 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-1577 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1578 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CCl2 |
I-1579 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C≡CMe |
I-1580 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1581 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1582 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C≡CMe |
I-1583 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1584 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1585 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CC2 |
I-1586 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C≡CMe |
I-1587 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1588 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CHCH=CMe2 |
I-1589 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1590 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1591 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1592 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1593 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1594 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CCl2 |
I-1595 | OMs | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C≡CMe |
I-1596 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1597 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1598 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1599 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1600 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1601 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1602 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1603 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1604 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1605 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1606 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-I607 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1608 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1609 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1610 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1611 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1612 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1613 | OMe | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1614 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1615 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1616 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1617 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1618 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1619 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1620 | OMs | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1621 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1622 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1623 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1624 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1625 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1626 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1627 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1628 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1629 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1630 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1631 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1632 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1633 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1634 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1635 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1636 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1637 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1638 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C≡CMe |
I-1639 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1640 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1641 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1642 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C≡CMe |
I-1643 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1644 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1645 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1646 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1647 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C≡CMe |
I-1648 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1649 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1650 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1651 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1652 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1653 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1654 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CCl2 |
I-1655 | F | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C≡CMe |
I-1656 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1657 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1658 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1659 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C≡CMe |
I-1660 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1661 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1662 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1663 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1664 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1665 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1666 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1667 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1668 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1669 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1670 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C4H4-4-Me |
I-1671 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1672 | F | H | H | H | H | H | OMe | OMe | CHOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1673 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1674 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1675 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1676 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1677 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1678 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1679 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C≡CMe |
I-1680 | F | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1681 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CMe2 |
I-1682 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1683 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CCl2 |
I-1684 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C≡CMe |
I-1685 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1686 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1687 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1688 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1689 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C≡CMe |
I-1690 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1691 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1692 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1693 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1694 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C≡CMe |
I-1695 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1696 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1697 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1698 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1699 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1700 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1701 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CMe2 |
I-1702 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1703 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CCl2 |
I-1704 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C≡CMe |
I-1705 | F | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C6H4-4-Me |
I-1706 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-1707 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1708 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CCl2 |
I-1709 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C≡CMe |
I-1710 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1711 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1712 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1713 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C≡CMe |
I-1714 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1715 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1716 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1717 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1718 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C≡CMe |
I-1719 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1720 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1721 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1722 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1723 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1724 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1725 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CMe2 |
I-1726 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1727 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CCl2 |
I-1728 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C≡CMe |
I-1729 | F | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C6H4-4-Me |
I-1730 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1731 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1732 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1733 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1734 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1735 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1736 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1737 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1738 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1739 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1740 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1741 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1742 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1743 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1744 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1745 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1746 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1747 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1748 | F | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1749 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1750 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1751 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1752 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1753 | F | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1754 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1755 | -OCHH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1756 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1757 | -OCHH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1758 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1759 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1760 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OMe | O | -(CH2)2CH=CMe2 |
I-1761 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1762 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1763 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1764 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1765 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1766 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1767 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1768 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1768 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1769 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1770 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CC2 |
I-1771 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1772 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1773 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1774 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1775 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1776 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1777 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1778 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1779 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1780 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1781 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C≡CMe |
I-1782 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1783 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1784 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1785 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1786 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C≡CMe |
I-1787 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1788 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1789 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1790 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CC2 |
I-1791 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C≡CMe |
I-1792 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1793 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1794 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1795 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1796 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1797 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1798 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CMe2 |
I-1799 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1800 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CCl2 |
I-1801 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C≡CMe |
I-1802 | -OCH2O-* | H | H | * | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1803 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1804 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1805 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1806 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C≡CMe |
I-1807 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1808 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1809 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1810 | -OOH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1811 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1812 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1813 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1814 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1815 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1816 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1817 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1818 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1819 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1820 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CCH2 |
I-1821 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1822 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1823 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1824 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1825 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1826 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C≡CMe |
I-1827 | -OCH2O-* | H | H | * | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1828 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CMe2 |
I-1829 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1830 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CCl2 |
I-1831 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C≡CMe |
I-1832 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1833 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1834 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1835 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1836 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C≡CMe |
I-1837 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1838 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1839 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1840 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1841 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C≡CMe |
I-1842 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1843 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1844 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1845 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1846 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1847 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1848 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CMe2 |
I-1849 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1850 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CCl2 |
I-1851 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C≡CMe |
I-1852 | -OCH2O-* | H | H | * | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C6H4-4-Me |
I-1853 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-1854 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1855 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CCl2 |
I-1856 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C≡CMe |
I-1857 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1858 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1859 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1860 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1861 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C≡CMe |
I-1862 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1863 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1864 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1865 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1866 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C≡CMe |
I-1867 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1868 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1869 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1870 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-187 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1872 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1873 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CMe2 |
I-1874 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1875 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CCl2 |
I-1876 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C≡CMe |
I-1877 | -OCH2O-* | H | H | * | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C6H4-4-Me |
I-1878 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1879 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1880 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1881 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1882 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1883 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1884 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1885 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCI2 |
I-1886 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1887 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1888 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1889 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1890 | -OCH2O-* | H | H | * | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1891 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1892 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1893 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1894 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1895 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1896 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1897 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1898 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1899 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1900 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1901 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1902 | -OCH2O-* | H | H | * | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1903 | NMe2 | H | H | H | H | H | OMe | OMe | O | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1904 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1905 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-1906 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1907 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1908 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1909 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1910 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1911 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1912 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1913 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1914 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1915 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1916 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1917 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1918 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1919 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1920 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1921 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1922 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1923 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1924 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-1925 | NMe2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1926 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1927 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1928 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1929 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C≡CMe |
I-1930 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1931 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1932 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1933 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1934 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C≡CMe |
I-1935 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1936 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1937 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1938 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1939 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C≡CMe |
I-1940 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1941 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1942 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1943 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1944 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1945 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1946 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CMe2 |
I-1947 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1948 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CCl2 |
I-1949 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C≡CMe |
I-1950 | NMe2 | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1951 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-1952 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1953 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-1954 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C≡CMe |
I-1955 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1956 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1957 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1958 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1959 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C≡CMe |
I-1960 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1961 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1962 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1963 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-1964 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C≡CMe |
I-1965 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1966 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1967 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-198 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1969 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1970 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1971 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CMe2 |
I-1972 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1973 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CCl2 |
I-1974 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C≡CMe |
I-1975 | NMe2 | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-1976 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CMe2 |
I-1977 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-1978 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CCl2 |
I-1979 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C≡CMe |
I-1980 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C6H4-4-Me |
I-1981 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CMe2 |
I-1982 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-1983 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CCl2 |
I-1984 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C≡CMe |
I-1985 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-1986 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CMe2 |
I-1987 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-1988 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CC2 |
I-1989 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C≡CMe |
I-1990 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-1991 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-1992 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-1993 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-1994 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C≡CMe |
I-1995 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-1996 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CMe2 |
I-1997 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-1998 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CCl2 |
I-1999 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C≡CMe |
I-2000 | NMe2 | H | H | H | H | H | OMe | OMe | Me | H | H | H | H | O | -CH2C6H4-4-Me |
I-2001 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-2002 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2003 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CCl2 |
I-2004 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C≡CMe |
I-2005 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2006 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2007 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2008 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2009 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C≡CMe |
I-2010 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2011 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2012 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2013 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2014 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C≡CMe |
I-2015 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2016 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2017 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2018 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2019 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2020 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2021 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CMe2 |
I-2022 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2023 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CCl2 |
I-2024 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C≡CMe |
I-2025 | NMe2 | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C6H4-4-Me |
I-2026 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2027 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2028 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-2029 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-2030 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2031 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2032 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2033 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2034 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-2035 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C3H4-4-Me |
I-2036 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2037 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2038 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2039 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-2040 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2041 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2042 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2043 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2044 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2045 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2046 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-2047 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2048 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-2049 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-2050 | NMe2 | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-2051 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2052 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-2053 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-2054 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2055 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2056 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2057 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-2058 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2059 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2060 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2061 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2062 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-2063 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2064 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2065 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2066 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2067 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2068 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2069 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-2070 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2071 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-2072 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-2073 | COOH | H | H | H | H | H | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-2074 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2075 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2076 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2CH=CCl2 |
I-2077 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C≡CMe |
I-2078 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2079 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2080 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2081 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2082 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C≡CMe |
I-2083 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2084 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2085 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2086 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2087 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C≡CMe |
I-2088 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2089 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2090 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2091 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2092 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2093 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2094 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CMe2 |
I-2095 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2096 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2CH=CCH2 |
I-2097 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C≡CMe |
I-2098 | COOH | H | H | H | H | H | OMe | OMe | COOH | H | H | H | F | O | -CH2C6H4-4-Me |
I-2099 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2100 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2101 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-2102 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C≡CMe |
I-2103 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2104 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2105 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2106 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2107 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C≡CMe |
I-2108 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2109 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2110 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2111 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2112 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C≡CMe |
I-2113 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2114 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2115 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2116 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2117 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2118 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2119 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CMe2 |
I-2120 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2121 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2CH=CCl2 |
I-2122 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C≡CMe |
I-2123 | COOH | H | H | H | H | H | OMe | OMe | CH2OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-2124 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CMe2 |
I-2125 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2126 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2CH=CCl2 |
I-2127 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C≡CMe |
I-2128 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2129 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2130 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2131 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2132 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C≡CMe |
I-2133 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2134 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2135 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2136 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2CH=CCH2 |
I-2137 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C≡CMe |
I-2138 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2139 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2140 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2141 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2142 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2143 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2144 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CMe2 |
I-2145 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2146 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2CH=CCl2 |
I-2147 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C≡CMe |
I-2148 | COOH | H | H | H | H | H | OMe | OMe | Me | H | H | H | F | O | -CH2C6H4-4-Me |
I-2149 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-2150 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2151 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2CH=CCl2 |
I-2152 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C≡CMe |
I-2153 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2154 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CMe2 |
I-2155 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2156 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2CH=CCl2 |
I-2157 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C≡CMe |
I-2158 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2159 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2160 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2161 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2162 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C≡CMe |
I-2163 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2164 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2165 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2166 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2167 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2168 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2169 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CMe2 |
I-2170 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2171 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2CH=CCl2 |
I-2172 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C≡CMe |
I-2173 | COOH | H | H | H | H | H | OMe | OMe | H | H | H | H | F | O | -CH2C6H4-4-Me |
I-2174 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2175 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -(CH2)2CH=CMe2 |
I-2176 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CCl2 |
I-2177 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C≡CMe |
I-2178 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H4-4-Me |
I-2179 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2180 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2181 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2182 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C≡CMe |
I-2183 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | OMs | O | -CH2C6H4-4-Me |
I-2184 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CMe2 |
I-2185 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -(CH2)2CH=CMe2 |
I-2186 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2CH=CCl2 |
I-2187 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C≡CMe |
I-2188 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | COOH | O | -CH2C6H4-4-Me |
I-2189 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CMe2 |
I-2190 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -(CH2)2CH=CMe2 |
I-2191 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2CH=CCl2 |
I-2192 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C≡CMe |
I-2193 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | CH2OH | O | -CH2C6H4-4-Me |
I-2194 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CMe2 |
I-2195 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -(CH2)2CH=CMe2 |
I-2196 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2CH=CCl2 |
I-2197 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C≡CMe |
I-2198 | COOH | H | H | H | H | F | OMe | OMe | OH | H | H | H | F | O | -CH2C6H4-4-Me |
I-2199 | NO2 | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2200 | OMs | NO2 | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2201 | OMs | H | H | H | H | H | OMe | OMe | H | NO2 | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2202 | CN | H | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2203 | OMs | CN | H | H | H | H | OMe | OMe | H | H | H | H | OMs | O | -(CH2)2CH=CMe2 |
I-2204 | OH | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2CH=CMe2 |
I-2205 | OH | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2C6H5 |
I-2206 | OH | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2207 | OH | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2C6H5 |
I-2208 | OH | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2C6H6 |
I-2209 | OH | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2210 | OH | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2C6H5 |
I-2211 | OH | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2212 | OH | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2C6H5 |
I-2213 | OH | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | OH | O | -CH2CH=CMe2 |
I-2214 | OH | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2215 | OH | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2C6H5 |
I-2216 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2217 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H5 |
I-2218 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2219 | OH | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2C6H5 |
I-2220 | OMs | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2CH=CMe2 |
I-2221 | OMs | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2C6H5 |
I-2222 | OMs | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2223 | OMs | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2C6H5 |
I-2224 | OMs | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2225 | OMs | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2C6H5 |
I-2226 | OMs | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2227 | OMs | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2C6H6 |
I-2228 | OMs | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-2229 | OMs | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2C6H5 |
I-2230 | OMs | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2231 | OMs | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2C6H5 |
I-2232 | OMs | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | OH | O | -CH2CH=CMe2 |
I-2233 | OMs | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2234 | OMs | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2C6H6 |
I-2235 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2236 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H5 |
I-2237 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2238 | OMs | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2C6H6 |
I-2239 | CF3 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2CH=CMe2 |
I-2240 | CH3 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2C6H6 |
I-2241 | CF3 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2242 | CF3 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2C6H6 |
I-2243 | CF3 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2244 | CF3 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2C6H5 |
I-2245 | CF3 | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2246 | CF3 | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2C6H5 |
I-2247 | CF3 | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-2248 | CF3 | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2C6H5 |
I-2249 | CF3 | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2250 | CF3 | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2C6H5 |
I-2251 | CF3 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | OH | O | -CH2CH=CMe2 |
I-2252 | CF3 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | OH | O | -CH2C6H5 |
I-2253 | CF3 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2254 | CF3 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2C6H6 |
I-2255 | CF3 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2256 | CF3 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H5 |
I-2257 | CF3 | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2258 | CF3 | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2C6H5 |
I-2259 | NH2 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2CH=CMe2 |
I-2260 | NH2 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | OH | O | -CH2C6H5 |
I-2261 | NH2 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2262 | NH2 | H | H | H | H | H | OMe | OMe | OMs | H | H | H | NH2 | O | -CH2C6H5 |
I-2263 | NH2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2264 | NH2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OH | O | -CH2C6H5 |
I-2265 | NH2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2266 | NH2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | NH2 | O | -CH2C6H5 |
I-2267 | NH2 | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2CH=CMe2 |
I-2268 | NH2 | H | H | H | H | H | Me | Me | H | H | H | H | OH | O | -CH2C6H5 |
I-2269 | NH2 | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2270 | NH2 | H | H | H | H | H | Me | Me | H | H | H | H | NH2 | O | -CH2C6H5 |
I-2271 | NH2 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | OH | O | -CH2CH=CMe2 |
I-2272 | NH2 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | OH | O | -CH2C6H6 |
I-2273 | NH2 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2274 | NH2 | H | H | H | H | H | OMe | OMe | NH2 | H | H | H | NH2 | O | -CH2C6H5 |
I-2275 | NH2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2CH=CMe2 |
I-2276 | NH2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | OH | O | -CH2C6H5 |
I-2277 | NH2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2CH=CMe2 |
I-2278 | NH2 | H | H | H | H | H | OMe | OMe | OH | H | H | H | NH2 | O | -CH2C6H5 |
I-2279 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2280 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2281 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | NMe | Me |
I-2282 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2283 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2284 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | NH | -CH2CH=CMe2 |
I-2285 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2286 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | NMe | Me |
I-2287 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CMe2 |
I-2288 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | H | O | -CH2CH=CCl2 |
I-2289 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2290 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2291 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | NMe | Me |
I-2292 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2293 | -NHCH2CH=CMe2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2294 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2295 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2296 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | NMe | Me |
I-2297 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2298 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2299 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2300 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2301 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | NMe | Me |
I-2302 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2303 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2304 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2305 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2306 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | NMe | Me |
I-2307 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2308 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2309 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2330 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2331 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | NMe | Me |
I-2332 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2333 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2334 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2335 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2336 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | NMe | Me |
I-2337 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | H | O | -CH2CH=CMe2 |
I-2338 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2339 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2340 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2341 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | NMe | Me |
I-2342 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2343 | -NHCH2CH=CMe2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2344 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2345 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2346 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | NMe | Me |
I-2347 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2348 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2349 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | NH | -CH2CH=CMe2 |
I-2350 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2351 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | NMe | Me |
I-2352 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CMe2 |
I-2353 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CCl2 |
I-2354 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2355 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2356 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | NMe | Me |
I-2357 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2358 | -NHCH2CH=CMe2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2359 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2360 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2361 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | NMe | Me |
I-2362 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2363 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2364 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2365 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2366 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | NMe | Me |
I-2367 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2368 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2369 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2370 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2371 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | NMe | Me |
I-2372 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2373 | -NHCH2CH=CMe2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2374 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2375 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2376 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | NMe | Me |
I-2377 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2378 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2379 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | NH | -CH2CH=CMe2 |
I-2380 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2381 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | NMe | Me |
I-2382 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CMe2 |
I-2383 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CCl2 |
I-2384 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2385 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2386 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | NMe | Me |
I-2387 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2388 | -NH2 | H | F | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2389 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2390 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2391 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | NMe | Me |
I-2392 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2393 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2394 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2395 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2396 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | NMe | Me |
I-2397 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2398 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2399 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2400 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2301 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | NMe | Me |
I-2302 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2303 | -NH2 | H | F | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2304 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2305 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2306 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | NMe | Me |
I-2307 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2308 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2309 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2310 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2311 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | NMe | Me |
I-2312 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2313 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2314 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2315 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2316 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | NMe | Me |
I-2317 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2318 | -NH2 | H | F | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2319 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-230 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2321 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | NMe | Me |
I-2322 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2323 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2324 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | NH | -CH2CH=CMe2 |
I-2325 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | NH | -(CH2)2CHMe2 |
I-236 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | NMe | Me |
I-2327 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CMe2 |
I-2328 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CCl2 |
I-2329 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2330 | -NH2 | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2331 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | NMe | Me |
I-2332 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2333 | -NH2 | H | F | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2334 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2335 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2336 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | NMe | Me |
I-2337 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2338 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2339 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2340 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2341 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | NMe | Me |
I-2342 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2343 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CC2 |
I-2344 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2345 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2346 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | NMe | Me |
I-2347 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2348 | -NH2 | H | F | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2349 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2350 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2351 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | NMe | Me |
I-2352 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2353 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2354 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | F | H | NH | -CH2CH=CMe2 |
I-2355 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2356 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | F | H | NMe | Me |
I-2357 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CMe2 |
I-238 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CCl2 |
I-2359 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2360 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2361 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | NMe | Me |
I-2362 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2363 | -NHCH2CH=CMe2 | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2364 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2365 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2366 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | NMe | Me |
I-2367 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2368 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2369 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2370 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2371 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | F | H | NMe | Me |
I-2372 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2373 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2374 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2375 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2376 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | NMe | Me |
I-2377 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2378 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2379 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2380 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2381 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | NMe | Me |
I-2382 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2383 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2384 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2385 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-236 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | F | H | NMe | Me |
I-2387 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2388 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2389 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2390 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2391 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | NMe | Me |
I-2392 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2393 | -NHCH2CH=CMe2 | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2394 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2395 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2396 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | NMe | Me |
I-2397 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2398 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2399 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | F | H | NH | -CH2CH=CMe2 |
I-2400 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2401 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | F | H | NMe | Me |
I-2402 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CMe2 |
I-2403 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CCl2 |
I-2404 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2405 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2406 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NMe | Me |
I-2407 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2408 | -NHCH2CH=CMe2 | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2409 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2410 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2411 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | NMe | Me |
I-2412 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2413 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2414 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2415 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2416 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | NMe | Me |
I-2417 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2418 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CC2 |
I-2419 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2420 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2421 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | NMe | Me |
I-2422 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2423 | -NHCH2CH=CMe2 | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2424 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2425 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2426 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | NMe | Me |
I-2427 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2428 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2429 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | F | H | NH | -CH2CH=CMe2 |
I-2430 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2431 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | F | H | NMe | Me |
I-2432 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CMe2 |
I-2433 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | F | H | O | -CH2CH=CCl2 |
I-2434 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2435 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2436 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | NMe | Me |
I-2437 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2438 | -OMe | H | H | H | H | Me | Me | Me | H | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2439 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2440 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2441 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | NMe | Me |
I-2442 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2443 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2444 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2445 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2446 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | F | H | NMe | Me |
I-2447 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2448 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2449 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2450 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2451 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | NMe | Me |
I-2452 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2453 | -OMe | H | H | H | H | H | Me | OMe | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2454 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2455 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2456 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | NMe | Me |
I-2457 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2458 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2459 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2460 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2461 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | F | H | NMe | Me |
I-2462 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2463 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2464 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2465 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2466 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | NMe | Me |
I-2467 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2468 | -OMe | H | H | H | H | Me | H | Me | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2469 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2470 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2471 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | NMe | Me |
I-2472 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2473 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2474 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | F | H | NH | -CH2CH=CMe2 |
I-2475 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2476 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | F | H | NMe | Me |
I-2477 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CMe2 |
I-2478 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | F | H | O | -CH2CH=CCl3 |
I-2479 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2480 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2481 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | NMe | Me |
I-2482 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2483 | -OMe | H | H | H | H | H | Me | Me | Me | H | H | H | OEt | O | -CH2CH=CCl2 |
I-2484 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -CH2CH=CMe2 |
I-2485 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | NH | -(CH2)2CHMe2 |
I-2486 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | NMe | Me |
I-2487 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CMe2 |
I-2488 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OMe | O | -CH2CH=CCl2 |
I-2489 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -CH2CH=CMe2 |
I-2490 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | NH | -(CH2)2CHMe2 |
I-2491 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | NMe | Me |
I-2492 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CMe2 |
I-2493 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | F | H | O | -CH2CH=CCl2 |
I-2494 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -CH2CH=CMe2 |
I-2495 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | NH | -(CH2)2CHMe2 |
I-2496 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | NMe | Me |
I-2497 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CMe2 |
I-2498 | -OMe | H | H | H | H | H | OMe | OEt | OH | H | H | H | OEt | O | -CH2CH=CCl2 |
表中,-OCH2O-*及*表示一起形成环。
试验例1对于小鼠脾细胞体外抑制促分裂原反应的效果
在96个孔的微型滴定板的各孔中加入使C3H/HeN小鼠脾细胞5×105个浮游在含有0.1ml的10%牛胎血清的RPMI 1640培养基(加入碳酸氢钠2mM、青霉素50单位/ml、链霉素50μg/ml及2-巯基乙醇5×10-5M)中的物质,在各孔中以各种浓度加入作为促分裂原的伴刀豆球蛋白A(ConA)5μg/ml或脂多糖(LPS)10μg/ml和本发明的化合物,将各孔的最终容量作成0.2ml。各本发明的化合物溶解在二甲基亚砜(DMSO)中,用上述RPMI 1640培养基稀释,添加到最终浓度达到100ng/ml以下。在将96孔微型滴定板放在湿度为100%、二氧化碳为5%、空气为95%的培养器内、在37℃下培养3天。然后,在各孔中加入6mg/ml的MTT〔3-(4,5-二甲基噻唑-2-基)-2,5-,二苯基四唑溴鎓〕(西格玛制)溶液25μl,在37℃下,在相同条件下培养4小时。培养终了后,在生成的甲_中加入20%的十二烷基磺酸钠(SDS)的0.02N-盐酸溶液50μl,在37℃下放置24小时、溶解。用装有570nm的滤波器免疫读出仪(Inter Med)测定与活细胞数成比例地生成的甲_的吸光度(OD)(免疫方法杂志(TheJournal of immnological method)、65卷、55-63页(1983年))。从本发明的化合物浓度和吸光强度的关系,算出阻止50%的细胞增殖浓度(IC50值)。
试验2对于EL4细胞的抗细胞增殖效果
在96孔微型滴定板的各孔中,以4×104个/0.1ml的比例,加入小鼠胸腺肿瘤株EL4细胞,添加本发明的化合物0.1ml使其达到0~5000ng/ml。培养3天,用试验例1表示的MTT法算出该IC50。
试验例1及2的结果如表328~表329所示。表328
表329
化合物 | ConAIC50(ng/ml) | LPSIC50(ng/ml) | EL-4IC50(ng/ml) |
I-1 | 0.86 | 1.92 | 8.56 |
I-9 | <20 | <20 | <20 |
I-12 | 1.3 | 2.8 | 46.2 |
1-22 | 5.62 | 4.26 | 6.2 |
I-35 | 19.5 | 39.4 | 140 |
I-40 | 6.1 | 16.5 | 37.4 |
I-41 | 0.73 | 1.74 | 4.89 |
I-46 | 10.6 | 23.9 | 67.5 |
I-49 | 8.89 | 16.2 | 31.7 |
I-50 | 3.83 | 9.2 | 11.9 |
I-51 | 6.6 | 14.7 | 70.0 |
I-59 | 8.5 | 22.4 | 140 |
I-62 | 29.2 | 25 | 23.4 |
I-63 | 13 | 27 | 16 |
I-66 | 0.22 | 0.35 | 0.48 |
I-71 | 4.56 | 14.2 | 31.2 |
I-101 | 0.8 | 0.5 | 1.8 |
I-103 | 3.4 | 3.7 | 4.6 |
I-104 | 3.0 | 3.1 | 4.8 |
I-106 | 0.6 | 0.4 | 2.7 |
I-107 | 0.6 | 0.7 | 12 |
I-121 | 0.8 | 1.2 | 0.8 |
I-163 | <20 | <20 | <20 |
I-173 | <20 | <20 | <20 |
I-175 | <20 | 29.4 | <20 |
I-187 | 12.0 | 25.1 | 36.2 |
I-211 | <20 | <20 | <20 |
I-248 | <10 | <10 | 312 |
I-250 | <10 | <10 | 88.3 |
I-251 | <10 | <10 | 97.4 |
I-255 | <20 | <20 | <20 |
I-256 | <20 | 28.7 | 310 |
I-275 | 6.34 | 13.5 | 100 |
I-276 | 1.8 | 3.1 | 200 |
I-299 | 5.53 | 7.85 | 13.6 |
I-301 | 7.06 | 11.0 | 15.8 |
I-360 | <20 | <20 | 99.8 |
I-361 | <20 | <20 | 124 |
I-418 | 255 | 497 | >10000 |
I-427 | 255 | 497 | >10000 |
I-457 | <20 | <20 | 205 |
I-466 | <20 | <20 | 46 |
I-484 | 14.7 | 32.2 | 91.4 |
I-513 | 6.89 | 11.1 | 61.8 |
I-525 | 0.76 | 1.11 | 5.0 |
I-639 | 4.59 | 6.25 | 50 |
I-661 | 0.67 | 1.28 | 50 |
I-739 | 18.8 | 20.7 | 430 |
I-742 | 10 | 20 | 45.2 |
I-758 | 6.78 | 9.63 | 55.1 |
I-773 | 8.45 | 12.6 | 92.9 |
I-797 | 1.75 | 3.71 | 26.5 |
I-834 | 36 | 46 | 226 |
I-839 | 1.48 | 1.87 | 20.7 |
I-840 | 5.31 | 6.94 | 31.9 |
I-878 | 14.1 | 27.4 | 194 |
I-880 | 23.0 | 41.1 | 105 |
I-892 | <0.2 | <0.2 | 1.41 |
I-893 | 0.49 | 1.05 | 7.06 |
化合物 | ConAIC50(ng/ml) | LPSIC50(ng/ml) | EL-4IC50(ng/ml) |
I-907 | 23.4 | 44.5 | 82.7 |
I-908 | 0.45 | 0.86 | 3.50 |
I-909 | <20 | <20 | 20 |
I-931 | 2.93 | 5.76 | 4.37 |
I-934 | 16.1 | 22.2 | 52.7 |
I-943 | 2.97 | 4.89 | 46.8 |
I-962 | 12.1 | 16.3 | 20.4 |
I-970 | <20 | <20 | 50.3 |
I-976 | 17.7 | 34.2 | 330 |
I-981 | 14.9 | 27.1 | >100 |
I-982 | 2.0 | 3.75 | 55.3 |
I-988 | 0.2 | 0.31 | 1.23 |
I-993 | 5.10 | 7.54 | 13.8 |
I-995 | 20.9 | 25.2 | 49.2 |
I-1006 | 8.66 | 12.3 | 33.0 |
I-1007 | 8.05 | 10.4 | 13.1 |
I-1017 | 9.74 | 16.7 | 72.9 |
I-1031 | <20 | 21.2 | 41.7 |
I-1040 | 1.80 | 5.31 | 1.85 |
I-1043 | 2.19 | 3.27 | 9.70 |
I-1058 | 21.2 | 30.2 | 48.8 |
I-1066 | 3.91 | 4.87 | 20.6 |
I-1095 | 6.90 | 9.57 | 34.2 |
I-1103 | 4.7 | 6.9 | 31.4 |
I-1107 | 5.8 | 9.1 | 34.1 |
I-1115 | <20 | <20 | <20 |
I-1121 | 3.12 | 9.0 | 18.6 |
I-1123 | 0.80 | 2.00 | 3.9 |
I-1124 | 94 | 272 | >10000 |
I-1126 | 79 | 234 | >10000 |
I-1127 | 44 | 111 | 412 |
I-1128 | 5.00 | 11.4 | 26.0 |
I-1135 | 1.00 | 2.70 | 11.7 |
I-1160 | 10.6 | 14.1 | 97.4 |
I-1161 | 2.4 | 4.2 | 33.2 |
I-1162 | 0.65 | 1.95 | 30.9 |
I-1167 | 0.08 | 0.23 | 8.1 |
I-1168 | 0.26 | 0.54 | 12.5 |
I-1171 | 0.63 | 0.64 | 27.5 |
I-1172 | 13.1 | 19.4 | >100 |
I-1173 | 16.4 | 31.1 | >100 |
I-1177 | 12.2 | 20.8 | 47.2 |
I-1191 | 0.16 | 0.66 | 22.8 |
I-1193 | 1.46 | 5.3 | 50 |
I-1203 | 14.1 | >100 | 43.5 |
I-1212 | 12.87 | 24.2 | 85.0 |
I-1217 | <20 | <20 | <20 |
I-1227 | 197 | 423 | >10000 |
I-1229 | 5.95 | 8.05 | 20.4 |
I-1230 | 12.0 | 15.3 | 5.22 |
I-1232 | 3.77 | 4.93 | 15.1 |
I-1240 | 2.50 | 3.34 | 11.8 |
I-1248 | 25.9 | 36.8 | 118 |
I-1250 | 0.68 | 1.35 | 2.90 |
I-1251 | 6.30 | 10.7 | 27.8 |
I-1263 | <20 | <20 | 29.8 |
I-1271 | 0.10 | 0.32 | 1.66 |
I-1274 | 0.33 | 1.38 | 1.44 |
I-1276 | <20 | 31.3 | 105 |
I-1277 | <20 | <20 | <20 |
I-1278 | <20 | <20 | 41.7 |
I-1284 | <20 | <20 | <20 |
I-1286 | <20 | <20 | <20 |
I-1289 | <20 | <20 | <20 |
I-1290 | <20 | <20 | 27.3 |
I-1295 | <20 | <20 | <20 |
I-1296 | <20 | <20 | 39.7 |
由上述结果表明,本发明的化合物具有免疫抑制作用及抗过敏性作用。
试验例3 对于抗牛γ球蛋白(BGG)的抗体产生抑制效果
对于BALB/c小鼠(雄性、6-8周龄),在免疫开始日及第7天后,将BGG 50μg接种在背部皮下,诱导免疫反应。将本发明的化合物溶解或悬浮在N,N-二甲基乙酰胺中后,用三甘醇(miglyo1)8/2中性油稀释,以适当的给药量从免疫开始的第二天连日经口(PO)给药。作为对照组,以小鼠体重的200分之一的量给与三甘醇。第21天后从各小鼠采血,分离血清。血清中的BGG特异的IgE是通过作成涂层BGG的板后,用三明治ELISA法进行测定的。本发明的化合物的效果评定是从与对照组血清所示的吸光强度相同,显示吸光强度的血清的稀释倍率算出该IgE抑制率。其结果如表330所示。
表330
化合物 | 给药量(mg/kg) | 抗原特异的IgE抑制率(%) |
I-525 | 100 | >95 |
I-915 | 100 | >99 |
I-892 | 5 | >99 |
I-963 | 50 | >99 |
I-1031 | 100 | >99 |
I-1093 | 100 | >99 |
试验例4对于抗卵白蛋白(OVA)IgE抗体的产生抑制效果
1)动物
使用从日本SLC(静冈)购入的BALB/c小鼠(雌性、8~10周龄)及Wistar系小鼠(雌性、8~10周龄)。
2)免疫方法
将卵白蛋白(OVA)2μg和氢氧化铝凝胶(2mg)悬浮在生理食盐水的溶液0.2ml注入到BALB/c小鼠的腹腔内,进行免疫。第10天后从心脏采血,分离血清,到测定IgE抗体价的期间要保存在-40℃下。
3)化合物
本发明的化合物溶解或悬浮在N-二甲基乙酰胺中后,每1只小鼠经口给药用三甘醇油8/2中性油稀释20倍的溶液0.1ml。从免疫之日,到采血的前1日连续进行给药,作为对照,将IPD-1151-T(Jpn.Pharmacol.(1993)61、31-39记载的化合物)及化合物No.36(J.Med.Chem.(1997)40:395-407记载的化合物36)进行相同的试验。
4)抗OVA IgE抗体效价(PCA效价)的测定
用生理食盐水将得到的小鼠血清作成稀释2倍系列,将其预先剃毛后,在Wistar系大鼠的背部皮内各注射50μg。24小时后,将含有OVA1mg和依文恩兰色素5mg的生理食盐水溶液0.5ml注入到静脉内,引起受动皮肤过敏性反应(PCA)。在30分钟后,评定显示色素斑直径为5mm以上的PCA反应阳性的血清的最大稀释倍率,将该稀释倍率的Log2作为PCA效价。例如若某血清稀释到27倍,呈现PCA阳性反应时,其小鼠的抗OVA IgE抗体价就成为7。其结果如表331所示。表331
化合物 | 用量(mg/kg) | PCA效价 |
I-484 | 40 | <0 |
I-839 | 40 | 2.4** |
I-851 | 40 | 1.8** |
I-892 | 40 | <0 |
I-893 | 40 | 2.5** |
I-908 | 40 | 3.4** |
I-915 | 40 | <0 |
I-925 | 40 | 1** |
I-928 | 40 | <0 |
I-948 | 40 | 2.6** |
I-957 | 40 | 4.5** |
I-962 | 40 | <0 |
I-963 | 40 | 3.6** |
I-988 | 40 | 0.8** |
I-1031 | 40 | 4.4** |
I-1043 | 40 | 4.8** |
I-1066 | 40 | <0 |
I-1072 | 40 | 0.8** |
I-1095 | 40 | <0 |
I-1123 | 40 | 2.4** |
I-1135 | 40 | 4.8** |
I-1167 | 40 | 4.4** |
I-1171 | 40 | <0 |
I-1177 | 40 | 3.6** |
I-1229 | 40 | <0 |
I-1232 | 40 | 1.8** |
I-1242 | 40 | 2.8** |
I-1258 | 40 | 1.2** |
I-1271 | 40 | <0 |
IPD-1151-T | 50 | 9.8 |
N0.36 | 10 | 10.4 |
从上述结果可评定本发明的化合物具有抗体产生抑制效果。
试验例5对于使用人体淋巴细胞的抗体产生的抑制效果
1.实验方法
1)人体末梢血
人体末梢血液是从健康的成人男性的静脉,用加入肝素(最终浓度1.5%)的塑料制注射器采血,采血后立即用于淋巴细胞的采取。
2)培养基
在RPMI培养基(日水制药)中,在56℃下,30分钟灭活的胎牛血清(Fetal Bovine Serum、Hyclone Lab.)10%、青霉素(100units/ml)及链霉素(100μg/ml)(GIBCO)进行使用。
3)化合物
将本发明的各化合物(I-839)溶解在二甲基亚砜(Nakaraitest)中,以达到2μg/ml,然后,用培养基稀释,作成最终浓度0.01pg/ml-10μg/ml。作为对照,将No.36进行相同试验。
4)人体淋巴细胞
对人体末梢血等量地层叠在装入Ficoll-Hypaqwe混合溶液(大日本制药(大阪)Mono-Poly resolving medium)的管中,在300×g、15℃下,离心分离30分钟,得到淋巴细胞层。将收集了的细胞浮游液用灭菌的Hanks’液(日水制药)进行离心洗涤后,加入灭菌蒸馏水。在30秒钟后等量加入浓缩2倍的Hanks’液,除去混入红血球。通过尼龙筛孔后,将进一步离心洗涤了的物质作成人体淋巴细胞,用于实验。
5)由于B细胞刺激,诱导产生IgE抗体
在96孔培养板(住友bakelite)中,每个孔中接种人体淋巴细胞,使达到2×105Cells,添加化合物及抗人体CD40抗体(Pharmingen,2μg/ml)、人重组白细胞介素-4(IL-4)(Genzyme,0.1μg/ml)、人重组白细胞介素-10(IL-10)(Genzyme,0.2μg/ml),在37℃下,5%CO2存在下培养(0.2ml/well)。在培养10天后,通过特异的ELISA法定量产生在上清液中的抗体量。
6)IgE抗体的定量
IgE的定量使用了市售的试剂盒MESACUP IgE试验仪(医学生物学研究所)。实验的方法根据使用说明书,用进行三次实验,求出平均值。
7)IgG、IgM抗体的定量
用ELISA法进行测定。在96孔板(Nunc)中加入50μl的1μg/ml的F(ab′)2山羊抗人IgG+A+M(H+L)(ZYMED Laboratories),在4℃下涂敷1夜。第2天,用0.05%Tween/PBS(PBST)溶液洗涤2次后,加入100μl的0.5%明胶/PBST,在室温下封闭2小时。用PBST洗涤3次后,加入100μl的用PBS稀释的样品或各种浓度的人血浆IgG标准液或IgM标准液(BiopurAG,Switzerland),在室温下反应1小时。用PBST洗涤3次后,添加将过氧化物酶标记的抗人体IgG抗体或抗人体IgM抗体(Southern Biotechnology,Birminham),用PBS稀释成1/2000的溶液100ml,在室温下反应1小时。用PBST洗涤4次后,加入底物邻苯二胺二氯化物100μl,在使其发色30分钟后,加入50μl的2N-HCl后,停止反应。将其用微板读数器进行测定(492nm)、从标准液的检量线,算出IgG及IgM的量。
2.结果
结果如图1及图2所示。本发明的化合物(I-839),对于IgE抗体显示了选择性地抑制作用,其作用比产生IgG抑制作用强2000倍以上,比IgM强30000倍以上。表332总结了代表性化合物的产生抗体作用。
表332
化合物 | IC50(ng/ml) | ||
IgE | IgG | IgM | |
I-839I-892I-121I-988I-893 | <0.00001<0.00001<0.0001<0.00001<0.00001 | 0.027<0.00001<0.0001<0.00001<0.0001 | 0.37>1>1>1>1 |
试验例6 小鼠脾脏淋巴细胞抗体产生的抑制作用
1.实验方法
1)动物
使用BALB/c(nu/nu)小鼠是从日本SLC(静冈)购入的7周龄雌性小鼠。
2)培养基
在RPMI培养基(日水制药)中添加在56℃下30分钟灭活的胎牛血清(Fetal Bovine Serum.Hyclone Lab.)10%、青霉素(100units/ml)及链霉素(100μg/ml)(GIBCO)使用。
3)化合物
各化合物溶解在二甲基亚砜(Nakairtesk)中达2μg/ml,然后,用培养基稀释,使最终浓度为0.1pg/ml-10μg/ml。
4)小鼠脾脏淋巴细胞
摘出小鼠的脾脏,放在装有Hanks’液的培养皿上,挤碎脾脏后,从脏器内挤出细胞,通过金属筛(200目)。在将收集的细胞浮游液用灭菌的Hanks’液(日水制药)离心洗涤后,加入灭菌蒸馏水,在30秒钟后等量加入2倍浓缩的Hanks’液,除去混入红血球。通过尼龙筛后,将进一步离心洗净的物质作成小白鼠脾脏淋巴细胞,用于实验。
5)诱导由于B细胞刺激而产生IgE抗体
在96孔培养板(住友Bakelite)中每1个孔接种小白鼠脾脏淋巴球达2×105cells,添加化合物及脂多糖(DIFCO Lab.、2μg/ml)、小白鼠重组体内白细胞素-4(IL-4)(Genzyme、50ng/ml),在37℃、5%CO2存在下培养(0.2ml/孔)培养10天后,通过特殊的ELISA法定量在上清液中产生的抗体量。
6)IgE抗体的定量
IgE的定量是使用市售的小鼠IgE EIA试剂盒(yamasa酱油)进行的。实验方法是按照使用说明书,用重复三次进行试验,求出平均值。
7)IgG1、IgG2a、IgM抗体的定量
在96孔板中添加50μl的10μg/ml的Goat Anti-Mouse Ig(IgM+G+A、H+L)(Southem Biotechnology Birmingham)、在4℃下涂敷1夜。第2天用PBST溶液洗涤2次后,加入100μl的0.5%明胶/PBST,在室温下封闭2小时。用PBST洗涤3次后,添加100μl的用PBS稀释的培养上清液及各种浓度的抗体标准液(Mouse IgGlStandard、Mouse IgG2a Standard、Mouse IgM Standard、BETHYL Laboratories),反应1小时。用PBST洗涤3次后,添加100μl的碱性磷酸酶标识的抗小鼠IgG1、IgG2a或IgM抗体(SouthernBiotechnology,Birmingham)的稀释液,在室温下反应1小时。用PBST洗涤4次后,加入底物对硝酸苯基磷酸二钠(Nitrophenyl Phosphate,Disodium),30分钟后,加入5N-NaOH,停止反应。用微板读出器测定板(405nm),从检量线算出抗体量。另外,小鼠的样品及标准液的稀释,使用10%FCS/PBS。
2.结果
结果如图3所示。从图中,表明(I-967)只表示对于IgG1、IgG2a、IgM抗体在1000ng/ml以上显示抑制作用,但对于产生IgE抗体在0.01以上,浓度依存地抑制。表333表示代表性化合物对产生IgE、IgM、IgG1、IgG2a阻碍作用。
表333
化合物 | IC50(ng/ml) | |||
IgE | IgG1 | IgG2a | IgM | |
I-73 | 0.044 | 2600 | 4900 | 4200 |
I-963 | 0.00026 | 510 | 3600 | 3500 |
I-967 | 0.1 | 3500 | 3600 | >10000 |
试验例7 对于吸入抗原的气管内炎症性细胞浸润的抑制作用
1.实验方法
1)动物
使用从日本SLC(静冈)购入的BALB/c小鼠(雌性、8-11周龄)。
2)致敏方法及抗原攻击
将卵白蛋白(OVA;Grade V、SIGMA)2μg和氢氧化铝凝胶2mg,悬浮在生理食盐水中的溶液0.2ml注射在腹腔内、免疫,进而,在2周后,将2μg的OVA的生理食盐水溶液0.2ml注射到腹腔内、追加免疫。在1周后,将小鼠1只1只地放在喷雾容器(设有12根内径4.8cm、高12cm的圆筒型筒的,内径24.5cm、有效内高20cm的气密聚碳酸酯容器)的筒中,使用超声波式喷雾器(欧母龙、NE-U12),吸入20分钟的5%卵白蛋白(Grade III、SIGMA)的生理食盐水溶液,抗原攻击。
3)本发明化合物的给药
将本发明的化合物(I-963)溶解在N-二甲基乙酰胺(ナカラテスク)中后,将用三甘醇8/2中性油(Mitsuba贸易)稀释20倍的溶液经口给药达40mg/kg。从追加免疫日到洗涤支气管肺泡的前1日连续给药9天。
4)支气管肺泡的洗涤(BAL)
诱发抗原的48小时后,在乙醚麻醉下从心脏进行全采血。接着,在气管中装入插管,注入0.3ml的PBS溶液、回收,进而,用重新注入0.3ml、回收的方法,将气管内反复洗涤共5次(共1.5m1)。
5)BAL溶液中的总细胞数的测定及炎症细胞的分类
用染色(チユルカ)溶液将BAL溶液的一部分染色,算出总细胞数后,将BAL溶液中的细胞通过细胞甩片(SHANDON),附着在滑动玻璃上,进行迈格林瓦特盖姆萨(May-Grinwald-Gremsa)(MERCK)染色。在显微镜下将500个细胞分类成巨噬细胞、嗜酸性细胞,中性白细胞及淋巴细胞,调查其比例,乘以总细胞数,计算各细胞数。
2.结果
结果如图4所示。从图表明,本发明的化合物(I-963),明显地抑制通过诱发抗原引起的嗜酸性白细胞及中性白细胞数的增加。
试验例8 小白鼠T细胞株EL-4的细胞因子产生的抑制效果
在48孔板的各孔中加入将小白鼠T细胞株EL-4、2×105个浮游在0.2ml的1%牛胎儿血清加RPMI 1640培养基(添加碳酸氢钠2mM、青霉素50单位/ml、链霉素50μg/ml及2-巯基乙醇5×10-5M)的物质,在各孔中以各种浓度加入本发明的化合物,加入作为细胞的刺激剂的TPA,使最终浓度达10ng/ml,使各孔的最终容量为0.4ml。将本发明的各化合物溶解在DMSO中,用上述RPMI 1640培养基稀释、添加,使最终浓度达100ng/ml以下。将48孔板放在湿度100%、二氧化碳5%、空气95%的培养器中,在37℃下培养24小时,回收各孔的培养上清液。在各孔中用ELISA试剂盒(Amersham K.K.社制)测定放出在培养基中的细胞因子中的IL-2、IL-4、IL-5,作为细胞的产生细胞因子的指标。对照组使用不添加TPA(-TPA)。结果如表334所示。表334
化合物 | IC50(ng/ml) | ||
IL-2 | IL-4 | IL-5 | |
I-4 | >500 | 14 | 120 |
I-37 | >500 | 7 | 110 |
I-39 | 1300 | 7 | 130 |
I-70 | >2000 | 0.2 | 1000 |
I-73 | 500 | 20 | 15 |
I-83 | >10000 | 140 | 1000 |
I-128 | >10000 | 140 | 450 |
I-148 | >10000 | 100 | 11000 |
I-157 | >10000 | 170 | >10000 |
I-189 | >10000 | 100 | 10000 |
I-190 | >100 | 7 | 10 |
I-202 | >2000 | <20 | <20 |
I-209 | >200 | 14 | 12 |
I-213 | >1000 | 25 | 23 |
I-218 | >1000 | 4.8 | 30 |
I-220 | >1000 | 150 | 720 |
I-223 | 1000 | 16 | 45 |
I-226 | 880 | 17 | 300 |
I-228 | >1000 | 21 | 30 |
I-229 | >1000 | 42 | 80 |
I-230 | >1000 | 13 | 20 |
I-231 | >500 | 9.6 | 9.2 |
I-233 | >1000 | 12 | 3.8 |
I-237 | >100 | 17 | 100 |
I-238 | >1000 | 35 | >1000 |
I-239 | >1000 | 54 | 900 |
I-242 | >1000 | 100 | 880 |
I-243 | >500 | 63 | >550 |
I-279 | >1000 | 38 | 90 |
I-282 | >500 | <5 | 130 |
I-292 | >1000 | 72 | 600 |
I-296 | >1000 | 70 | 47 |
I-301 | 500 | <10 | 120 |
I-302 | >1000 | 25 | 280 |
I-305 | >1000 | 10 | 340 |
I-307 | >1000 | 52 | 23 |
I-309 | >500 | 29 | 10 |
I-318 | >1000 | 68 | 58 |
I-323 | >1000 | 230 | 24 |
I-368 | >1000 | 72 | 380 |
I-375 | >1000 | 200 | >1000 |
I-379 | >1000 | 88 | >1000 |
I-386 | >1000 | 68 | 40 |
I-387 | >1000 | 75 | 40 |
I-390 | >1000 | 200 | 160 |
I-392 | >1000 | 50 | >1000 |
I-395 | >1000 | 1-10 | >1000 |
I-403 | >1000 | 13 | >1000 |
I-720 | >500 | 6 | 110 |
制剂例1 片剂
本发明化合物 15mg
淀粉 15mg
乳糖 15mg
结晶性纤维素 19mg
聚乙烯醇 3mg
蒸馏水 30mg
硬脂酸钙 3mg
将硬脂酸钙以外的成分均匀地混合、破碎、造粒、干燥,作成适当大的颗粒剂。接着,添加硬脂酸钙、压缩成形,作成片剂。
产业上利用的可能性
从以上试验表明,本发明化合物显示了强的免疫抑制作用和/或抗过敏性作用。因此,本发明化合物及与本发明化合物具有相同作用的物质,作为选择性的IgE产生抑制剂、免疫抑制剂和/或抗过敏剂是非常有用的。
Claims (17)
1.选择性的IgE产生抑制剂,包括在从成熟B细胞分化成产生抗体细胞,到产生抗体的过程中,抑制IgE产生,而不抑制或微弱抑制同时产生的IgG、IgM和/或IgA产生的物质。
2.权利要求1所述的选择性的IgE产生抑制剂,其中,IgE产生抑制和IgG、IgM和/或IgA产生抑制的选择性是10000倍以上。
3.权利要求1所述的选择性的IgE产生抑制剂,其中,与不存在所述抑制剂的情况比较,在抑制50%的IgE产生的浓度的10000倍的浓度下也不抑制50%以上的IgG、IgM和/或IgA的产生。
4.权利要求1~3所述的选择性的IgE产生抑制剂,其中,在对于因变态反应原感染的哺乳动物给药时,用抑制或微弱抑制IgM、IgG和/或IgA产生的用量,与不给药时比较,可抑制90%以上的IgE产生。
5.权利要求1~4所述的选择性的IgE产生抑制剂,其抑制炎症性细胞向组织浸润。
6.权利要求5所述的选择性的IgE产生抑制剂,其中,炎症性细胞是嗜酸性白细胞和/或嗜中性白细胞。
7.用表(I)表示的化合物,其药学上可接受的盐、其水合物或其前体药物,〔式中,R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、也可具有取代基的低级烷基磺酰氧基、也可具有取代基的低级烷基亚硫酰基、硝基、氰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基、也可具有取代基的氨磺酰基或也可具有取代基的杂环、X是-O-、-CH2-、-NR14-(其中,R14是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或乙酰基)或-S(O)p-(其中,p是0~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,Y是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基;另外,R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R11、R12及R13、R11及-X-Y或R13及-X-Y一起地形成含有1个以上的O、S或NR15(其中,R15是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或也可具有取代基的芳基磺酰基)的,可具有取代基的5~6元环;但是,除去R6、R7、R8及R9中,1个以上是卤素,其它的是氢;R6、R7、R8及R9都是卤素;及R2~R13都是氢,卤素或氰基中的任何1种的情况;另外,R6、R7、R8及R9同时都是氢时,R1不是氢、氟、也可具有取代基的低级烷基及也可具有取代基的低级烷氧基或R2、R3、R4、R5及R12都是氢或者R13不是氢及卤素;进而,R6、R7、R8或R9的至少1个是氢以外的基团时,R1不是甲基及乙酰氧基、或R13不是氢、也可具有取代基的低级烷氧基羰基及也可具有取代基的氨基甲酰基、或者-X-Y不是甲氧基、另外,除去用式(I′)表示的化合物,(式中,R1′是氢或烃基、R13′是羟基或甲氧基)〕。
8.权利要求7所述的化合物,其药学上可接受的盐、其水合物或其前体药物,其中,R1是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、低级烷基磺酰基、甲酰基、也可具有取代基的氨基、低级烷基亚硫酰基、酰氧基、硝基、氰基、也可具有取代基的氨磺酰基或杂环、R2是氢、羟基、卤素、也可具有取代基的低级烷基或也可具有取代基的低级烷基磺酰氧基、R3是氢、羟基、卤素或也可具有取代基的低级烷氧基、R4是氢、也可具有取代基的低级烷基、卤素、也可具有取代基的低级烷氧基、硝基或也可具有取代基的氨基、R5是氢、也可具有取代基的低级烷氧基、低级烷氧基羰基或羧基、R6是氢、卤素、也可具有取代基的低级烷基、羧基、低级烷氧基羰基、硝基、甲酰基、氨基或低级烷基磺酰氧基、R7及R8分别独立地是氢、卤素、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、甲酰基或也可具有取代基的氨基、R9是氢、羟基、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、也可具有取代基的氨基甲酰基或也可具有取代基的氨基、R10是氢或低级烷氧基、R11是氢、卤素、也可具有取代基的低级烷基、羧基、低级烷氧基羰基、也可具有取代基的低级烷基磺酰氧基、甲酰基、硝基或氨基、R12是氢、R13是羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯氧基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰氧基、甲酰基、硝基或也可具有取代基的氨基、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烯基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基、R1及R2、R1及R4、R8及R9、R11及-X-Y或R13及-X-Y,一起地形成含有1个以上的O或NR15(R15与权利要求7时定义相同)的,可具有取代基的5~6元环。
9.具有免疫抑制作用的权利要求7或8所述的化合物,其药学上可接受的盐或其水合物。
10.药物组合物,包括权利要求7或8所述的化合物,其药学上可接受的盐、其水合物或其前体药物。
11.免疫抑制剂,包括权利要求7或8所述的化合物、其药学上可接受的盐、其水合物或其前体药物。
12.抗过敏剂,包括权利要求7或8所述的化合物、其药学上可接受的盐、其水合物或其前体药物。
13.免疫抑制剂,其含有用式(II″)表示的化合物、其药学上可接受的盐、其水合物或其前体药物,〔式中,R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧基羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、也可具有取代基的低级烷基磺酰氧基、也可具有取代基的低级烷基亚硫酰基、硝基、氰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基、也可具有取代基的氨磺酰基或也可具有取代基的杂环、X是-O-、-CH2-、-NR14-(其中,R14是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或乙酰基)或-S(O)P-(其中,p是O~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,Y是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧基羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基;另外,R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R11、R12及R13、R11及-X-Y或R13及-X-Y,一起地形成含有1个以上的O、S或NR15(其中,R15是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或也可具有取代基的芳基磺酰基)的,可具有取代基的5~6元环;但是,除去用式(I′)表示的化合物,其药学上可接受的盐,它们的水合物或它们的前体药物,(式中,R1′是氢或羟基、R13′是羟基或甲氧基)〕。
14.抗过敏剂,其含有用权利要求13所述的式(I″)表示的化合物,其药学上可接受的盐、其水合物或其前体药物。
15.用式(I_)表示的化合物或其药学上可接受的盐或它们的水合物的制备方法,
〔式中,R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11、R12及R13分别独立地是氢、羟基、卤素、羧基、也可具有取代基的低级烷基、也可具有取代基的低级烷氧基、也可具有取代基的低级烯基、也可具有取代基的低级烯氧基、也可具有取代基的低级烷硫基、也可具有取代基的低级烷氧基羰基、也可具有取代基的酰氧基、也可具有取代基的低级烷基磺酰基、也可具有取代基的低级烷基磺酰氧基、也可具有取代基的低级烷基亚硫酰基、硝基、氰基、甲酰基、也可具有取代基的氨基、也可具有取代基的氨基甲酰基、也可具有取代基的氨磺酰基或也可具有取代基的杂环、X是-O-、-CH2-、-NR14-(其中,R14是氢、也可具有取代基的低级烷基、也可具有取代基的低级烯基或乙酰基)或-S(O)p-(其中,p是0~2的整数)、Y是也可具有取代基的低级烷基、也可具有取代基的低级烯基、也可具有取代基的低级炔基、也可具有取代基的酰基、也可具有取代基的环烷基、也可具有取代基的环烯基、也可具有取代基的芳基或也可具有取代基的杂环、X是-CH2-时,Y是也可具有取代基的低级烷氧基、X是-O-或-NR14-时,Y是也可具有取代基的低级烷氧羰基、也可具有取代基的低级烷基磺酰基或也可具有取代基的芳基磺酰基;另外,R1及R4、R1及R2、R2及R3、R4及R5、R6及R7、R8及R9、R10及R11、R12及R13、R11及-X-Y或R13及-X-Y,一起地形成含有1个以上的O、S或NR15(其中,R15是也可具有取代基的低级烷基、也可具有取代基的低级烯基或也可具有取代基的芳基磺酰基)的,可具有取代基的5~6元环;但是,除去R6、R7、R8及R9中,1个以上是卤素,其它的是氢;R6、R7、R8及R9都是卤素;及R2~R13都是氢,卤素或氰基中的任何1种的情况;另外,R6、R7、R8及R9同时都是氢时,R1不是氢、氟、也可具有取代基的低级烷基及也可具有取代基的低级烷氧基或者R2、R3、R4、R5及R12都是氢、或者R13不是氢及卤素;进而,R6、R7、R8或R9中至少1个是氢以外的基团时,R1不是甲基及乙酰氧基、或者R13不是氢、也可具有取代基的低级烷氧基羰基及也可具有取代基的氨基甲酰基或者-X-Y不是甲氧基。〕,其特征是将用式(II)表示的化合物和用式(III):〔式(II)及式(III)中,R1~R13、X及Y与权利要求7的定义相同、A及Z一方是二羟基硼烷、二低级烷氧基硼烷、二低级烷基硼烷、或
另一方是卤素或-OSO2(CqF2q+1)(其中,q是0~4的整数))表示的化合物进行反应或者用式(II′):表示的化合物和用式(III′):(式(II′)及式(III′)中,R1~R13、X及Y与权利要求7时定义相同、A及Z与上述式(II)及(III)时定义相同)表示的化合物进行反应。
17.权利要求15所述的式(I_)表示的化合物或其药学上可接受的盐或其水合物的制备方法,其特征是将用式(IV′):(式中,R6~R9与权利要求7所述的式(I)时定义相同、A1及A2分别独立地与权利要求15所述的式(III)的A定义相同。但是,A2是具有比A1高的反应性或具有相同反应性的基团)表示的化合物和用权利要求16所述的式(VI)表示的化合物进行反应、接着,与用权利要求16所述的式(V)表示的化合物进行反应。
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- 1997-07-30 KR KR1019997000747A patent/KR100338855B1/ko not_active IP Right Cessation
- 1997-07-30 ES ES97933837T patent/ES2212119T3/es not_active Expired - Lifetime
- 1997-07-30 AT AT97933837T patent/ATE256092T1/de not_active IP Right Cessation
- 1997-07-30 DK DK97933837T patent/DK0933346T3/da active
- 1997-07-30 PL PL97331497A patent/PL331497A1/xx unknown
- 1997-07-30 CZ CZ99303A patent/CZ30399A3/cs unknown
- 1997-07-30 CA CA002261339A patent/CA2261339A1/en not_active Abandoned
- 1997-07-30 DE DE69726745T patent/DE69726745T2/de not_active Expired - Fee Related
- 1997-07-30 EP EP97933837A patent/EP0933346B1/en not_active Expired - Lifetime
- 1997-07-30 US US09/214,277 patent/US7101915B1/en not_active Expired - Fee Related
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- 1997-07-30 BR BR9710780A patent/BR9710780A/pt not_active IP Right Cessation
- 1997-07-30 PT PT97933837T patent/PT933346E/pt unknown
- 1997-07-30 WO PCT/JP1997/002635 patent/WO1998004508A1/ja active IP Right Grant
- 1997-07-30 AU AU37067/97A patent/AU729320B2/en not_active Ceased
- 1997-07-30 IL IL12819097A patent/IL128190A0/xx unknown
- 1997-07-30 CN CN97198341A patent/CN1232443A/zh active Pending
- 1997-07-31 TW TW086110933A patent/TW510895B/zh not_active IP Right Cessation
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- 2003-11-12 US US10/705,505 patent/US7074836B1/en not_active Expired - Fee Related
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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CN104447452A (zh) * | 2014-11-06 | 2015-03-25 | 广东工业大学 | 一种巯基功能化多芳基羧酸化合物的合成方法 |
CN104447452B (zh) * | 2014-11-06 | 2016-04-20 | 广东工业大学 | 一种巯基功能化多芳基羧酸化合物的合成方法 |
CN110396415A (zh) * | 2018-04-25 | 2019-11-01 | 北京八亿时空液晶科技股份有限公司 | 一种新型液晶垂直配向剂及其制备方法与应用 |
CN110396415B (zh) * | 2018-04-25 | 2021-01-26 | 北京八亿时空液晶科技股份有限公司 | 一种新型液晶垂直配向剂及其制备方法与应用 |
CN113214056A (zh) * | 2021-04-16 | 2021-08-06 | 子辰海洋医药科技(上海)有限公司 | 联苯类化合物和二萜类化合物及其制备方法与应用 |
CN113214056B (zh) * | 2021-04-16 | 2023-08-29 | 子辰海洋医药科技(上海)有限公司 | 联苯类化合物和二萜类化合物及其制备方法与应用 |
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PT933346E (pt) | 2004-03-31 |
CA2261339A1 (en) | 1998-02-05 |
WO1998004508A1 (en) | 1998-02-05 |
TW510895B (en) | 2002-11-21 |
EP0933346B1 (en) | 2003-12-10 |
KR100338855B1 (ko) | 2002-12-28 |
RU2200730C2 (ru) | 2003-03-20 |
AU729320B2 (en) | 2001-02-01 |
ATE256092T1 (de) | 2003-12-15 |
US20040127495A1 (en) | 2004-07-01 |
US7220783B2 (en) | 2007-05-22 |
EP0933346A4 (en) | 2000-12-06 |
US7101915B1 (en) | 2006-09-05 |
DK0933346T3 (da) | 2004-03-29 |
JP4008498B2 (ja) | 2007-11-14 |
EP0933346A1 (en) | 1999-08-04 |
KR20000029669A (ko) | 2000-05-25 |
NZ333688A (en) | 2001-06-29 |
DE69726745T2 (de) | 2004-09-30 |
NO315369B1 (no) | 2003-08-25 |
CZ30399A3 (cs) | 1999-07-14 |
IL128190A0 (en) | 1999-11-30 |
BR9710780A (pt) | 1999-08-17 |
PL331497A1 (en) | 1999-07-19 |
US7074836B1 (en) | 2006-07-11 |
ES2212119T3 (es) | 2004-07-16 |
DE69726745D1 (de) | 2004-01-22 |
NO990415D0 (no) | 1999-01-28 |
NO990415L (no) | 1999-03-26 |
AU3706797A (en) | 1998-02-20 |
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