CN1765900A - 含萘酰亚胺单元的螺噁嗪衍生物 - Google Patents
含萘酰亚胺单元的螺噁嗪衍生物 Download PDFInfo
- Publication number
- CN1765900A CN1765900A CN 200510030813 CN200510030813A CN1765900A CN 1765900 A CN1765900 A CN 1765900A CN 200510030813 CN200510030813 CN 200510030813 CN 200510030813 A CN200510030813 A CN 200510030813A CN 1765900 A CN1765900 A CN 1765900A
- Authority
- CN
- China
- Prior art keywords
- compound
- alkyl
- formula
- naph
- nitro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000003003 spiro group Chemical group 0.000 title description 8
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical group C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 title description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 150000002367 halogens Chemical class 0.000 claims abstract description 3
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 3
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 58
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 229960000890 hydrocortisone Drugs 0.000 claims description 12
- 125000005466 alkylenyl group Chemical group 0.000 claims description 4
- 125000002837 carbocyclic group Chemical group 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- ZTQSADJAYQOCDD-UHFFFAOYSA-N ginsenoside-Rd2 Natural products C1CC(C2(CCC3C(C)(C)C(OC4C(C(O)C(O)C(CO)O4)O)CCC3(C)C2CC2O)C)(C)C2C1C(C)(CCC=C(C)C)OC(C(C(O)C1O)O)OC1COC1OCC(O)C(O)C1O ZTQSADJAYQOCDD-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000005936 piperidyl group Chemical group 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract description 11
- -1 C1~C12 alkoxy Chemical group 0.000 abstract description 6
- 239000011232 storage material Substances 0.000 abstract description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- 125000004008 6 membered carbocyclic group Chemical group 0.000 abstract 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 241001597008 Nomeidae Species 0.000 abstract 1
- 230000002862 amidating effect Effects 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 230000001546 nitrifying effect Effects 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000000243 solution Substances 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 8
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 8
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- 229960000583 acetic acid Drugs 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000012362 glacial acetic acid Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000000862 absorption spectrum Methods 0.000 description 4
- 238000013375 chromatographic separation Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000002194 synthesizing effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000006396 nitration reaction Methods 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000005286 illumination Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000006277 sulfonation reaction Methods 0.000 description 2
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- DPDMMXDBJGCCQC-UHFFFAOYSA-N [Na].[Cl] Chemical compound [Na].[Cl] DPDMMXDBJGCCQC-UHFFFAOYSA-N 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- ZLWLTDZLUVBSRJ-UHFFFAOYSA-K chembl2360149 Chemical compound [Na+].[Na+].[Na+].O=C1C(N=NC=2C=CC(=CC=2)S([O-])(=O)=O)=C(C(=O)[O-])NN1C1=CC=C(S([O-])(=O)=O)C=C1 ZLWLTDZLUVBSRJ-UHFFFAOYSA-K 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000001455 metallic ions Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Images
Landscapes
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
Abstract
Description
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100308136A CN100430404C (zh) | 2005-10-28 | 2005-10-28 | 含萘酰亚胺单元的螺噁嗪衍生物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100308136A CN100430404C (zh) | 2005-10-28 | 2005-10-28 | 含萘酰亚胺单元的螺噁嗪衍生物 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1765900A true CN1765900A (zh) | 2006-05-03 |
CN100430404C CN100430404C (zh) | 2008-11-05 |
Family
ID=36742037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2005100308136A Active CN100430404C (zh) | 2005-10-28 | 2005-10-28 | 含萘酰亚胺单元的螺噁嗪衍生物 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100430404C (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109705648A (zh) * | 2018-12-25 | 2019-05-03 | 上海甘田光学材料有限公司 | 一种新型含氟萘酯类成膜助剂在变色涂料中的应用 |
CN109762000A (zh) * | 2019-02-12 | 2019-05-17 | 赤峰学院 | 基于1,8-萘酰亚胺单元的螺噁嗪类氢离子荧光探针化合物及其合成方法和应用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1446815A (zh) * | 2002-03-26 | 2003-10-08 | 中国科学院理化技术研究所 | 苯并吲哚啉螺萘并噁嗪化合物及其合成方法和用途 |
CN100434430C (zh) * | 2002-07-02 | 2008-11-19 | 中国科学院理化技术研究所 | 吲哚啉螺苯并噁嗪化合物及其合成方法和用途 |
CN1300145C (zh) * | 2004-05-31 | 2007-02-14 | 中国科学院理化技术研究所 | 吲哚啉螺菲并噁嗪化合物及其合成方法和用途 |
-
2005
- 2005-10-28 CN CNB2005100308136A patent/CN100430404C/zh active Active
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109705648A (zh) * | 2018-12-25 | 2019-05-03 | 上海甘田光学材料有限公司 | 一种新型含氟萘酯类成膜助剂在变色涂料中的应用 |
CN109762000A (zh) * | 2019-02-12 | 2019-05-17 | 赤峰学院 | 基于1,8-萘酰亚胺单元的螺噁嗪类氢离子荧光探针化合物及其合成方法和应用 |
CN109762000B (zh) * | 2019-02-12 | 2021-03-30 | 赤峰学院 | 基于1,8-萘酰亚胺单元的螺噁嗪类氢离子荧光探针化合物及其合成方法和应用 |
Also Published As
Publication number | Publication date |
---|---|
CN100430404C (zh) | 2008-11-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1239503C (zh) | 液晶苝-3,4:9,10-四羧酸二酰亚胺 | |
CN1222518C (zh) | 锌荧光探针 | |
CN1277821C (zh) | 并苯衍生物及其作为染料的用途 | |
CN1136288C (zh) | 可光交联的液晶染料 | |
CN1073081C (zh) | 萘酚衍生物及其制备方法 | |
CN1296371C (zh) | 光致变色双萘并吡喃化合物 | |
JP2013173726A (ja) | クマリン誘導体 | |
CN1765900A (zh) | 含萘酰亚胺单元的螺噁嗪衍生物 | |
CN1049232C (zh) | 一种具有双发色团的荧光染料及其制备方法 | |
CN1349522A (zh) | 2,2-二甲基-1,3-二氧杂环己烷中间体的盐及其制备方法 | |
CN1976909A (zh) | 新的异苯并嗪酮及其作为紫外光吸收剂的用途 | |
CN1194966C (zh) | 使用碳酸二甲酯的吲哚化合物的甲基化反应 | |
CN1827574A (zh) | 金丝桃素及其衍生物的化学合成方法 | |
CN100349869C (zh) | 含端炔基的菁染料及其合成方法 | |
CN1305861C (zh) | 光致变色嗪化合物和用于其制造的方法 | |
CN104892485A (zh) | 2-全氟烷基吲哚衍生物及其合成方法 | |
CN1255404C (zh) | 制备取代的咪唑并吡啶化合物的方法 | |
CN1634900A (zh) | 3-甲基-2-苯并噻唑啉酮腙及其盐酸盐的制备方法 | |
CN1869129A (zh) | 含香豆素的菁染料 | |
CN1320378C (zh) | 电子显示装置用过滤器 | |
CN1178919C (zh) | 用于制备三环化合物的中间体的合成方法及其中的中间体 | |
CN1170816C (zh) | N、n'-二取代苯胺基芳香二甲酰胺及其衍生物、制备方法和用途 | |
CN1148433C (zh) | 键合抗氧剂分子的光致变色螺恶嗪化合物及其制备方法和用途 | |
CN1869021A (zh) | 一种替加色罗的制备方法 | |
CN1284775C (zh) | 3-未取代-5-氨基-4-亚硝基吡唑化合物的制法以及2-肟基-3-氧代丙腈、3-亚肼基-2-肟基丙腈化合物和它们的制法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Suzhou Antina Photosensitive New Materials Co., Ltd. Assignor: East China University of Science and Technology Contract fulfillment period: 2009.5.1 to 2019.4.30 Contract record no.: 2009310000147 Denomination of invention: Spiro f derivatives containing a naphthalene imide unit Granted publication date: 20081105 License type: Exclusive license Record date: 2009.8.4 |
|
LIC | Patent licence contract for exploitation submitted for record |
Free format text: EXCLUSIVE LICENSE; TIME LIMIT OF IMPLEMENTING CONTACT: 2009.5.1 TO 2019.4.30; CHANGE OF CONTRACT Name of requester: SUZHOU ANTIAN SENSITIZATION NEW MATERIALS CO., LTD Effective date: 20090804 |
|
EC01 | Cancellation of recordation of patent licensing contract |
Assignee: Suzhou Antina Photosensitive New Materials Co., Ltd. Assignor: East China University of Science and Technology Contract record no.: 2009310000147 Date of cancellation: 20150428 |
|
LICC | Enforcement, change and cancellation of record of contracts on the licence for exploitation of a patent or utility model | ||
EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20060503 Assignee: Shanghai Gantian Optical Material Co., Ltd. Assignor: East China University of Science and Technology Contract record no.: 2015310000065 Denomination of invention: Spiro oxazone derivative containing naphthalimide unit Granted publication date: 20081105 License type: Exclusive License Record date: 20150526 |
|
LICC | Enforcement, change and cancellation of record of contracts on the licence for exploitation of a patent or utility model | ||
TR01 | Transfer of patent right |
Effective date of registration: 20180628 Address after: 201515 518 Jinhuan Road, Jinshan Town, Jinshan District, Shanghai Patentee after: Shanghai Gantian Optical Material Co., Ltd. Address before: 200237 No. 130, Meilong Road, Shanghai, Xuhui District Patentee before: East China University of Science and Technology |
|
TR01 | Transfer of patent right |