TW201838997A - Compounds as modulators of ror gamma - Google Patents

Compounds as modulators of ror gamma Download PDF

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TW201838997A
TW201838997A TW107126507A TW107126507A TW201838997A TW 201838997 A TW201838997 A TW 201838997A TW 107126507 A TW107126507 A TW 107126507A TW 107126507 A TW107126507 A TW 107126507A TW 201838997 A TW201838997 A TW 201838997A
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mmol
compound
pharmaceutically acceptable
acceptable salt
mixture
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TW107126507A
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班克伊喬安娜
理查 布魯奈特史蒂芬
柯林戴芬妮
歐文 休斯羅伯特
李翔
梁爽
西波里羅伯特
羅伯特 杜納麥可
吳立芬
張強
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德商百靈佳殷格翰國際股份有限公司
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Abstract

The present invention encompasses compounds of the formula (I) wherein the variables are defined herein which are suitable for the modulation of ROR[gamma] and the treatment of diseases related to the modulation of ROR[gamma]. The present invention also encompasses processes of making compounds of formula (I) and pharmaceutical preparations containing them.

Description

作為RORγ調節劑之化合物Compound as a RORγ modulator

本發明係關於調節RORγ活性之新穎化合物及其等作為藥劑之用途。The present invention relates to novel compounds for modulating RORy activity and their use as medicaments.

RORγ (與視網酸受體相關之孤兒受體γ) (亦稱作「RORγt」)係屬於類固醇激素受體超家族之轉錄因子(文獻回顧Jetten 2006. Adv. Dev Biol. 16 : 313-355.)。RORγ已被識別為T細胞分化及一組稱為Th17 細胞之T細胞分泌介白素17(IL-17)所需的轉錄因子(Ivanov, Cell 2006, 126, 1121-1133)。RORγ標靶治療於治療慢性發炎性疾病之用途的基本原理係基於Th17 細胞及細胞介素IL-17導致若干自體免疫疾病之發病機制之開始及進展之新證據，該等自體免疫疾病包含牛皮癬、關節黏連性脊椎炎、類風濕性關節炎、多發性硬化症及克羅恩氏病(Crohn's disease)(文獻回顧Miossec, Nature Drug Discovery 2012, 11, 763-776；亦參見Khan等人，Bioorganic & Medicinal Chemistry Letters 23 (2013), 532-536)。使用IL-17及其受體IL-17RA之中和抗體(Leonardi 2012, New England Journal of Medicine, 366, 1190-1199；Papp 2012, New England Journal of Medicine 366, 1181-1189)之現代臨床試驗在牛皮癬中之結果強調IL-17在此疾病之發病機制中的作用。因此，經由抑制RORγ衰減自活性Th17 T細胞之IL-17分泌可提供類似治療效益。RORγ (orphan receptor gamma associated with reticulum receptors) (also known as "RORγt") is a transcription factor of the steroid hormone receptor superfamily (reviewed by Jetten 2006. Adv. Dev Biol. 16 : 313-355 .). RORγ has been identified as a transcription factor required for T cell differentiation and a group of T cells called Th 17 cells to secrete interleukin 17 (IL-17) (Ivanov, Cell 2006, 126, 1121-1133). The rationale for the use of RORγ targets in the treatment of chronic inflammatory diseases is based on new evidence that Th 17 cells and interleukin IL-17 lead to the onset and progression of several autoimmune diseases, such autoimmune diseases. Contains psoriasis, joint adhesion spondylitis, rheumatoid arthritis, multiple sclerosis, and Crohn's disease (reviewed by Miossec, Nature Drug Discovery 2012, 11, 763-776; see also Khan et al. Human, Bioorganic & Medicinal Chemistry Letters 23 (2013), 532-536). Modern clinical trials using IL-17 and its receptor IL-17RA neutralizing antibody (Leonardi 2012, New England Journal of Medicine, 366, 1190-1199; Papp 2012, New England Journal of Medicine 366, 1181-1189) The results in psoriasis emphasize the role of IL-17 in the pathogenesis of this disease. Thus, by inhibiting the activity of RORγ attenuation from Th 17 T cell secretion of IL-17 may provide a therapeutic benefit similar.

本發明包括一種新類類別的雜芳族化合物及其製造及使用方法，該等化合物具有式(I)之一般結構，其中取代基係如本文所定義：(I) 此等化合物可用於治療自體免疫及過敏性疾病，其中其等對RORγ展示較好的調節效應。The present invention includes a novel class of heteroaromatic compounds having a general structure of formula (I) wherein the substituents are as defined herein, and methods of making and using the same. (I) These compounds are useful in the treatment of autoimmune and allergic diseases in which they exhibit a better regulatory effect on RORy.

所用定義及規約 本文未明確定義之術語具有熟習此項技術者根據全部揭示內容及作為整體之上下文所瞭解之含義。 如本文所使用，除非另有說明，否則採用下列定義： 前綴Cx-y 之用途(其中x及y各表示自然數)指示以直接聯繫規定及提及之鏈或環結構或鏈及環結構作為整體之組合可由最大值y及最小值x數量之碳原子組成。 一般言之，對於包括兩個或更多個子基團之基團而言，除非另有說明，否則最後命名之子基團係基團附接點，例如，取代基「芳基-C1-3 -烷基」意謂鍵結至C1-3 -烷基之芳基，前者鍵結至附接該取代基之核或基團。然而，若恰在第一命名之子基團前描述鍵，則該第一命名之子基團係基團附接點，例如，取代基「-S(O)n C1-6 烷基」意謂鍵結至S(O)n 基團之C1-6 -烷基，前者鍵結至附接該取代基之核或基團。 烷基表示可以直鏈(無分支)及分支鏈形式存在之單價、飽和烴鏈。若烷基係經取代，則該取代可彼此獨立地發生於(在各情況下經單取代或多取代)所有載氫碳原子上。 例如，術語「C1-5 烷基」包含例如H3 C-、H3 C-CH2 -、H3 C-CH2 -CH2 -、H3 C-CH(CH3 )-、H3 C-CH2 -CH2 -CH2 -、H3 C-CH2 -CH(CH3 )-、H3 C-CH(CH3 )-CH2 -、H3 C-C(CH3 )2 -、H3 C-CH2 -CH2 -CH2 -CH2 -、H3 C-CH2 -CH2 -CH(CH3 )-、H3 C-CH2 -CH(CH3 )-CH2 -、H3 C-CH(CH3 )-CH2 -CH2 -、H3 C-CH2 -C(CH3 )2 -、H3 C-C(CH3 )2 -CH2 -、H3 C-CH(CH3 )-CH(CH3 )-及H3 C-CH2 -CH(CH2 CH3 )-。 烷基之其他實例係甲基(Me；-CH3 )、乙基(Et；-CH2 CH3 )、1-丙基(正丙基；n-Pr；-CH2 CH2 CH3 )、2-丙基(i-Pr；異丙基；-CH(CH3 )2 )、1-丁基(正丁基；n-Bu；-CH2 CH2 CH2 CH3 )、2-甲基-1-丙基(異丁基；i-Bu；-CH2 CH(CH3 )2 )、2-丁基(第二丁基；sec-Bu；-CH(CH3 )CH2 CH3 )、2-甲基-2-丙基(第三丁基；t-Bu；-C(CH3 )3 )、1-戊基(正戊基；-CH2 CH2 CH2 CH2 CH3 )、2-戊基(-CH(CH3 )CH2 CH2 CH3 )、3-戊基(-CH(CH2 CH3 )2 )、3-甲基-1-丁基(異戊基；-CH2 CH2 CH(CH3 )2 )、2-甲基-2-丁基(-C(CH3 )2 CH2 CH3 )、3-甲基-2-丁基(-CH(CH3 )CH(CH3 )2 )、2,2-二甲基-1-丙基(新戊基；-CH2 C(CH3 )3 )、2-甲基-1-丁基(-CH2 CH(CH3 )CH2 CH3 )、1-己基(正己基；-CH2 CH2 CH2 CH2 CH2 CH3 )、2-己基(-CH(CH3 )CH2 CH2 CH2 CH3 )、3-己基(-CH(CH2 CH3 )(CH2 CH2 CH3 )) 、2-甲基-2-戊基(-C(CH3 )2 CH2 CH2 CH3 )、3-甲基-2-戊基(‑CH(CH3 )CH(CH3 )CH2 CH3 )、4-甲基-2-戊基(-CH(CH3 )CH2 CH(CH3 )2 ) 、3-甲基-3-戊基(-C(CH3 )(CH2 CH3 )2 )、2-甲基-3-戊基(-CH(CH2 CH3 )CH(CH3 )2 )、2,3-二甲基-2-丁基(-C(CH3 )2 CH(CH3 )2 )、3,3-二甲基-2-丁基(-CH(CH3 )C(CH3 )3 )、2,3-二甲基-1-丁基(-CH2 CH(CH3 )CH(CH3 )CH3 )、2,2-二甲基-1-丁基(-CH2 C(CH3 )2 CH2 CH3 )、3,3-二甲基-1-丁基(-CH2 CH2 C(CH3 )3 )、2-甲基-1-戊基(-CH2 CH(CH3 )CH2 CH2 CH3 )、3-甲基-1-戊基(-CH2 CH2 CH(CH3 )CH2 CH3 )、1-庚基(正庚基)、2-甲基-1-己基、3-甲基-1-己基、2,2-二甲基-1-戊基、2,3-二甲基-1-戊基、2,4-二甲基-1-戊基、3,3-二甲基-1-戊基、2,2,3-三甲基-1-丁基、3-乙基-1-戊基、1-辛基(正辛基)、1-壬基(正壬基)、1-癸基(正癸基)等。 關於無任何其他定義之術語丙基、丁基、戊基、己基、庚基、辛基、壬基、癸基等意謂具有相應碳原子數之飽和烴基，其中包含所有異構形式。 若烷基係其他(經組合之)基團(諸如例如，Cx-y 烷基胺基或Cx-y 烷氧基)之一部分時，則亦採用上文之烷基的定義。 不同於烷基，烯基(當單獨使用或組合使用時)由至少兩個碳原子組成，其中至少兩個相鄰碳原子係藉由C-C雙鍵連接在一起且碳原子僅可係C-C雙鍵之一部分。若在如上文中定義之具有至少兩個碳原子之烷基中，形式上移除相鄰碳原子上之兩個氫原子並使自由價飽和以形成第二鍵，從而形成相應的烯基。 烯基可視需要以對於雙鍵之順式或反式或E或Z定向存在。 不同於烷基，炔基(當單獨使用或組合使用時)由至少兩個碳原子組成，其中至少兩個相鄰碳原子係藉由C-C三鍵連接在一起。若在如上文中定義之具有至少兩個碳原子之烷基中，形式上移除相鄰碳原子上之各兩個氫原子並使自由價飽和以形成另外兩個鍵，從而形成相應的炔基。 鹵代烷基(鹵代烯基、鹵代炔基)(當單獨使用或組合使用時)係衍生自先前定義之烷基(烯基、炔基)，衍生方式為使該烴鏈之一個或多個氫原子彼此獨立地經鹵素原子(其可係相同或不同)置換。若鹵代烷基(鹵代烯基、鹵代炔基)欲經進一步取代，則該等取代可彼此獨立地發生於(在各情況下呈單取代或多取代之形式)所有載氫碳原子上。 鹵代烷基(鹵代烯基、鹵代炔基)之實例係-CF3 、-CHF2 、-CH2 F、-CF2 CF3 、-CHFCF3 、-CH2 CF3 、-CF2 CH3 、-CHFCH3 、-CF2 CF2 CF3 、-CF2 CH2 CH3 、-CF=CF2 、-CCl=CH2 、-CBr=CH2 、-C≡C-CF3 、-CHFCH2 CH3 、-CHFCH2 CF3 等。 鹵素係關於氟、氯、溴及/或碘原子。 術語「環烷基」(當單獨使用或組合使用時)係指非芳族3至12員(但較佳係3至6員)單環碳環基或非芳族6至10員稠合雙環、橋接雙環、螺槳烷或螺環碳環基。C3-12 環烷基可係飽和或部分飽和，且該碳環可藉由該環之任意原子附接，從而產生穩定結構。3至10員單環碳環之非限制性實例包含環丙基、環丁基、環戊基、環戊烯基、環己基、環己烯基、環庚基、環庚烯基及環己酮。6至10員稠合雙環碳環基之非限制性實例包含雙環[1.1.1]戊烷、雙環[3.3.0]辛烷、雙環[4.3.0]壬烷及雙環[4.4.0]癸基(十氫萘基)。6至10員橋接雙環碳環基之非限制性實例包含雙環[2.2.2]庚烷基、雙環[2.2.2]辛烷基及雙環[3.2.1]辛烷基。6至10員螺槳烷碳環基之非限制性實例包含(但不限於)[1.1.1.]螺槳烷、[3.3.3]螺槳烷及[3.3.1]螺槳烷。6至10員螺環碳環基之非限制性實例包含(但不限於)螺[3,3]庚烷基、螺[3,4]辛烷基及螺[4,4]庚烷基。 術語「雜環基」(當單獨使用或組合使用時)係指含有2至10個碳原子及1至4個選自NH、NR’、氧及硫(其中R’係C1-6 烷基)之雜原子環原子且包含穩定之非芳族4至8員單環雜環基或穩定之非芳族6至11員稠合雙環、橋接雙環或螺環雜環基的雜環系統。該雜環可係完全飽和或部分飽和。在一項實施例中，該雜環係C3-6 雜環，即，其含有3至6個環碳原子。非芳族單環雜環基之非限制性實例包含四氫呋喃基、氮雜環丁烷基、吡咯啶基、哌喃基、四氫哌喃基、二噁烷基、硫代嗎啉基、1,1-二側氧基-1.λ6 -硫代嗎啉基、嗎啉基、哌啶基、哌嗪基及氮呯基(azepinyl)。非芳族6至11員稠合雙環基之非限制性實例包含八氫吲哚基、八氫苯并呋喃基及八氫苯并噻吩基。非芳族6至11員橋接雙環基之非限制性實例包含2-氮雜雙環[2.2.1]庚烷基、3-氮雜雙環[3.1.0]己烷基及3-氮雜雙環[3.2.1]辛烷基。非芳族6至11員螺環雜環基之非限制性實例包含7-氮雜-螺[3,3]庚烷基、7-螺[3,4]辛烷基及7-氮雜-螺[3,4]辛烷基。硫及氮可視需要存在於所有可能之氧化階段(硫à亞碸-SO-、碸-SO2 -；氮àN-氧化物)中。 術語「芳基」(當單獨使用或組合使用時)係指含有自六至十四個碳環原子之芳族烴環(例如，C6-14 芳基，較佳係C6-10 芳基)。術語C6-14 芳基包含單環、稠合環及雙環，其中該等環中之至少一者係芳族環。C6-14 芳基之非限制性實例包含苯基、二氫茚基、茚基、苯并環丁烷基、二氫萘基、四氫萘基、萘基、苯并環庚烷基及苯并環庚烯基。 如本文使用，術語「雜芳基」(當單獨使用或組合使用時)係指含有2至10個碳原子及1至4個選自N、NH、NR’、O及S(其中R’係C1-6 烷基)之雜原子環原子且包含芳族5至6員單環雜芳基及芳族7至11員雜芳基雙環或稠合環(其中該等環中之至少一者係芳族環)的雜芳基環系統。5至6員單環雜芳基環之非限制性實例包含呋喃基、噁唑基、異噁唑基、噁二唑基、哌喃基、噻唑基、吡唑基、吡咯基、咪唑基、四唑基、三唑基、噻吩基、噻二唑基、吡啶基、嘧啶基、噠嗪基、吡嗪基、三嗪基及嘌呤基。7至11員雜芳基雙環或稠合環之非限制性實例包含苯并咪唑基、1,3-二氫苯并咪唑-2-酮、喹啉基、二氫-2H-喹啉基、異喹啉基、喹唑啉基、吲唑基、噻吩并[2,3-d]嘧啶基、吲哚基、異吲哚基、吲唑基、苯并三唑基、苯并呋喃基、苯并哌喃基、苯并間二氧雜環戊烯基、苯并噁唑基、苯并噻唑基、吡咯并[2,3-b]吡啶基及咪唑并[4,5-b]吡啶基。硫及氮可視需要存在於所有可能之氧化階段(硫à亞碸-SO-、碸-SO2 -；氮àN-氧化物)中。 本發明之化合物僅係熟習此項技術者所瞭解之彼等經考慮係化學穩定者。例如，具有「懸空價」或碳陰離子之化合物係非本文揭示之本發明之方法所涵蓋的化合物。 除非特別說明，否則在整個本說明書及隨附申請專利範圍中，所給化學式或名稱將包括互變異構物及所有立體、光學及幾何異構物(例如，鏡像異構物、非鏡像異構物、E/Z異構物等)及其外消旋物及呈不同比例之各別鏡像異構物之混合物、非鏡像異構物之混合物或前述形式中之任何形式之混合物，其中存在此類異構物及鏡像異構物及鹽(包含其醫藥上可接受之鹽)及其相應非溶劑化形式及與醫藥上可接受之溶劑(諸如水、乙醇及類似物)之溶劑化形式。 本發明之化合物亦包含其同位素標記形式。本發明組合之活性劑之同位素標記形式與該活性劑相同，但實際上，該活性劑之一個或多個原子已經被具有不同於通常在自然中發現之該原子之原子質量或質量數之原子質量或質量數的一個多個原子所置換。可容易購得並可根據完善建立之程序併入本發明組合之活性劑中之同位素的實例包含氫、碳、氮、氧、磷、氟及氯之同位素，例如，分別係2 H、3 H、13 C、14 C、15 N、18 O、17 O、31 P、32 P、35 S、18 F及36 Cl。本發明組合之活性劑、其前藥或含有上述同位素及/或其他原子之其他同位素中之一者或多者之醫藥上可接受之鹽亦視為在本發明範圍內。 本文使用之片語「醫藥上可接受」係指彼等在合理醫學判斷範圍內適用於與人類及動物之組織接觸而無過多毒性、刺激性、過敏性反應或其他問題或併發症，並符合合理的利益/風險比之化合物、材料、組合物及/或劑型。醫藥上可接受之鹽包含彼等衍生自醫藥上可接受之無機及有機酸及鹼者。合適之酸之實例包含鹽酸、氫溴酸、硫酸、硝酸、過氯酸、延胡索酸、順丁烯二酸、磷酸、乙醇酸、乳酸、柳酸、琥珀酸、甲苯-對-硫酸、酒石酸、乙酸、檸檬酸、甲磺酸、蟻酸、苯甲酸、丙二酸、萘-2-硫酸及苯磺酸。可將其他酸(諸如草酸)(雖然其等本身非醫藥上可接受)用於製備在獲得該等化合物及其醫藥上可接受之酸加成鹽中可用作中間物之鹽中。可以來自於金屬諸如鋁、鈣、鋰、鎂、鉀、鈉、鋅及類似物之陽離子形成其他醫藥上可接受之鹽(亦參見Pharmaceutical salts, Birge, S.M.等人，J. Pharm. Sci., (1977),66 , 1-19)。 本發明之醫藥上可接受之鹽可藉由習知化學方法自含有鹼性或酸性部分之親體化合物合成。通常，此類鹽可藉由使此等化合物之游離酸或鹼形式與足量適當鹼或酸在水或諸如乙醚、乙酸乙酯、乙醇、異丙醇或乙腈或其混合物之有機稀釋劑中反應來製備。 出於本發明目的，治療有效量意謂可消除疾病之症狀或緩解此等症狀，或延長經治療之患者之存活時間之的物質的量。本發明之實施例 本發明之一般實施例係關於下式(I)之化合物或其醫藥上可接受之鹽：(I) 其中： R1 係： –CN； –S(O)n R6 ；–S(O)n NR7 R8 ；–S(O)(NR9 )R6 ； –N(R9 )C(O)R6 ；–N(R9 )C(O)OR6 ；–N(R9 )S(O)n R6 ； –C(O)OR9 ； –C(O)NR7 R8 ；或–C(O)R9 ；或 R1 之R6 、R7 、R8 或R9 可環化於W上以形成環；及 R2 及R3 各獨立地係： (A) –H； (B)視需要經一個、兩個或三個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 ； c) –CN； d) –CF3 ； e) –鹵基； f) –C(O)OR9 ； g) –C(O)N(R9 )2 ； h) –S(O)n R9 ；及 i) –S(O)n NR7 R8 ；或 (C) C3-6 環烷基； (D) C3-6 雜環基；或 R2 及R3 係與附接其等之碳一起形成C3-6 碳環；或 R2 及R3 係與附接其等之碳一起形成C3-6 雜環；或 R2 或R3 可環化於W上以形成環； R4 係： (A) 視需要經一個、兩個或三個選自以下各物之基團取代之C1-6 烷基： a) C3-6 環烷基； b) C3-6 雜環基； c) –OR9 ； d) –CN； e) –S(O)n R9 ； f) –鹵基；及 g) –CF3 ；或 (B)視需要經一個、兩個或三個選自以下各物之基團取代之C3-12 環烷基： a) C1-6 烷基； b) –OR9 ； c) –CN； d) –S(O)n R9 ； e) –鹵基；及 f) –CF3 ；或 (C)各視需要經一個、兩個或三個選自以下各物之基團取代之芳基、雜芳基或雜環基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –S(O)n R9 ； f) –鹵基；及 g) –CF3 ； R5 係各視需要經一個、兩個或三個選自以下各物之基團取代之芳基、雜芳基、雜環基或C3-12 環烷基： (A)各視需要經一個、兩個或三個選自以下各物之基團取代之C1-6 烷基、C3-6 環烷基或C3-6 雜環基： a) C3-6 環烷基； b) C3-6 雜環基； c) –OR9 ； d) –CN； e) –S(O)n NR7 R8 ； f) –S(O)n R9 ； g) –鹵基；及 h) –CF3 ；或 (B) –OR9 ； (C) –CN； (D) –CF3 ； (E) –鹵基； (F) –S(O)n NR7 R8 ； (G) –S(O)n R9 ；及 (H) –NR7 R8 ； W係各視需要經一個或兩個選自以下各物之基團取代之芳基、雜芳基、雜環基、C3-12 環烷基或炔基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ； f) –鹵基； g) –NR7 R8 ； h) –C(O)OR9 ；及 i) –C(O)N(R9 )2 ；R6 係選自： (A) –OH； (B)視需要經一個或兩個選自以下各物之基團取代之C1-6 烷基： a) C3-6 環烷基； b) –OR9 ； c) –CN； d) –CF3 ；及 e) –鹵基； (C) C3-6 環烷基；及 (D) –CF3 ； R7 及R8 係獨立地選自： (A) –H； (B)視需要經一個或兩個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 ； c) –CN； d) –鹵基；及 (C) C3-6 環烷基；或 R7 及R8 連同鍵結其等之氮一起形成具有3至6個碳原子之飽和環，其中該飽和環中之一個碳原子可視需要經–O–、–NR9 –或–S(O)n –置換； R9 係選自： (A) –H； (B)視需要經一個或兩個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 ； c) –CN； d) –CF3 ；及 e) –鹵基；或 (C) C3-6 環烷基；及 n係0、1或2。 各種取代基定義內之額外子實施例包含以下：R1 基團實施例 (1) R1 係： –CN； –S(O)n R6 ；–S(O)n NR7 R8 ； –N(H)S(O)n R6 ；或 –S(O)(NH)R6 ；及 其中： R6 係： (A)視需要經一個或兩個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 ；及 c) –CN；或 (B) C3-6 環烷基； R7 及R8 各獨立地係： (A) –H；或 (B) C1-3 烷基；及 R9 係選自： (A) –H； (B) C1-3 烷基；或 (C) C3-6 環烷基；及 n係1或2。 (2) R1 係： -S(O)n R6 ； -S(O)n NR7 R8 ；或 -S(O)(NH)R6 ；及 其中： R6 係： (A) 視需要經一個或兩個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 ；及 c) –CN；或 (B) C3-6 環烷基； R7 及R8 各獨立地係： (A) –H；或 (B) C1-3 烷基；及 R9 係選自： (A) –H； (B) C1-3 烷基；或 (C) C3-6 環烷基；及 n係1或2。 (3) R1 係–S(O)n R6 、–S(O)n NR7 R8 或–S(O)(NH)R6 ；及 R6 係C1-3 烷基；及 R7 及R8 各獨立地係： (A) –H；或 (B) C1-3 烷基；及 n係2。R2 及 R3 基團實施例 (1) R2 及R3 係各獨立地選自： (A) –H； (B)視需要經一個、兩個或三個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 ；或 c) –鹵基；及 R2 及R3 係與附接其等之碳一起形成C3-6 碳環；或 R2 及R3 係與附接其等之碳一起形成C3-6 雜環；及 R9 係選自： (A) –H；及 (B) C1-3 烷基。 (2) R2 及R3 係各獨立地選自： (A) –H；及 (B) C1-3 烷基； (3) R2 及R3 係H。R4 基團實施例 (1) R4 係： (A)視需要經一個、兩個或三個選自以下各物之基團取代之C1-6 烷基： a) C3-6 環烷基； b) 4、5或6員雜環基； c) –OR9 ； d) –CN； e) –鹵基；及 f) –CF3 ；或 (B)視需要經一個、兩個或三個選自以下各物之基團取代之C3-6 環烷基： a) C1-6 烷基； b) –OR9 ； c) –CN； d) –鹵基；及 e) –CF3 ；及 其中該C3-6 環烷基中之一個碳可視需要經–O–置換； (C)苯基；或 (D) 4、5或6員雜環基；及 R9 係選自： (A) –H；及 (B) C1-3 烷基。 (2) R4 係： (A)視需要經一個或兩個選自以下各物之基團取代之C1-6 烷基： a) C3-6 環烷基； b) 4、5或6員雜環基； c) –OR9 ； d) –CN； e) –鹵基；及 f) –CF3 ；或 (B)視需要經一個、兩個或三個選自以下各物之基團取代之C3-6 環烷基： a) C1-6 烷基； b) –OR9 ； c) –CN； d) –鹵基；及 e) –CF3 ；或(C)苯基；或 (D) 4、5或6員雜環基；及 R9 係C1-3 烷基。 (3) R4 係： (A)視需要經一個或兩個選自C3-6 環烷基、鹵基、–CF3 及C1-3 烷氧基之基團取代之C1-6 烷基；或 (B)視需要經一個或兩個選自C1-6 烷基、–CF3 及鹵基之基團取代之C3-6 環烷基；或 (C) 5員雜環基。R5 基團實施例 (1) R5 係各視需要經一個、兩個或三個選自以下各物之基團取代的芳基、雜芳基或雜環基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ； f) –鹵基；及 g) –NR7 R8 ；及 R7 、R8 及R9 係各獨立地選自： (A) –H；及 (B) C1-3 烷基。 (2) R5 係： (A)視需要經一個、兩個或三個選自以下各物之基團取代之苯基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ；及 f) –鹵基；或 (B)視需要經一個、兩個或三個選自以下各物之基團取代之5或6員雜芳基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ； f) –鹵基；及 g) –NR7 R8 ；及 R7 、R8 及R9 係各獨立地選自： (A) –H；及 (B) C1-3 烷基。 (3) R5 係各視需要經一個、兩個或三個選自以下各物之基團取代之吡啶基或嘧啶基：a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CF3 ；及 e) –NR7 R8 ；及 R7 及R8 係各獨立地選自： (A) –H； (B) C1-3 烷基；及 R9 係C1-3 烷基。 (4) R5 係視需要經一個或兩個選自以下各物之基團取代之嘧啶基：a) C1-3 烷基； b) C3-5 環烷基； c) C1-3 烷氧基；及 d) –CF3 。W 基團實施例 (1) W係各視需要經一個或兩個選自以下各物之基團取代之苯基、吡啶基、嘧啶基、哌啶基、哌嗪基、吡嗪基或C3-12 環烷基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ； f) –鹵基； g) –NR7 R8 ； h) –C(O)OR9 ；及 i) –C(O)N(R9 )2 ；R7 、R8 及R9 係各選自： (A) –H；及 (B) C1-3 烷基。 (2) W係苯基、吡啶基、嘧啶基或哌啶基。 額外實施例包含上文R1 、R2 、R3 、R4 、R5 、R6 及W之子實施例之任何可能的組合。式 (I) 之額外子屬實施例 上式(I)之化合物之額外子屬實施例包含： (1)如上述式(I)之化合物或其醫藥上可接受之鹽，其中： R1 係： –S(O)nR6 ； –S(O)nNR7 R8 ；或 –S(O)(NH)R6 ； R2 及R3 係各獨立地選自： (A) –H；及 (B) C1-3 烷基； R4 係： (A)視需要經一個或兩個選自以下各物之基團取代之C1-6 烷基： a) C3-6 環烷基； b) 4、5或6員雜環基； c) –OR9 ； d) –CN； e) –鹵基；及 f) –CF3 ； (B)視需要經一個、兩個或三個選自以下各物之基團取代之C3-6 環烷基： a) C1-6 烷基； b) –OR9 ； c) –CN； d) –鹵基；及 e) –CF3 ；(C)苯基；或 (D) 5或6員雜環基； R5 係： (A)視需要經一個或兩個選自以下各物之基團取代之苯基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ；及 f) –鹵基；或 (B)各視需要經一個、兩個或三個選自以下各物之基團取代之吡啶基或嘧啶基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ； f) –鹵基；及 g) –NR7 R8 ；及 W係各視需要經一個或兩個選自以下各物之基團取代之苯基、吡啶基、嘧啶基、哌啶基或C3-12 環烷基： a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CN； e) –CF3 ； f) –鹵基； g) –NR7 R8 ； h) –C(O)OR9 ；及 i) –C(O)N(R9 )2 ；R6 係： (A)視需要經一個或兩個選自以下各物之基團取代之C1-3 烷基： a) C3-6 環烷基； b) –OR9 及 b) –CN；或 (B) C3-6 環烷基； R7 、R8 及R9 各獨立地係： (A) –H；或 (B) C1-3 烷基；及 n係2。 (2)如上述之式(I)之化合物或其醫藥上可接受之鹽，其中： R1 係–S(O)n R6 或–S(O)n NR7 R8 ；及 R2 及R3 係H； R4 係： (A)視需要經一個或兩個選自C3-6 環烷基、–CF3 及C1-3 烷氧基之基團取代之C1-6 烷基；或 (B)視需要經一個或兩個選自C1-6 烷基、–CN及鹵基之基團取代之C3-6 環烷基；或 (C) 5員雜環基； R5 係視需要經一個、兩個或三個選自以下各物之基團取代之嘧啶基：a) C1-6 烷基； b) C3-6 環烷基； c) –OR9 ； d) –CF3 ；及 e) –NR7 R8 ；W係苯基、吡啶基、嘧啶基或哌啶基； R6 係C1-3 烷基； R7 、R8 、R9 各獨立地係： (A) –H；或 (B) C1-3 烷基；及 n係2。 (3)如緊接上文在(2)中描述之式(I)之化合物或其醫藥上可接受之鹽，其中： R5 係視需要經一個或兩個選自以下各物之基團取代之嘧啶基：a) C1-3 烷基； b) C3-5 環烷基；及 c) C1-3 烷氧基；及 W係苯基、吡啶基、嘧啶基或哌啶基。 本發明範圍內之特定化合物包含下表I中之化合物或其醫藥上可接受之鹽： 表I 表I亦提供所有經製備之化合物之物理化學資料(即，HPLC滯留時間及質譜資料)。在下文合成實例部分中定義HPLC方法。 本發明進一步係關於式(I)之化合物與無機或有機酸或鹼之醫藥上可接受的鹽。 在另一態樣中，本發明係關於式(I)之化合物–或其醫藥上可接受之鹽–作為藥劑。 在另一態樣中，本發明係關於式(I)之化合物–或其醫藥上可接受之鹽–用於治療患者之方法中。 在另一態樣中，本發明係關於式(I)之化合物–或其醫藥上可接受之鹽–用於治療自體免疫疾病及過敏性疾病。 在另一態樣中，本發明係關於式(I)之化合物–或其醫藥上可接受之鹽的用途–用於製備治療自體免疫疾病及過敏性疾病之醫藥組合物。 在另一態樣中，本發明係關於一種用於治療自體免疫疾病及過敏性疾病之方法，其包括向患者投與治療有效量之式(I)之化合物–或一種其醫藥上可接受之鹽。 在另一態樣中，本發明係關於一種醫藥組合物，其含有作為活性物質之一種或多種式(I)之化合物–或其醫藥上可接受之鹽–視需要組合習知賦形劑及/或載劑。 可使用下文描述之一般合成方法製造式(I)之化合物，該等方法亦構成本發明之一部分。一般合成方法 可藉由合成方法、合成實例、一般技術者已知的方法及化學文獻資料中記錄之方法製備本發明之化合物。在下文描述之合成方法及實例中，取代基R1 、R2 、R3 、R4 、R5 及W應具有前文中對式I之化合物之詳細描述中所定義的含義。本文描述之此等方法旨在作為說明及用於實施本發明而非限制其標的、所主張之化合物及實例的範圍。在未描述初始化合物之製備之情況下，其等可購買獲得、可以類似本文描述之化合物或方法製備或描述於化學文獻資料中。除非另有說明，否則一般技術者可容易選擇溶劑、溫度、壓力及其他反應條件。 式R1 -W-C(R2 )(R3 )-NH2 之胺中間物可購買獲得；或可根據US 7,879,873及WO 2011/049917中描述之一般程序或參考文獻製備；或可藉由一般技術者使用化學文獻資料中描述之方法製備。 可根據流程圖I自中間物A’製備式(I)之化合物。 流程圖I如流程圖I中繪示，式A’之合適之嘧啶(其中G係NH2 ，X係適用於鈀媒介交叉偶合反應之基團(例如，I、Br、Cl或OSO2 CF3 )，及Y係合適之離去基(例如，Cl))可與式R4 NH2 之合適之胺或胺鹽(例如，鹽酸鹽)諸如異丙基胺在合適之鹼(例如，i-Pr2 EtN或Et3 N)之存在下於合適之溶劑(例如，正丁醇)中並在合適之反應條件(諸如合適之溫度(例如，約120℃))下反應以提供式B’之化合物。或者，式A’之該嘧啶(其中G係NH2 之合適之合成前驅物(例如，硝基))可與式R4 NH2 之合適之胺或胺鹽(例如，鹽酸鹽)諸如1-甲基環丙胺在合適之試劑及溶劑(例如，分別係i-Pr2 EtN及THF)之存在下於合適之反應條件(諸如合適之溫度(例如，約-78℃至約25℃))下反應以提供中間物，該中間物可在與合適之試劑(例如，NO2 基團可使用諸如SnCl2 之合適之試劑還原)進一步反應後轉化為式B’之化合物。熟習此項技術者對用於上述反應之式R4 NH2 之合適之胺及式A’之嘧啶之選擇可基於諸如該胺及該嘧啶之空間及電子性質之準則。式B’之二胺基嘧啶可與合適之試劑(諸如氯-側氧基-乙酸乙酯)在合適之溶劑(例如，丙酮)中並在合適之鹼(例如，K2 CO3 )的存在下反應以提供式C’之化合物。式C’之二羰基化合物可與合適之脫氯化氫試劑(諸如草醯氯)在合適之添加劑(例如，催化量之DMF)之存在下於合適之溶劑(例如，CH2 Cl2 )中，並在合適之反應條件(諸如適當之溫度(例如，約周圍溫度))下反應以提供式D’之化合物。式D’之氯-蝶啶酮可與式R1 -W-C(R2 )(R3 )-NH2 之合適之胺或胺鹽諸如4-乙烷磺醯基芐胺在合適之鹼(例如，Et3 N)之存在下於合適之溶劑(例如，THF)中並在合適之反應條件(諸如適當之溫度(例如，約周圍溫度))下反應以產生式E’之化合物。式E’之嘧啶可與合適之交叉偶合配偶體(例如，酸)及合適之鹼(例如，K3 PO4 )在合適之溶劑(例如，1,4-二噁烷)中，在合適之交叉偶合觸媒(例如，Pd(dppf)Cl2 )之存在下，在合適之反應條件(諸如合適之氣氛(例如，氬)及合適之溫度(例如，約100℃))下加熱以提供式(I)之化合物。合成實例 下文中提供展示本發明化合物之製法的非限制性實例。最佳反應條件及反應時間可視所用之特定試劑而變化。除非另有說明，否則一般技術者可容易選擇溶劑、溫度、壓力及其他反應條件。合成實例部分中提供特定程序。中間物及產物可藉由在矽膠上之層析法，再結晶作用及/或逆相HPLC(RHPLC)純化。可藉由使用掌性HPLC離析外消旋產物來獲得離散之鏡像異構物。RHPLC純化方法使用含於含有0.1%蟻酸或0.1% TFA之水中之0-100%之乙腈並使用下列管柱中之一者： a) Waters Sunfire OBD C18 5 μM 30x150 mm管柱 b) Waters XBridge OBD C18 5 μM 30x150 mm管柱 c) Waters ODB C8 5 μM 19x150 mm管柱 d) Waters Atlantis ODB C18 5 μM 19x50 mm管柱 e) Waters Atlantis T3 OBD 5 μM 30x100 mm管柱 f) Phenomenex Gemini Axia C18 5 μM 30x100 mm管柱 HPLC方法： 分析性LC/MS分析方法A： 管柱：Waters BEH 2.1x50mm C18 1.7um管柱 梯度： 分析性LC/MS分析方法B： 管柱：Waters BEH 2.1x50mm C18 1.7um管柱 梯度： 合成實例中所用之縮寫列表： 方法 1 ： 中間物 A 之合成 向A-1 (3.00 g，18.18 mmol)在正丁醇(10 mL)中之攪拌懸浮液中添加A-2 (10.80 g，18.18 mmol)，接著添加DIEA (6.46 mL，36.58 mmol)。在120℃下攪拌該混合物17 h。使該反應冷卻至rt並藉由添加飽和水性NH4 Cl溶液中止。然後用EtOAc稀釋該反應。分離有機層並用水清洗，接著用鹽水清洗。乾燥(Na2 SO4 )有機層，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生A-3 。 向A-3 (1.00 g，5.00 mmol)在丙酮(100 mL)中之攪拌懸浮液中添加草醯氯乙酯(0.88 g，6.43 mmol)，接著添加K2 CO3 (1.85g，13.39 mmol)。在rt下攪拌該混合物18 h並分離固體沉澱以產生A-4 。 向A-4 (1.14 g，5.00 mmol)在CH2 Cl2 (250 mL)中之攪拌懸浮液中添加草醯氯(1 mL)，接著添加5滴DMF。在rt下攪拌該混合物5 h。然後於減壓下濃縮該混合物以產生A-5 。 向A-5 (0.1 g，0.39 mmol)在THF (4 mL)中之攪拌懸浮液中添加TEA (0.16 mL，1.16 mmol) (或DIEA)，接著添加AG (91 mg，0.38 mmol)。容許在rt下攪拌該反應18 h。藉由添加飽和水性NH4 Cl溶液中止該反應並以EtOAc萃取有機物。以水及鹽水清洗有機層，乾燥(Na2 SO4 )，傾析並於真空下濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生中間物 A 。MS (ES+)： m/z 423.0 [M+H]+ 。方法 2 ： 中間物 B 之合成 在-78℃時，向B-1 (1.80 g，9.30 mmol)及B-2 (1.00 g，9.30 mmol)在THF (10 mL)中之攪拌懸浮液中添加DIEA (3.29 mL，18.59 mmol)並讓該反應緩慢升溫至25℃。於減壓下移除揮發物並將粗製物再溶解於EtOAc中及用H2 O清洗。分離有機層並用H2 O清洗兩次以上。用鹽水清洗有機層，乾燥(Na2 SO4 )，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生B-3 。 向B-3 (1.78 g，7.79 mmol)在EtOH (50 mL)中之溶液中添加SnCl2 (1.48 g，7.79 mmol)並加熱至回流，保持4 h。讓該反應冷卻至rt，然後傾倒於冰上。以1N NaOH(aq) 處理該溶液以使pH達到~9，然後濾過矽藻土墊。分離有機相並先以H2 O清洗後以鹽水清洗。乾燥(Na2 SO4 )有機層，傾析並濃縮。藉由SiO2 急驟層析法純化粗製產物以產生B-4 。 作為將硝基嘧啶還原為相應之胺基嘧啶的替代程序，已將下列一般程序用於類似中間物：向硝基嘧啶在EtOH中之溶液中添加觸媒RaNi。抽空反應容器並以N2 (g)純化，然後抽空並以H2 (g)填充。在H2 (g)氣氛下維持該反應15 h。抽空該容器並以N2 (g)吹掃。使該反應濾過矽藻土墊以移除Ni觸媒並濃縮濾液。藉由SiO2 急驟層析法純化所得殘餘物以提供相應的胺基嘧啶。 向B-4 (0.40 g，2.01 mmol)在丙酮(10 mL)中之攪拌溶液中添加K2 CO3 (0.70 g，5.06 mmol)，接著添加草醯氯乙酯(0.27 mL，2.43 mmol)。在rt下攪拌該反應24 h。然後過濾該反應，再溶解於H2 O中並用EtOAc萃取。分離水相並用EtOAc再萃取兩次。合併有機相，乾燥(Na2 SO4 )，傾析並濃縮以產生B-5 。 向B-5 (0.70 g，2.77 mmol)在CH2 Cl2 (50 mL)中之溶液中添加草醯氯(0.47 mL，5.54 mmol)，接著添加5滴DMF。容許在rt下攪拌該反應18 h。於真空中移除揮發物。將粗製物再溶解於DCM中並倒入H2 O中。分離有機層，用鹽水清洗，乾燥(Na2 SO4 )，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生B-6 。 向B-6 (0.83 g，3.06 mmol)在THF (10 mL)中之攪拌溶液中添加DIEA (1.07 mL，6.12 mmol)，接著添加AF (0.72 g，3.06 mmol)。在rt下攪拌該反應18 h。於真空中移除揮發物，使粗製殘餘物再懸浮於DCM中並倒入H2 O中。分離水相並用DCM再萃取兩次。合併有機層，用鹽水清洗，乾燥(Na2 SO4 )，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生中間物 B 。MS (ES+)：m/z 434.1 [M+H]+ 。 以類似方式製備下列中間物： (注：如方法34中之描述，可分離自A-3 (方法1)及B-4 (方法2)與草醯氯乙酯之反應所產生之草胺酸乙酯中間物並在合適之溫度(例如，130℃)下與合適之鹼(諸如TEA)在合適之溶劑(諸如EtOH)中加熱以分別提供相應的中間物A-4及B-5)。 方法 3 ： 中間物 AB 之合成 向AB-1 (300 mg，1.29 mmol)在無水MeOH (15 mL)中之溶液中添加NaOMe (208 mg，3.86 mmol)。在rt下攪拌該混合物1 h。過濾該溶液並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生中間物 AB 。MS (ES+)：m/z 230.8 [M+H]+ 。方法 4 ： 中間物 AC 之合成 向AC-1 (320 mg，2.07 mmol)、2,4,6-三甲基-1,3,5,2,4,6-三氧雜三硼烷(520 mg，4.14 mmol)及aq Na2 CO3 (2M，3.1 mL，6.21 mmol)在二噁烷(10 mL)中之溶液中添加二氯鈀4-二第三丁基磷基-N,N-二甲基苯胺(73 mg，0.10 mmol)。在微波反應器中將該混合物加熱至130℃並保持40 min。用MeOH (5 mL)稀釋該混合物，過濾並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AC-2 。 在-10℃時向AC-2 (363 mg，2.71 mmol)在EtOH (10 mL)中之溶液中添加Br2 (432 mg，2.71 mmol)。在rt下攪拌該反應混合物18 h。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生中間物 AC 。MS (ES+)：m/z 214.3 [M+H]+ 。方法 5 ： 中間物 AD 之合成 在16℃時攪拌AD-1 (100.0 g，0.70 mol)、乙酸甲脒(146 g，1.4 mol)及NaOMe (266.0 g，4.9 mol)在MeOH (2 L)中之混合物2天。用乙酸將該反應混合物中和至pH 7並過濾。於減壓下濃縮濾液並藉由SiO2 急驟層析法純化粗製產物以產生AD- 2 。 在0℃時向AD-2 (66.0 g，0.48 mol)及TEA (145.1 g，1.44 mol)在DCM (1.5 L)中之攪拌溶液中滴加Tf2 O (164.2 g，0.58 mol)在DCM (500 mL)中之溶液並攪拌3 h。藉由添加H2 O (200 mL)中止該反應混合物並用DCM (3 x 500 mL)萃取。用飽和aq NaHCO3 清洗合併之有機相，乾燥(Na2 SO4 )，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生AD-3 。 在回流時在N2 氣氛下攪拌AD-3 (17.0 g，0.06 mol)、乙烯基酸頻哪醇酯(29.3 g，0.09 mol)、K2 CO3 (26.3 g，0.19 mol)、Ag2 O (1.7 g，10重量%)及Pd(dppf)Cl2 (1.7 g，10重量%)在無水THF (400 mL)中之混合物18 h。使該混合物冷卻至rt並過濾。於減壓下濃縮濾液並藉由SiO2 急驟層析法純化所得殘餘物以產生AD-4 。 在H2 氣氛下攪拌AD-4 (27.3 g，0.28 mol)及RaNi (30.0 g，10重量%)在EtOH (500 mL)中之混合物16 h。用N2 吹掃容器並過濾內容物。於減壓下濃縮濾液並直接使用所得AD-5 (19.6 g)。 在-10℃時向AD-5 (19.6 g，0.13 mol)在EtOH (300 mL)中之攪拌溶液中添加Br2 (52.9 g，0.33 mol)。添加後，在rt下攪拌該混合物30 min。藉由添加10% Na2 S2 O3(aq) 溶液中止反應混合物並藉由添加10% Na2 CO3(aq) 溶液鹼化以調整至~pH 8。用EtOAc (3 x 200 mL)萃取該混合物。合併有機層，乾燥(Na2 SO4 )，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生中間物 AD 。MS (ES+)：m/z 228.9 [M+H]+ 。方法 6 ： 中間物 AE 之合成 向AC-1 (2.50 g，16.17 mmol)、環丙基酸(4.17 g，48.51 mmol)及Na2 CO3 (aq) (2M，24.26 mL，48.51 mmol)在二噁烷(30 mL)中之溶液中添加雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (572.5 mg，0.81 mmol)。密封容器並將其加熱至130℃並保持2 h。使該容器冷卻至rt，用MeOH稀釋並過濾。濃縮濾液並藉由SiO2 急驟層析法純化以產生AE-1 。 在-10℃時向AE-1 (660 mg，4.12 mmol)在EtOH (15 mL)中之溶液中添加Br2 (658 mg，4.12 mmol)。在rt下攪拌該反應3 h。添加NH3 之MeOH溶液(2N，1 mL)以中和。濃縮該混合物並藉由SiO2 急驟層析法純化以產生中間物 AE 。MS (ES+)： m/z 240.9 [M+H]+ 。方法 7 ： 中間物 AF 之合成 在80℃時，在密閉容器中攪拌AF-1 (100 g，561 mmol)、EtI (131 g，842 mmol)及TBAB (18 g，56 mmol)在H2 O (200 mL)、丙酮(150 mL)及甲苯(150 mL)中之混合物18 h。使該混合物分配在H2 O與EtOAc之間。乾燥有機層並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AF-2 。 使AF-2 (200 g，1.09 mol)、NBS (425.02 g，2.39 mol)及AIBN (17.82 g，108.54 mmol)在CCl4 (1.40 L)中之混合物回流18 h。使該混合物分配在H2 O與DCM之間。乾燥(Na2 SO4 )有機層，傾析並濃縮以產生AF-3 。 在0℃時向AF- 3 (333 g，974 mmol)及DIEA (129 g，1 mol)在ACN (500 mL)中之溶液中滴加在ACN (150 mL)中之AF-4 (138 g，1 mol)。攪拌該混合物5 h，隨後濃縮。自MeOH結晶所得殘餘物以產生AF-5 。 在-78℃時將AF-5 (50 g，190 mmol)在MeOH (200 mL)中之溶液添加至NH3 之MeOH溶液(2N，800 mL)中。在rt下攪拌該反應混合物18 h，隨後濃縮。自EtOAc結晶所得殘餘物以提供AF-6 。 在rt下攪拌AF-6 (50 g，250 mmol)在HCl之MeOH溶液(1N，250 mL)中之溶液12 h，隨後濃縮以產生呈HCl鹽之中間物 A F 。MS (ES+)：m/z 200.4 [M+H]+ 。方法 8 ： 中間物 AG 之合成 在N2 下，在rt時攪拌AG-1 (8.0 g，43.96 mmol)、K2 CO3 (7.88 g，57.1 mmol)及乙硫醇鈉(4.06 g，48.3 mmol)在NMP (60.0 mL)中之混合物18 h。將反應混合物倒入H2 O中並過濾。用H2 O清洗固體並在真空下乾燥以產生AG-2 。 向AG-2 (6.0 g，36.6 mmol)在AcOH (2.63 g，43.8 mmol)中之懸浮液中滴加KMnO4 (5.78 g，36.6 mmol)在H2 O (20.0 mL)中之溶液。在rt下攪拌該反應混合物15 h。用水稀釋該混合物並用EtOAc萃取。乾燥(Na2 SO4 )有機層，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生AG-3 。 在H2 (50 psi)下，在rt時攪拌AG-3 (3.3 g，16.8 mmol)及Pd/C (500 mg，10%在碳觸媒上)在MeOH (30 mL)中之溶液8 h。用N2 吹掃容器，過濾並濃縮濾液以產生AG-4 。 向AG-4 (2.5 g，12.5 mmol)在EtOAc (30 mL)中之攪拌溶液中添加在EtOAc中之HCl溶液(2N，20.0 mL)。在rt下攪拌該溶液5 h及然後將其過濾以產生中間物 AG 。MS (ES+)：m/z 201.2 [M+H]+ 。方法 9 ： 中間物 AH 之合成 在N2 下，在rt時攪拌AH-1 (113 g，0.62 mol)、K2 CO3 (171 g，1.24 mol)及乙硫醇鈉(67 g，0.80 mol)在DMF (2 L)中之混合物18 h。用H2 O稀釋該混合物並用EtOAc萃取。乾燥(Na2 SO4 )有機層，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生AH-2 。 在H2 (50 psi)下，在rt時攪拌AH-2 (20.0 g，0.12 mol)、RaNi (40 g)、Boc2 O (31.7g，0.14 mol)及TEA (24.5 g，0.24 mol)在THF (600 mL)中之溶液12 h。過濾該混合物並於減壓下濃縮濾液。藉由SiO2 急驟層析法純化所得殘餘物以產生AH-3。 在-10℃時向AH- 3 (65 g，0.24 mol)在AcOH (200 mL)中之懸浮液中滴加KMnO4 (45.8 g，0.29 mL)在水(500 mL)中之溶液。完成添加後，在rt下攪拌該反應混合物30 min。用H2 O稀釋該混合物並藉由添加水性Na2 CO3 鹼化至~pH 8並用EtOAc萃取。乾燥(Na2 SO4 )合併之有機層，傾析並濃縮。藉由結晶作用純化所得殘餘物以產生AH-4 。 在rt時向化合物AH-4 (46.5 g，0.15 mol)在MeOH (300 mL)中之攪拌溶液中添加在MeOH (300 mL)中之4M HCl並攪拌15 h。於減壓下濃縮該混合物。藉由結晶作用純化所得殘餘物以產生中間物 AH 。MS (ES+)：m/z 202.1 [M+H]+ 。方法 10 ： 中間物 AI 之合成 在100℃時攪拌AC (2 g，9.4 mmol)、AI-1 (4.8 g，18.8 mmol)、KOAc (2.8 g，28.2 mmol)及Pd(dppf)Cl2 (1.15 g，0.15 mmol)在1,4-二噁烷(40 mL)中之懸浮液18 h。冷卻至rt後，用水(10 mL)稀釋該混合物並用EtOAc (2x50 mL)萃取。乾燥(Na2 SO4 )合併之有機相，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生AI 。MS (ES+)：m/z 262.2 [M+H]+ 。方法 11 ： 中間物 AJ 之合成 向QQ (509 mg，1.1 mmol)在MeOH (4 mL)中之溶液中添加在二噁烷中之HCl溶液(4N，1.1 mL，4.4 mmol)。在rt下攪拌該反應混合物18 h。於減壓下濃縮該混合物。用乙醚研磨所得殘餘物並過濾以產生中間物 AJ-1 。 向AJ-1 (200 mg，0.55 mmol)在DCM (3 mL)中之溶液中添加TEA (0.77 mL，5.51 mmol)，接著添加AJ-2 (175 mg，1.10 mmol)。在rt下攪拌該反應混合物1 h，然後用水(5 mL)稀釋並用EtOAc (20 mL)萃取。乾燥(Na2 SO4 )有機層，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生中間物 AJ 。MS (ES+)：m/z 485.0 [M+H]+ 。方法 12 ： 中間物 AK 之合成 向AK-1 (2.00 g，13.1 mmol)在THF (25 mL)中之溶液中添加Boc2 O (3.45 mL，15.0 mmol)及TEA (3.64 mL，26.1 mmol)。在rt下攪拌該反應混合物18 h及然後用H2 O稀釋並用EtOAc萃取。濃縮有機層以產生AK-2 。 向AK-2 (3.3 g，13.1 mmol)在AcOH (10 mL)中之溶液中緩慢添加H2 O2 (1.37 mL，13.7 mmol)。在rt下攪拌該反應混合物3 h及然後用飽和Na2 SO3(aq) 中止並用1N NaOH(aq) 中和。用EtOAc萃取該混合物並濃縮以產生AK-3 。 向AK- 3 (1.0 g，3.7 mmol)、MgO (600 mg，14.9 mmol)、三氟乙醯胺(839 mg，7.4 mmol)及乙酸Rh(II)二聚物(115 mg，0.26 mmol)在DCM (10 mL)中之混合物中添加(二乙醯氧碘基)苯(1.79 g，5.6 mmol)。在rt下攪拌該混合物18 h及然後於減壓下濃縮。將所得殘餘物溶解於MeOH中，濾過矽藻土墊並向其添加K2 CO3 (2.55 g，18.6 mmol)。在rt下攪拌該混合物18 h並將其於減壓下濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生AK-4 。 向化合物AK-4 (585 mg，2.1 mmol)在DCM (2 mL)中之攪拌溶液中添加在二噁烷中之HCl溶液(4N，2 mL)。在rt下攪拌該反應混合物15 h及然後於減壓下濃縮以產生中間物 AK 。MS (ES+)：m/z 185.0 [M+H]+ 。方法 13 ： 中間物 AL 之合成 向AL-1 (500 mg，2.18 mmol)在ACN (12 mL)中之溶液中添加DIEA (0.46 mL，2.61 mmol)、Boc2 O (1.02 g，4.68 mmol)，接著添加DMAP (13.3 mg，0.11 mmol)。在rt下攪拌該反應混合物2.5 h。濃縮反應混合物並用EtOAc稀釋殘餘物並依序用H2 O及鹽水清洗，經Na2 SO4 乾燥，過濾並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AL-2 。 將AL-2 (250 mg，0.85 mmol)、Pd2 (dba)3 (39 mg，0.043 mmol)、Xanphos (41 mg，0.071 mmol)、Josiphos (13 mg，0.024 mmol)及TEA (0.83 mL，0.97 mmol)在甲苯(17 mL)中之混合物脫氣並加熱至115℃並保持1 h。然後使反應混合物冷卻至rt並添加乙硫醇(0.076 mL，1.02 mmol)。將反應混合物加熱至115℃並保持3 h。濃縮該反應混合物並藉由SiO2 急驟層析法純化殘餘物以產生AL-3 。 向AL-3 (200 mg，0.71 mmol)在丙酮(14 mL)中之溶液中添加過硫酸氫鉀(961 mg，1.56 mmol)在水(7 mL)中之溶液。在rt下攪拌反應混合物18 h。濃縮該混合物，然後用H2 O稀釋並用DCM萃取兩次。合併有機物並用鹽水清洗，經Na2 SO4 乾燥，過濾並濃縮以產生AL-4 。 向AL-4 (206 mg，0.67 mmol)在DCM (4 mL)中之溶液中添加在二噁烷中之HCl溶液(4N，1.68 mL，6.73 mmol)。在rt下攪拌該反應混合物2 h。濃縮反應混合物以產生呈HCl鹽之AL 。MS (ES+)：m/z 207.1 [M+H]+ 。方法 14 ： 中間物 AM 之合成 在0℃時向AM-1 (1 g，7.80 mmol)在THF (40 mL)中之溶液中添加DIEA (4.08 mL，23.40 mmol)，接著滴加氯甲酸苄酯(1.52 mL，10.14 mmol)。將反應混合物升溫至rt並攪拌過夜。然後濃縮反應混合物，用水稀釋及然後用EtOAc萃取。然後用飽和aq NaHCO3 (2X)、H2 O (2X)及鹽水清洗有機層，經MgSO4 乾燥，過濾並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AM-2 。 在0℃時向AM-2 (1 g，3.81 mmol)在THF (20 mL)中之溶液中滴加Br2 (0.30 mL，5.91 mmol)。將反應混合物升溫至rt並攪拌過夜。用水稀釋該反應混合物，然後用EtOAc萃取。然後用飽和aq NaHCO3 (2X)、水(2X)及鹽水清洗有機層，經MgSO4 乾燥，過濾並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AM-3 。 以類似中間物 AL-3 之方式合成AM-4 。 以類似中間物 AL-4 之方式合成AM- 5 。 向AM-5 (146 mg，0.41 mmol)在EtOH (10 mL)中之溶液中添加10% Pd/C (150 mg)及然後在H2 氣氛下，在rt時攪拌該混合物18 h。使反應混合物濾過矽藻土並用EtOAc清洗。濃縮濾液，然後添加在乙酸(1.5 mL，33重量%)中之HBr。在rt下攪拌該混合物2.5 h，然後過濾以產生呈HCl鹽之AM 。MS (ES+)：m/z 221.1 [M+H]+ 。方法 15 ： 中間物 AN 之合成 向AN-1 (6 g，3.99 mmol)在EtOH (60 mL)中之溶液中添加N2 H4 水合物(31.1 ml)。將該混合物加熱至回流並保持45 min。使該混合物冷卻至rt及然後將其濃縮。將殘餘物溶解於二乙二醇(20 mL)中並添加KOH (6.72 g，120 mmol)。在120℃下攪拌該混合物18 h。使該混合物冷卻至rt，用EtOAc稀釋並用1N HCl將pH調整至pH＜4。用鹽水清洗有機層，經Na2 SO4 乾燥並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AN-2 。 在0℃時向AN-2 (1.3 g，9.54 mmol)在DCM (20 mL)中之溶液中滴加Br2 (1.53 g，9.57 mmol)。在rt下攪拌該混合物12 h。用aq NaHSO3 中止該混合物並用DCM萃取兩次。合併有機層並用鹽水清洗，經Na2 SO4 乾燥並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AN-3 。 以類似中間物 AH-4 之方式合成AN-4 。 向AN-4 (800 mg，3.24 mmol)在NMP (10 mL)中之溶液中添加CuI (920 mg，4.83 mmol)及CuCN (397 mg，4.43 mmol)。在200℃時將微波反應加熱3 h。將該混合物倒入H2 O中，用EtOAc萃取。用鹽水清洗有機層，經Na2 SO4 乾燥並濃縮。藉由再結晶作用純化殘餘物以產生AN-5 。 以類似中間物 AH-3 之方式合成AN-6 。 以類似中間物 AH 之方式合成AN 。MS (ES+)：m/z 198.0 [M+H]+ 。方法 16 ： 中間物 AO 之合成 向保持在20℃以下之1-丙硫醇鈉(12.8 g，130 mmol)在ACN (150 mL)中之溶液中分批添加AG-1 (19.8 g，108 mmol)。然後在rt下攪拌該混合物16 h，將其倒入水(300 mL)中並用EtOAc (300 mL)萃取。乾燥(Na2 SO4 )合併之有機相，過濾並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AO-1 。 向保持在10℃以下之AO -1 (16.5 g，83.0 mmol)在AcOH (150 mL)中之攪拌溶液中滴加KMnO4 (14.5 g，92.0 mmol)在H2 O (150 mL)中之溶液。攪拌該反應混合物30 min。用水稀釋該混合物，藉由添加飽和aq Na2 CO3 鹼化並用EtOAc萃取。濃縮該溶液並藉由SFC純化殘餘物以產生AO-2 。 在H2 下，在rt時攪拌AO-2 (7.80 g，37.0 mmol)及Ra Ni (8.00 g)在MeOH (100 mL)中之混合物18 h。過濾及濃縮後，藉由MPLC純化殘餘物以產生AO-3 。 向固體AO-3 (7.40 g，35.0 mmol)中添加乙酸乙酯(2 mL)及在EtOAc (100 mL)中之HCl。在rt時攪拌該溶液5h並過濾固體以產生中間物 AO 。方法 17 ： 中間物 AP 之合成 在110℃時攪拌AP-1 (12.8 g，130 mmol)、環丙磺酸鈉(53.1 g，369 mmol)及CuI (23.3 g，123 mmol)在DMSO (150 mL)中之混合物2 h。冷卻至rt後，將該溶液倒入水中並用EtOAc萃取。經Na2 SO4 乾燥合併之有機相，過濾並濃縮。藉由MPLC純化所得殘餘物以產生AP-2 。 在H2 氣氛下，在rt時攪拌AP-2 (10.3 g，49 mmol)、Ra Ni (25.0 g)、Boc2 O (16.2 g，74 mmol)及TEA (10.0 g，99 mmol)在MeOH (250 mL)中之混合物18 h。過濾及濃縮後，藉由MPLC純化殘餘物以產生AP-3 。 向AP-3 (6.90 g，22 mmol)在MeOH (60 mL)中之溶液中添加在EtOH (60 mL)中之HCl。在rt時攪拌該溶液3 h並將其濃縮及再結晶以產生中間物 AP 。方法 18 ： 中間物 AQ 之合成 向AG-1 (82.0 g，448 mmol)在ACN (1.0 L)中之溶液中添加第三丁醇鈉(64.5 g)。使該混合物冷卻至0℃並滴加甲硫醇鈉(172.5 g，20%之 H2 O溶液)。然後容許在rt時攪拌該反應混合物16 h。添加水(800 mL)並用DCM萃取該混合物。用鹽水清洗合併之有機相，乾燥(Na2 SO4 )並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AQ-1 。 在5℃時向AQ-1 (51.5 g，343 mmol)在AcOH (500 mL)中之懸浮液中滴加KMnO4 (59.7 g，36.6 mmol)在H2 O (500.0 mL)中之溶液。然後在rt下攪拌該反應混合物1 h。用EtOAc萃取混合物，用aq. NaHCO3 清洗，乾燥(Na2 SO4 )並濃縮。藉由再結晶作用純化所得殘餘物以產生AQ-2 。 向AQ-2 (15.0 g，82 mmol)在MeOH (200 mL)中之溶液中添加Ra Ni (10.0 g)、TEA (34.4 mL)及Boc2 O (17.8 g)。在H2 (50 psi)下，攪拌該混合物12 h。用N2 吹掃容器，過濾並濃縮濾液。藉由SiO2 急驟層析法純化殘餘物以產生AQ-3 。 在rt時攪拌含於HCl之MeOH (500 mL)溶液中之AQ-3 (30.0 g，105 mmol)溶液12 h。濃縮該混合物並再結晶以產生中間物 AQ 。MS (ES+)：m/z 187 [M+H]+ 。 以類似中間物 AQ 之方式合成中間物 AR 及中間物 AS (MS (ES+)：m/z 202.1 [M+H]+ )。 方法 19 ： 中間物 AT 之合成 在rt時向AT-1 (10.0 g，55 mmol)、N,N-二甲基乙烷-1,2-二胺 (0.96 g，11 mmol)及三氟甲磺酸銅(II) (1.98，5 mmol)在DMSO (100 mL)中之混合物中添加AT -2 (8.27 g，98 mmol)。然後將該混合物加熱至120℃並保持30 min，用H2 O中止並用EtOAc萃取。乾燥有機層，濃縮並藉由SiO2 急驟層析法純化以產生AT-3 。 在H2 (15 psi)下，在rt時攪拌AT-3 (32.3 g，165 mmol)及Pd (3.50 g，33 mmol)在NH4 OH (30 mL)/EtOH (200 mL)中之混合物15 h。過濾該混合物，濃縮並藉由SiO2 急驟層析法純化以產生AT-4 。 向AT-4 (17.5 g，87 mmol)在EtOH(100 mL)中之攪拌溶液中添加在EtOH (100 mL)中之HCl。在rt下攪拌該溶液3 h及然後將其濃縮並再結晶以產生中間物 AT 。MS (ES+)：m/z 201 [M+H]+ 。方法 20 ： 中間物 AU 之合成 向AU-1 (7.15 g，26.5 mmol)在THF (50 mL)中之溶液中添加Boc2 O (6.70 mL，29.2 mmol)及TEA (7.40 mL，53.1 mmol)。容許在rt下攪拌該反應72 h。濃縮該溶液以產生AU-2 。 將AU-2 (5.25 g，15.8 mmol)、第三丁醇鈉(1.82 g，18.9 mmol)、Pd(OAc)2 (177 mg，0.79 mmol)及1,1’-雙(二異丙基膦基)二茂鐵(396 mg，0.95 mmol)之混合物添加至經氬氣吹掃之密閉容器中。添加二噁烷(35 mL)並在rt下攪拌該混合物1 h。添加三異丙基矽烷硫醇(3.72 mL，17.3 mmol)並將該溶液加熱至100℃並保持1 h。然後將該反應倒入EtOAc及水中。濃縮有機層並藉由SiO2 急驟層析法純化殘餘物以產生AU-3 。 將AU-3 (2.50 g，6.32 mmol)在THF (25 mL)中之溶液冷卻至0℃並用氬氣脫氣。然後添加溴化四丁基銨(2.12 g，7.58 mmol)並在0℃時攪拌該溶液1 h。然後添加溴乙腈(660 uL，9.48 mmol)並在0℃時攪拌該溶液5 min。濃縮該溶液並分配在乙醚與水之間。濃縮該有機層以產生AU-4 ，其無需進一步處理即可繼續使用。 向AU-4 (1.80 g，6.47 mmol)在ACN/H2 O (10 mL)中之溶液中添加過碘酸鈉(4.18 g，19.5 mmol)，接著添加氯化釕(III) (7.87 mg，0.038 mmol)。在rt下攪拌該反應混合物30 min及然後將其濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AU-5 。 向AU-5 (470 mg，1.51 mmol)在DCM (3 mL)中之攪拌溶液中添加在二噁烷(2.00 mL，8.00 mmol)中之HCl溶液。在rt下攪拌該溶液1 h並濃縮以產生中間物 AU 。MS (ES+)：m/z 211.1 [M+H]+ 。方法 21 ： 中間物 AV 之合成 在0℃時向濃HCl (200 mL)中添加AV-1 (20.0 g，168 mmol)，接著滴加aq NaNO2 (25.5 g在25 mL H2 O中)，保持＜5℃之內部溫度。容許在0℃時攪拌該溶液15 min及然後在5℃時將其緩慢添加至SO2 (108 g)及CuCl (84 mg)在AcOH (200 mL，＞ 5當量)中之混合物中。在5℃下攪拌該溶液90 min。用DCM (2 x 500 mL)萃取該反應混合物，乾燥(Na2 SO4 )並在下一步驟中直接使用AV-2 之有機溶液。 在0℃時向AV-2 (20.0 g，99 mmol)在DCM (200 mL)中之溶液中添加氨在MeOH (100 mL)中之溶液並在rt下攪拌30 min。將該混合物濃縮至乾燥並藉由SiO2 急驟層析法純化所得殘餘物以產生AV-3 。 向AV-3 (15.0 g，82 mmol)在MeOH (200 mL)中之溶液中添加Ra Ni (10.0 g)、TEA (34.4 mL)及Boc2 O (17.8 g)。在H2 (50 psi)下，在rt時攪拌該混合物12 h。用N2 吹掃容器，過濾並濃縮濾液。藉由SiO2 急驟層析法純化殘餘物以產生AV-4 。 在rt下攪拌含於HCl之MeOH(500 mL)溶液中之AV-4 (30.0 g，105 mmol)溶液12 h。濃縮並再結晶該混合物以產生中間物 AV 。MS (ES+)：m/z 188.1 [M+H]+ 。 以類似中間物 AV 之方式合成中間物 AW 。 方法 22 ： 中間物 (S)-AX 及 (R)-AX 之合成 在-30℃時向AG-3 (2.40 g，12 mmol)在THF (30 mL)中之溶液中滴加MeMgBr (30 mL)。添加後，在rt下攪拌該混合物4 h。藉由添加飽和aq NH4 Cl (100 mL)中止反應混合物並用EtOAc (3 x 100 mL)萃取。用鹽水清洗該有機相，經Na2 SO4 乾燥並於減壓下濃縮。藉由SiO2 急驟層析法純化殘餘物以產生AX-1 。 在0℃時向AX -1 (200 mg，1.0 mmol)在MeOH (2 mL)中之溶液中添加NH4 OAc (723 mg)及NaBH3 CN (41 mg)。在rt下攪拌該混合物16 h。於減壓下移除溶劑，添加水(50 mL)並將該混合物調整至pH＞12及然後用DCM (50 mL)萃取。經Na2 SO4 乾燥該有機相並濃縮。藉由預TLC純化殘餘物以產生AX -2 。 藉由SFC分離AX-2 以產生(S)-AX (67.9%ee)及(R)-AX (95.5%ee)。方法 23 ： 中間物 AY 之合成 向AY-1 (1.25 g, 5.49 mmol)在無水MeOH (15 mL)中之溶液中添加NaOMe (2.37 g, 43.89 mmol)。在rt下攪拌該混合物1 h。過濾該溶液並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生中間物 AY 。MS (ES+)：m/z 218.9 [M+H]+ 。方法 24 ： 中間物 AZ 之合成 向氫化鈉(342 mg，(60%)，8.57 mmol)在DMF (10 mL)中之溶液中添加無水異丙醇(360 uL, 4.71 mmol)。在rt下攪拌該混合物1 h。然後添加AB-1 (1.00 g，4.28 mmol)並再攪拌該混合物1 h，接著倒於冰上。然後用EtOAc萃取該混合物並濃縮。藉由SiO2 急驟層析法純化殘餘物以產生中間物 AZ 。MS (ES+)：m/z 258.8 [M+H]+ 。方法 25 ： 中間物 BA 之合成 使BA-1 (1.00 g，7.78 mmol)及Ni(dppe)Cl2 (82 mg，0.16 mmol)在無水Et2 O (5 mL)中之溶液冷卻至-10℃。然後，滴加正丙基溴化鎂並在-10℃下攪拌該混合物2 h。用飽和NH4 Cl中止該混合物，用DCM萃取並濃縮。粗製BA-2 無需進一步處理即可繼續使用。 在0℃時向BA-2 (1.0 g，7.34 mmol)在EtOH (10 mL)中之溶液中添加Br2 (379 uL，7.34 mmol)。在rt下攪拌該反應混合物2 h。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生中間物 BA 。MS (ES+)：m/z 217.4 [M+H]+ 。方法 26 ： 中間物 BC 之合成 使BA-1 (1.00 g，7.78 mmol)及Ni(dppe)Cl2 (82 mg，0.16 mmol)在無水Et2 O (5 mL)中之溶液冷卻至-10℃。滴加異丙基溴化鎂(3.22 mL，9.33 mmol)溶液並在-10℃下攪拌該混合物1 h。用飽和NH4 Cl中止該混合物，用DCM萃取並濃縮。粗製BC-1 以其本身之形式繼續使用。 在0℃時向BC-1 (1.0 g，7.34 mmol)在EtOH (10 mL)中之溶液中添加Br2 (378 uL，7.34 mmol)。在rt下攪拌該反應混合物2 h。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生中間物 BC 。MS (ES+)：m/z 216.4 [M+H]+ 。方法 27 ： 中間物 BD 之合成 使BA-1 (1.00 g，7.78 mmol)及Ni(dppe)Cl2 (82 mg，0.16 mmol)在無水Et2 O (5 mL)中之溶液冷卻至-10℃。滴加環丙基溴化鎂(1.36 g，8.56 mmol)溶液並在-10℃下攪拌該混合物2 h。用飽和水性NH4 Cl中止該混合物，用DCM萃取並濃縮。粗製BD-1 無需進一步處理即可繼續使用。 在0℃時向BD-1 (1.0 g，6.74 mmol)在EtOH (10 mL)中之溶液中添加Br2 (347 uL，6.74 mmol)。在rt下攪拌該反應混合物18 h。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生中間物 BD 。MS (ES+)：m/z 229.2 [M+H]+ 。方法 28 ： 中間物 BE 之合成 向BE-1 (40.0 g，244 mmol)在THF (800 mL)中之溶液中加入PPh3 (98.0 g)及NCS (160.0 g)。在80℃下攪拌該反應混合物10 h。然後用水中止該混合物並用EtOAc萃取。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生BE-2 。 向BE-2 (3.00 g，14.79 mmol)在甲苯及DMF中之攪拌溶液中添加Pd(PPh3 )4 (600 mg)、Pd(dppf)Cl2 (600 mg)及Na2 CO3 (6.27 g，59.17 mmol)。在90℃下攪拌該混合物5 h。用水中止該混合物，用EtOAc萃取。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生BE-3 。 在-10℃時向BE-3 (860 mg，5.0 mmol)在EtOH (5 mL)中之溶液中添加Br2 (347 uL，6.74 mmol)。在rt下攪拌該反應混合物18 h。濃縮該溶液並藉由SiO2 急驟層析法純化殘餘物以產生中間物 BE 。MS (ES+)：m/z 267 [M+H]+ 。方法 29 ： 中間物 BF 之合成 在-78℃時於30 min內向AB (6.00 g，26.2 mmol)及BF -1 (7.86 mL，34.1 mmol)在甲苯(60 mL)及THF (18 mL)中之溶液中滴加正丁基鋰(12.6 mL，31.4 mmol)。在-78℃下攪拌該溶液30 min及然後將其緩慢升溫至-20℃。用1 N HCl (40 mL)中止該溶液。然後分離該等層並用2M NaOH將水性層調整至pH~8。白色固體開始沉澱及使混合物在冷卻器中冷卻1 h。過濾固體以產生中間物 BF 。用MeTHF萃取水性層並濃縮以產生額外中間物 BF 。MS (ES+)：m/z 195.1 [M+H]+ 。中間物 BG 之合成 將正丁基鋰之己烷溶液(2.5 M，12.2 mL，30.5 mmol)於40 min內滴加至在甲苯(50 ml)及THF (12 ml)之混合物中之AC (5.00 g，23.5 mmol)及BF-1 (7.04 mL，30.5 mmol)的-78℃溶液中。在-78℃下攪拌該反應混合物30 min，在1 h 內將其升溫至-20℃並用HCl (50 mL，1N)中止。在周圍溫度下攪拌該所得混合物30 min，分離相並用NaOH (4M)將該水性層中和至pH~7。使渾濁之混合物冷卻至0℃並過濾所得沉澱以提供中間物 BG 。MS (ES+)：m/z 178.9 [M+H]+ 。方法 30 ： 中間物 BH 之合成 向2-甲基丙醛(5 g，69.34 mmol)及NH4 Cl (7.42 g，138.69 mmol)在水(50 mL)中之混合物中添加NaCN (4.08 g，83.2 mmol)。在rt下攪拌該混合物18 h。用EtOAc (3x)萃取該混合物。合併該等有機物，經Na2 SO4 乾燥，濃縮以產生無需進一步處理即可繼續使用的粗製中間物 BH 。方法 31 ： 中間物 BI 之合成 向BI-1 (20 mL，104 mmol)及2,2-二甲基環氧乙烷(15 mL，17 mmol)之混合物中一次性添加LiBr (1.86 g，21.4 mmol)。在rt下攪拌該反應混合物16 h。添加額外之2,2-二甲基環氧乙烷(2.0 mL，23 mmol)並在60℃下加熱該混合物2 h。用水中止反應混合物，然後用EtOAc萃取兩次。合併有機物並用鹽水清洗，經Na2 SO4 乾燥，過濾並濃縮以產生BI-2 。 在-21℃時向BI-2 (2.0 g，7.4 mmol)在DCM (20 mL)中之溶液中添加Deoxo-Fluor (1.51 mL，8.17 mmol)。添加後，在-21℃下攪拌該反應混合物5 min，然後用飽和aq NaHCO3 中止直至pH~8。分離層並用DCM萃取水性層。用飽和aq NaHCO3 清洗合併之有機物，經Na2 SO4 乾燥，過濾並濃縮以產生BI-3 。 向BI-3 (1.5 g，5.5 mmol)在甲苯(30 mL)中之溶液中滴加在二噁烷中之HCl溶液(4N，1.45 mL，5.80 mmol)。在rt下攪拌該反應混合物2 h，隨後過濾以產生BI-4 。 在Endeavor (60℃，400 psi)上將BI-4 (500 mg，1.62 mmol)、5% Pd/C (103 mg)及MeOH (3 mL)之混合物氫化5 h。使反應混合物濾過矽藻土並用MeOH清洗。濃縮濾液以產生呈HCl鹽之中間物 BI 。MS (ES+)：m/z 92.3 [M+H]+ 。方法 32 ： 中間物 BJ 之合成 向BJ-1 (7.40 mL，99.0 mmol)在DCM (100 mL)中之溶液中添加(R)-2-甲基-2-丙烷亞磺醯胺(10.0 g，82.5 mmol)、MgSO4 (49.66 g，412 mmol)及對甲苯磺酸吡啶鎓(1.04 g，4.13 mmol)。容許在rt下攪拌該反應混合物72 h。然後過濾反應混合物並藉由SiO2 急驟層析法純化殘餘物以產生BJ-2 。 向BJ-2 (9.72 g，56.1 mmol)在THF (200 mL)中之溶液中添加氟化四甲基銨(6.27 g，67.3 mmol)。用氬氣將該溶液脫氣及然後使其冷卻至-55℃。用額外之漏斗滴加三氟甲基三甲基矽烷(12.4 mL，84.1 mmol)在THF (250 mL)中之溶液及容許在-55℃下攪拌該反應2 h。然後容許將該反應混合物緩慢升溫至-10℃並用飽和水性NH4 Cl中止。用EtOAc萃取水性層並濃縮合併之有機層以產生無需進一步處理即可繼續使用之BJ-3 。 向BJ-3 (9.00 g，37.0 mmol)在MeOH (30 mL)中之溶液中添加在二噁烷(18.5 mL，74.0 mmol)中之4M HCl。容許在rt下攪拌該溶液1 h。然後將該反應混合物濃縮至一半體積並用乙醚稀釋直至形成白色沉澱。然後過濾該固體以產生中間物 BJ 。方法 33 ： 中間物 BK 之合 成向BK-1 (9.47 g，113 mmol)在DCM (100 mL)中之溶液中添加(R)-2-甲基-2-丙烷亞磺醯胺(10.5 g，86.6 mmol)、MgSO4 (52.1 g，433 mmol)及對甲苯磺酸吡啶鎓(1.09 g，4.33 mmol)。容許在rt下攪拌該反應混合物18 h。然後過濾該反應混合物並藉由SiO2 急驟層析法純化殘餘物以產生BK-2 。 在-50℃時向BK-2 (8.60 g，45.9 mmol)在DCM (350 mL)中之溶液中添加溴化甲基鎂(36.0 mL，108 mmol)。在-50℃下攪拌該溶液3 h。然後容許將該反應升溫至rt並攪拌18 h。用飽和水性NH4 Cl中止該溶液並用EtOAc (2X)萃取。濃縮有機層以產生無需進一步處理即可繼續使用之BK-3 。 向BK-3 (5.00 g，24.6 mmol)在MeOH (20 mL)中之溶液中添加在二噁烷(12.3 mL，49.2 mmol)中之4M HCl。容許在rt下攪拌該溶液1 h。然後濃縮該反應混合物並藉由SiO2 急驟層析法純化殘餘物以產生中間物 BK 。 以類似中間物 BK 之方式合成中間物 BL 以類似中間物 AJ 之方式合成中間物 BM (MS (ES+)：m/z 465.9 [M]+ )、BN (MS (ES+)：m/z 467.0 [M]+ )、BO (MS (ES+)：m/z 441.2 [M]+ )、BP (MS (ES+)：m/z 452.9 [M]+ )、BQ (MS (ES+)：m/z 441.0 [M]+ )、BR (MS (ES+)：m/z 441.0 [M]+ )、BS (MS (ES+)：m/z 467.0 [M]+ )。 方法 34 ： 中間物 BT 之合成 向2,4-二氯-嘧啶-5-基胺(3.03 g，18.1 mmol)在n-BuOH (40 mL)中之攪拌懸浮液中添加(1S,2S)-2-胺基-環戊醇鹽酸鹽(2.50 g，17.2 mmol)及DIEA (9.20 mL，51.8 mmol)。在130℃下攪拌該混合物4 h。然後於減壓下濃縮該反應混合物並在EtOAc及庚烷中將粗製產物研磨為固體並過濾以產生BT-1 。 向BT-1 (3.61 g，15.5 mol)在丙酮(200 mL)中之攪拌溶液中添加K2 CO3 (5.34 g，38.6 mmol)及氯-側氧基-乙酸乙酯(1.94 mL，17.0 mmol)。在rt下攪拌該混合物1 h。過濾該反應混合物並於減壓下濃縮濾液。將粗製酮酯溶解於無水EtOH (50 mL)中，放置於耐壓燒瓶中，並添加TEA (5.43 mL，38.6 mmol)。將此加熱至130℃並保持1 h。於減壓下濃縮該反應混合物並將其溶解於EtOAc (100 mL)中。依序用水(2 x 20 mL)及鹽水(20 mL)清洗有機層並乾燥(Na2 SO4 )，傾析並濃縮。在EtOAc及庚烷中將該所得殘餘物研磨為固體以產生BT-2 。 向BT-2 (500 mg，1.73 mmol)在DCM (100 mL)中之混合物中添加戴斯-馬丁(Dess-Martin)過碘烷(2.25 g，5.20 mmol)並在rt下攪拌該混合物96 h。用飽和NaHCO3 (50 mL)清洗該混合物並乾燥(Na2 SO4 )有機層並於減壓下濃縮。將該固體殘餘物兩次懸浮於DCM (50 mL)中，超音波處理並過濾。將所得固體再懸浮於EtOAc (20 mL)中並超音波處理。過濾該固體產物以產生BT-3 。 在rt時向BT-3 (124 mg，0.442 mmol)在DCM (6 mL)中之混合物中添加草醯氯(0.076 mL，0.88 mmol)，接著滴加無水DMF (0.30 mL，3.9 mmol)直至固體溶解。在rt下攪拌該混合物30 min，而LCMS指示未反應之初始材料。向該混合物中添加更多草醯氯(0.048 mL，0.55 mmol)並再攪拌該混合物10 min。在氮氣流下，在35℃時使該反應濃縮1 h並直接使用所得殘餘物BT-4 。 在rt時向BT-4 (132 mg，0.442 mmol)及AG (105 mg，0.442 mmol)在DMF (2 mL)中之攪拌溶液中添加TEA (0.311 mL，2.21 mmol)並在rt下攪拌該混合物15 min。向該反應混合物中添加水(50 mL)並以EtOAc (3 x 50 mL)萃取此混合物。合併有機層，乾燥(Na2 SO4 )，傾析並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生中間物 BT 。MS (ES+)：m/z 463.1 [M+H]+ 。方法 35 ： 實例 9 之合成。 將中間物AB (27 mg，0.12 mmol)、雙(頻哪醇)二硼(30 mg，0.12 mmol)、乙酸鉀(35 mg，0.36 mmol)及[1,1'-雙二苯基膦基二茂鐵]-二氯化鈀(II)(9 mg，0.011 mmol)合併於經脫氣之甲苯/DME/乙醇/水(3:2:2:1，3 mL)之溶液中。在微波反應器中將容器加熱至90℃並保持20 min。在一獨立容器中，將中間物A (50 mg，0.12 mmol)、雙(頻哪醇)二硼(30 mg，0.12 mmol)、KOAc (35 mg，0.36 mmol)及雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (8 mg，0.011 mmol)合併於經脫氣之1,4-二噁烷(3 mL)中。在微波反應器中將該反應加熱至90℃並保持20 min。合併兩容器之內容物並添加Na2 CO3(aq) (2M，1 mL)。在微波反應器中將該反應加熱至120℃並保持30 min。使該容器冷卻至rt並過濾內容物並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生實例 9 。MS (ES+)：m/z 537.2 [M+H]+ 。實例 11 之合成。 將中間物AC (252 mg，1.18 mmol)、雙(頻哪醇)二硼(600 mg，2.36 mmol)、乙酸鉀(348 mg，2.36 mmol)及[1,1'-雙二苯基膦基二茂鐵]-二氯化鈀(II)(95 mg，0.118 mmol)合併於經脫氣之甲苯/DME/乙醇/水(3:2:2:1，3 mL)之溶液中。在微波反應器中將容器加熱至90℃並保持20 min。在一獨立容器中，將中間物A (500 mg，1.18 mmol)、雙(頻哪醇)二硼(600 mg，2.36 mmol)、乙酸鉀(348 mg，2.36 mmol)及雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (84 mg，0.118 mmol)合併於經脫氣之1,4-二噁烷(3 mL)中。在微波反應器中將該反應加熱至90℃並保持20 min。合併兩容器之內容物並添加Na2 CO3(aq) (2M，1 mL)。在微波反應器中將該反應加熱至120℃並保持30 min。使該容器冷卻至rt並過濾內容物並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生實例 11 。MS (ES+)：m/z 521.4 [M+H]+ 。實例 15 之合成。 將中間物AE (283 mg，1.18 mmol)、雙(頻哪醇)二硼(600 mg，2.36 mmol)、乙酸鉀(348mg，3.54 mmol)及[1,1'-雙二苯基膦基二茂鐵]-二氯化鈀(II)(95 mg，0.12 mmol)合併於經脫氣之甲苯/DME/乙醇/水(3:2:2:1，3 mL)之溶液中。在微波反應器中將容器加熱至90℃並保持20 min。在一獨立容器中，將中間物A (500 mg，1.18 mmol)、雙(頻哪醇)二硼(600 mg，2.36 mmol)、乙酸鉀(348 mg，3.54 mmol)及雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (84 mg，0.12 mmol)合併於經脫氣之1,4-二噁烷(3 mL)中。在微波反應器中將該反應加熱至90℃並保持20 min。合併兩容器之內容物並添加2M碳酸氫鈉(1 mL)。在微波反應器中將該反應加熱至120℃並保持30 min。使該容器冷卻至rt並過濾內容物並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生實例 15 。MS (ES+)：m/z 547.4 [M+H]+ 。實例 17 之合成。 將中間物AB (52 mg，0.23 mmol)、雙(頻哪醇)二硼(58 mg，0.23 mmol)、KOAc (67 mg，0.23 mmol)及[1,1'-雙二苯基膦基二茂鐵]-二氯化鈀(II)(18 mg，0.23 mmol)合併於經脫氣之甲苯/DME/乙醇/水(3:2:2:1，3 mL)之溶液中。在微波反應器中將容器加熱至90℃並保持20 min。在一獨立容器中，中間物G (100 mg，0.23 mmol)、雙(頻哪醇)二硼(58 mg，0.23 mmol)、KOAc (67 mg，0.69 mmol)及雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (16 mg，0.023 mmol)合併於經脫氣之1,4-二噁烷(3 mL)中。在微波反應器中將該反應加熱至90℃並保持20 min。合併兩容器之內容物並添加Na2 CO3(aq) (2M，1 mL)。在微波反應器中將該反應加熱至120℃並保持30 min。使該容器冷卻至rt並過濾內容物並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生實例 17 。MS (ES+)：m/z 551.4 [M+H]+ 。實例 63 之合成。 將中間物AB (105 mg，0.46 mmol)、雙(頻哪醇)二硼(175 mg，0.69 mmol)、乙酸鉀(67mg，0.69 mmol)及[1,1'-雙二苯基膦基二茂鐵]-二氯化鈀(II)(18 mg，0.045 mmol)合併於經脫氣之甲苯/DME/乙醇/水(3:2:2:1，3 mL)之溶液中。在微波反應器中將容器加熱至90℃並保持20 min。在一獨立容器中，將中間物B (100 mg，0.23 mmol)、雙(頻哪醇)二硼(175 mg，0.69 mmol)、KOAc (67 mg，0.69 mmol)及雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (16 mg，0.045 mmol)合併於經脫氣之1,4-二噁烷(3 mL)中。在微波反應器中將該反應加熱至90℃並保持20 min。合併兩容器之內容物並添加2M碳酸氫鈉(1 mL)。在微波反應器中將該反應加熱至120℃並保持30 min。使該容器冷卻至rt並過濾內容物並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生實例 63 。MS (ES+)：m/z 548.0 [M+H]+ 。實例 65 之合成。 將中間物AC (174 mg，0.820 mmol)、雙(頻哪醇)二硼(277 mg，1.093 mmol)、乙酸鉀(161mg，1.64 mmol)及[1,1'-雙二苯基膦基二茂鐵]-二氯化鈀(II)(43 mg，0.055 mmol)合併於經脫氣之甲苯/DME/乙醇/水(3:2:2:1，3 mL)之溶液中。在微波反應器中將容器加熱至90℃並保持20 min。在一獨立容器中，將中間物X (247 mg，0.547 mmol)、雙(頻哪醇)二硼(277 mg，0.820 mmol)、乙酸鉀(161 mg，1.64 mmol)及雙(二第三丁基(4-二甲基胺基苯基)膦)二氯鈀(II) (43 mg，0.055 mmol)合併於經脫氣之1,4-二噁烷(3 mL)中。在微波反應器中將該反應加熱至90℃並保持20 min。合併兩容器之內容物並添加Na2 CO3(aq) (2M，1 mL)。在微波反應器中將該反應加熱至120℃並保持30 min。使該容器冷卻至rt並過濾內容物並濃縮。藉由SiO2 急驟層析法純化所得殘餘物以產生實例 65 。MS (ES+)：m/z 550.0 [M+H]+ 。 以類似方式製造下列化合物： 實例1-8 、 10 、 12-14 、 16 、 18-62 、 64 、 66-92 、 129 。方法 36 ： 實例 93 之合成。 用氬氣吹掃AJ (100 mg，0.21 mmol)、中間物AI (83.7 mg，0.32 mmol)、K3 PO4 (91 mg，0.43 mmol)及Pd(dppf)Cl2 (26 mg，0.03 mmol)在1,4-二噁烷(2 mL)中之混合物，及然後添加H2 O (0.25 mL)。在100℃下攪拌該混合物18 h。冷卻至rt後，用水(2 mL)稀釋該混合物並用EtOAc (2x5 mL)萃取。乾燥(Na2 SO4 )合併之有機相，傾析並濃縮。藉由逆向HPLC純化所得殘餘物以產生實例 93 。MS (ES+)：m/z 584.0 [M+H]+ 。實例 136 之合成。 用氬氣吹掃NNN (3500 mg，8.05 mmol)、中間物BG (2149 mg，12.07 mmol)、K3 PO4 (3417 mg，16.09 mmol)及Pd(dppf)Cl2 (986 mg，1.21 mmol)在1,4-二噁烷(60 mL)中之混合物，及然後添加H2 O (6 mL)。在100℃下攪拌該混合物18 h。冷卻至rt後，用水(2 mL)稀釋該混合物並用EtOAc (2x5 mL)萃取。乾燥(Na2 SO4 )合併之有機相，傾析並濃縮。藉由逆向HPLC純化所得殘餘物以產生實例 136 。MS (ES+)：m/z 533.0 [M+H]+ 。實例 158 之合成 用氬氣吹掃MMM (3360 mg，7.49 mmol)、中間物BG (2664 mg，14.97 mmol)、K3 PO4 (3177 mg，14.97 mmol)及Pd(dppf)Cl2 (916 mg，1.12 mmol)在1,4-二噁烷(60 mL)中之混合物，及然後添加H2 O (6 mL)。在100℃下攪拌該混合物18 h。冷卻至rt後，用水(2 mL)稀釋該混合物並用EtOAc (2x5 mL)萃取。乾燥(Na2 SO4 )合併之有機相，傾析並濃縮。藉由逆向HPLC純化所得殘餘物以產生實例 158 。MS (ES+)：m/z 539.3 [M+H]+ 。 以類似方式製造下列化合物： 實例94-128 、 130-132 、 134 、 137-144 、 146-157 、 159-199 、 201-265 。 方法 37 ： 實例 133 之合成： 用氬氣吹掃AC (5.39 g，25.3 mmol)、雙(頻哪醇)二硼(10.4 g，40.5 mmol)、乙酸鉀(3.98 g，40.5 mmol)及Pd(dppf)Cl2 DCM錯合物(0.83 g，1.01 mmol)在DME/Tol/EtOH/H2 O (10:6:3:1)中之混合物，密封並在80℃時攪拌30 min。將此混合物添加至經氬氣吹掃之BU-1 (根據在方法1之步驟1及步驟2中描述之程序合成) (2.70 g，10.1 mmol)及Pd(amphos)Cl2 (0.71 g，1.01 mmol)之混合物中並將經密封之混合物加熱至110℃並保持2 h。然後濃縮該混合物，用EtOAc稀釋，過濾並再次濃縮。藉由SiO2 急驟層析法純化粗製物以產生BU-2 。 向BU-2 (856 mg，2.35 mmol)在DCM (15 ml)中之溶液中添加草醯氯(596 mg，4.70 mmol)，接著添加5滴DMF。容許攪拌該反應18 h。然後濃縮該反應及殘餘物產出BU-3 ，其以本身形式繼續使用。 在rt時向BU-3 (150 mg，0.36 mmol)在DMF中之攪拌溶液中添加DIEA (196 uL，1.41 mmol)。10分鐘後添加BU-4 (84.1 mg，0.42 mmol)並在rt下攪拌該反應10 min。然後濃縮該混合物並藉由逆向HPLC (NH4 CO3 )純化以產生實例 133 。MS (ES+)：m/z 509.1 [M+H]+ 。 以類似實例 133 之方式合成實例 135 及 145 。 方法 38 ： 實例 200 之合成： 向216 (100 mg，0.195 mmol)在二噁烷(2 mL)/水(1 mL)中之溶液中添加LiOH (28.0 mg，1.17 mmol)。在rt下攪拌該反應16 h。濃縮該混合物並將其溶解於水中，用1N HCl將其酸化至pH~5，過濾，用水清洗並在真空烘箱中乾燥以產生200 。MS (ES+)：m/z 498.1 [M+H]+ 。生物活性 本發明之化合物具有作為RORγ (與視網酸受體相關之孤兒受體γ)調節劑之活性。 報導子基因分析(RGA) 進行核受體轉活化分析以定量測試化合物抑制螢光素酶報導子之RORγ轉活化的能力。在Khan等人，Bioorganic & Medicinal Chemistry Letters 23 (2013)，532-536中描述類似分析。該系統使用經兩個質體(pGL4.3，luc2P/GAL4UAS/Hygro及pBIND，Gal4DBD hRORC LBD1-3)共轉染之經瞬時轉染之HEK 293細胞。陽性對照係經兩個質體共瞬時轉染，及陰性對照含有pGL4.3啟動子序列。將分析組合於384孔盤中，在此孔盤中，經瞬時轉染之細胞及測試化合物以不同之濃度培養20-24 h。次日，取出分析盤並在RT下平衡20-30分鐘。使用Bright-Glo™螢光素酶分析系統檢測螢光素酶生產量。添加Bright GLO檢測試劑後，在RT下培養該等盤20分鐘。在Envision盤讀取器上讀取該等盤以測量發光訊號。將RLU訊號轉換為與對照孔及空白孔相關的POC。 細胞接種培養基： RPMI 1640-Invitrogen #11875135)、2.5% FBS-Invitrogen # 26140、1xPenicillin-Streptomycin-Gibco # 15140 化合物稀釋緩衝液： 1X HBSS-Invitrogen #14025126 分析盤：Greiner #781080-020 Bright Glo螢光素酶分析系統：Promega #E2620 融化提供在套組中之溶解緩衝液，向受質粉末添加100 mL溶解緩衝液。 下表呈現在上述分析中測試本發明之化合物時所獲得之結果，該等結果證明其等作為RORγ調節劑的活性： 表II：報導子基因分析中之生物活性表 治療用途之方法 基於本發明之式(I)之化合物或其互變異構物、外消旋物、鏡像異構物、非鏡像異構物、其混合物及所有上文提及之形式之鹽的生物性質，其皆適用於治療自體免疫及過敏性疾病，因為其對RORγ展示良好調節效應。 因此本發明係關於通式(I)之化合物及其醫藥上可接受之鹽及所有互變異構物、外消旋物、鏡像異構物、非鏡像異構物、其混合物，該等物質可用於治療其中RORγ調節劑之活性具有治療效益之疾病及/或病症，包含(但不限於)治療自體免疫或過敏性疾病。 可藉由本發明之化合物治療之此類疾病包含例如：類風濕性關節炎、牛皮癬、全身性紅斑狼瘡、狼瘡性腎炎、全身性硬化症、脈管炎、硬皮病、氣喘病、過敏性鼻炎、過敏性濕疹、多發性硬化症、幼年類風濕性關節炎、幼年特發性關節炎、I型糖尿病、克羅恩氏病、潰瘍性結腸炎、移植物抗宿主病、牛皮癬性關節炎、反應性關節炎、關節黏連性脊椎炎、動脈粥樣硬化、葡萄膜炎及非放射線脊椎關節病。 為治療上述疾病及病症，治療有效劑量通常將在約0.01 mg至約10 mg/kg體重/本發明之化合物劑量的範圍內；較佳地，自約0.1 mg至約5 mg/kg體重/劑量。例如，向70 kg之人投與時，劑量範圍為約0.7 mg至約750 mg/劑量本發明之化合物，較佳自約7.0 mg至約350 mg/劑量。可能需要一定程度的常規劑量最優化以判定最佳給藥水平及模式。每日可投與1至6次活性成分。一般投與及醫藥組合物 當作為藥物使用時，通常以醫藥組合物之形式投與本發明之化合物。此類組合物可使用醫藥領域所熟知的程序來製備且其通常包括至少一種本發明之化合物及至少一種醫藥上可接受之載劑。本發明之化合物亦可單獨投與或與具有以下作用之佐劑組合使用：增強本發明之化合物之穩定性，促進在某些實施例中含有該等佐劑之醫藥組合物之投與，提供經增強之溶解性或分散性、經增強之拮抗劑活性，提供輔助性治療及類似情況。本發明之化合物可單獨使用或結合本發明之其他活性物質使用，視需要亦可結合其他藥理學活性物質。一般言之，本發明之化合物可以治療有效量或醫藥有效量投與，但出於診斷或其他目的亦可較少量投與。 可使用可接受之醫藥組合物之投與模式中之任何一種實施呈純形式或呈適當之醫藥組合物之形式投與本發明的化合物。因此，該投與可係例如經口、經頰(例如，經舌下)、經鼻、非經腸、經局部、透皮、經陰道或經直腸，呈固體、半固體、凍乾粉或液體劑型之形式，諸如，例如，錠劑、栓劑、丸劑、軟彈性明膠膠囊及硬明膠膠囊、粉劑、溶液、懸浮液或霧劑或類似物，較佳呈適合簡單投與精確劑量之單位劑型。該等醫藥組合物通常將包含習知的醫藥載劑或賦形劑及作為該/一活性劑之本發明之化合物及此外，可包含其他藥劑、醫藥品試劑、載劑、佐劑、稀釋劑、媒劑或其組合。熟習此項技術者已知此類醫藥上可接受之賦形劑、載劑或添加劑及製造用於各種模式或投與之醫藥組合物的方法。以下文獻可證實此項技術之當前發展水平例如：Remington：The Science and Practice of Pharmacy，第20版，A. Gennaro (編)，Lippincott Williams & Wilkins，2000；Handbook of Pharmaceutical Additives，Michael & Irene Ash (編)，Gower，1995；Handbook of Pharmaceutical Excipients，A. H. Kibbe (編)，American Pharmaceutical Ass'n，2000；H. C. Ansel及N. G. Popovish，Pharmaceutical Dosage Forms and Drug Delivery Systems，第5版，Lea及Febiger，1990；該等文獻中之各者以全文引用的方式併入本文中以更適當地描述此項技術之當前發展水平。如熟習此項技術者將預期，用於特定藥物調配物中之本發明之化合物的形式將經選擇(例如，鹽)，以具有使該調配物有效所需之合適的物理特徵(例如，水溶性)。 以全文引用的方式將本申請案中引述之所有專利或非專利文獻或文獻資料併入本文中。 Definitions and protocols used The terms that are not explicitly defined herein have the meanings of those skilled in the art in light of the disclosure and the scope of the disclosure. As used herein, unless otherwise stated, the following definitions apply: Prefix CXy The use (where x and y each represent a natural number) indicates that the combination of the chain or ring structure or the chain and ring structure as a whole in direct contact with the specification and the reference may be composed of carbon atoms of a maximum value y and a minimum value x. In general, for a group comprising two or more subgroups, unless otherwise stated, the last named subgroup attachment point, for example, the substituent "aryl-C"1-3 -alkyl" means bonding to C1-3 An aryl group of an alkyl group bonded to a core or group to which the substituent is attached. However, if the bond is described just before the first named subgroup, the first named subgroup is attached to the group, for example, the substituent "-S(O)n C1-6 Alkyl" means bonding to S(O)n Group C1-6 An alkyl group to which the former is bonded to a core or group to which the substituent is attached. Alkyl represents a monovalent, saturated hydrocarbon chain which may exist in the form of a straight chain (no branch) and a branched chain. If the alkyl group is substituted, the substitutions can occur independently of one another (in each case mono- or poly-substituted) on all hydrogen-carrying carbon atoms. For example, the term "C1-5 "Alkyl" contains, for example, H3 C-, H3 C-CH2 -, H3 C-CH2 -CH2 -, H3 C-CH (CH3 )-, H3 C-CH2 -CH2 -CH2 -, H3 C-CH2 -CH(CH3 )-, H3 C-CH (CH3 )-CH2 -, H3 C-C (CH3 )2 -, H3 C-CH2 -CH2 -CH2 -CH2 -, H3 C-CH2 -CH2 -CH(CH3 )-, H3 C-CH2 -CH(CH3 )-CH2 -, H3 C-CH (CH3 )-CH2 -CH2 -, H3 C-CH2 -C(CH3 )2 -, H3 C-C (CH3 )2 -CH2 -, H3 C-CH (CH3 )-CH(CH3 )-and H3 C-CH2 -CH(CH2 CH3 )-. Other examples of alkyl groups are methyl (Me; -CH)3 ), ethyl (Et; -CH)2 CH3 ), 1-propyl (n-propyl; n-Pr; -CH)2 CH2 CH3 ), 2-propyl (i-Pr; isopropyl; -CH(CH)3 )2 ), 1-butyl (n-butyl; n-Bu; -CH)2 CH2 CH2 CH3 ), 2-methyl-1-propyl (isobutyl; i-Bu; -CH2 CH(CH3 )2 ), 2-butyl (second butyl; sec-Bu; -CH (CH)3 )CH2 CH3 ), 2-methyl-2-propyl (t-butyl; t-Bu; -C(CH)3 )3 ), 1-pentyl (n-pentyl; -CH)2 CH2 CH2 CH2 CH3 ), 2-pentyl (-CH(CH)3 )CH2 CH2 CH3 ), 3-pentyl (-CH(CH)2 CH3 )2 ), 3-methyl-1-butyl (isopentyl; -CH)2 CH2 CH(CH3 )2 ), 2-methyl-2-butyl (-C(CH)3 )2 CH2 CH3 ), 3-methyl-2-butyl (-CH(CH)3 )CH(CH3 )2 ), 2,2-dimethyl-1-propyl (neopentyl; -CH)2 C(CH3 )3 ), 2-methyl-1-butyl (-CH)2 CH(CH3 )CH2 CH3 ), 1-hexyl (n-hexyl; -CH)2 CH2 CH2 CH2 CH2 CH3 ), 2-hexyl (-CH(CH)3 )CH2 CH2 CH2 CH3 ), 3-hexyl (-CH(CH)2 CH3 ) (CH2 CH2 CH3 )), 2-methyl-2-pentyl (-C(CH)3 )2 CH2 CH2 CH3 ), 3-methyl-2-pentyl (‐CH(CH)3 )CH(CH3 )CH2 CH3 ), 4-methyl-2-pentyl (-CH(CH)3 )CH2 CH(CH3 )2 , 3-methyl-3-pentyl (-C(CH)3 ) (CH2 CH3 )2 ), 2-methyl-3-pentyl (-CH(CH)2 CH3 )CH(CH3 )2 ), 2,3-dimethyl-2-butyl (-C(CH)3 )2 CH(CH3 )2 ), 3,3-dimethyl-2-butyl (-CH(CH)3 )C(CH)3 )3 ), 2,3-dimethyl-1-butyl (-CH)2 CH(CH3 )CH(CH3 )CH3 ), 2,2-dimethyl-1-butyl (-CH)2 C(CH3 )2 CH2 CH3 ), 3,3-dimethyl-1-butyl (-CH)2 CH2 C(CH3 )3 ), 2-methyl-1-pentyl (-CH)2 CH(CH3 )CH2 CH2 CH3 ), 3-methyl-1-pentyl (-CH)2 CH2 CH(CH3 )CH2 CH3 ), 1-heptyl (n-heptyl), 2-methyl-1-hexyl, 3-methyl-1-hexyl, 2,2-dimethyl-1-pentyl, 2,3-dimethyl -1-pentyl, 2,4-dimethyl-1-pentyl, 3,3-dimethyl-1-pentyl, 2,2,3-trimethyl-1-butyl, 3-ethyl Alkyl-1-pentyl, 1-octyl (n-octyl), 1-indenyl (n-decyl), 1-indenyl (n-decyl), and the like. The terms propyl, butyl, pentyl, hexyl, heptyl, octyl, decyl, decyl and the like without any other definition mean a saturated hydrocarbon group having the corresponding number of carbon atoms, which contains all isomeric forms. If the alkyl group is another (combined) group (such as, for example, CXy Alkylamino group or CXy In the case of a part of alkoxy), the definition of the above alkyl group is also employed. Unlike an alkyl group, an alkenyl group (when used alone or in combination) consists of at least two carbon atoms, wherein at least two adjacent carbon atoms are linked together by a CC double bond and the carbon atom can only be a CC double bond. Part of it. If in an alkyl group having at least two carbon atoms as defined above, two hydrogen atoms on adjacent carbon atoms are formally removed and the free valence is saturated to form a second bond, thereby forming the corresponding alkenyl group. The alkenyl group may optionally be present in a cis or trans or E or Z orientation for the double bond. Unlike alkyl, alkynyl (when used alone or in combination) consists of at least two carbon atoms, wherein at least two adjacent carbon atoms are linked together by a C-C triple bond. If in the alkyl group having at least two carbon atoms as defined above, each of the two hydrogen atoms on the adjacent carbon atom is formally removed and the free valence is saturated to form the other two bonds, thereby forming the corresponding alkynyl group. . Haloalkyl (haloalkenyl, haloalkynyl) (when used alone or in combination) is derived from a previously defined alkyl (alkenyl, alkynyl) in a manner such that one or more of the hydrocarbon chains The hydrogen atoms are replaced independently of each other by halogen atoms (which may be the same or different). If a haloalkyl group (haloalkenyl, haloalkynyl) is to be further substituted, the substitutions can occur independently of one another (in each case in the form of a mono- or poly-substitution) on all hydrogen-carrying carbon atoms. An example of a haloalkyl (haloalkenyl, haloalkynyl) group is -CF3 , -CHF2 , -CH2 F, -CF2 CF3 -CHFCF3 , -CH2 CF3 , -CF2 CH3 ,-CHFCH3 , -CF2 CF2 CF3 , -CF2 CH2 CH3 , -CF=CF2 , -CCl=CH2 , -CBr=CH2 ,-C≡C-CF3 ,-CHFCH2 CH3 ,-CHFCH2 CF3 Wait. Halogen is a fluorine, chlorine, bromine and/or iodine atom. The term "cycloalkyl" (when used alone or in combination) means a non-aromatic 3 to 12 member (but preferably 3 to 6 member member) monocyclic carbocyclic group or a non-aromatic 6 to 10 member fused bicyclic ring. , bridged bicyclic, propane or spiro carbocyclic groups. C3-12 The cycloalkyl group can be saturated or partially saturated, and the carbocyclic ring can be attached by any atom of the ring to produce a stable structure. Non-limiting examples of 3- to 10-membered monocyclic carbocycles include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, cycloheptenyl, and cyclohexyl ketone. Non-limiting examples of 6 to 10 membered fused bicyclic carbocyclyl groups include bicyclo[1.1.1]pentane, bicyclo[3.3.0]octane, bicyclo[4.3.0]nonane, and bicyclo[4.4.0]癸Base (decalinyl). Non-limiting examples of 6 to 10 membered bicyclic carbocyclic groups include bicyclo [2.2.2] heptyl, bicyclo [2.2.2] octyl and bicyclo [3.2.1] octyl. Non-limiting examples of 6 to 10 membered propane alkane ring groups include, but are not limited to, [1.1.1.] propane, [3.3.3] propane, and [3.3.1] propane. Non-limiting examples of 6 to 10 membered spirocyclic carbocyclic groups include, but are not limited to, spiro[3,3]heptyl, spiro[3,4]octyl, and spiro[4,4]heptyl. The term "heterocyclyl" (when used alone or in combination) means having from 2 to 10 carbon atoms and from 1 to 4 selected from the group consisting of NH, NR', oxygen and sulfur (wherein R' is C1-6 Heteroatom ring atoms of alkyl) and containing a stable non-aromatic 4 to 8 membered monocyclic heterocyclic ring or a stabilized non-aromatic 6 to 11 membered fused bicyclic, bridged bicyclic or spirocyclic heterocyclic ring system . The heterocyclic ring can be fully saturated or partially saturated. In one embodiment, the heterocyclic system C3-6 A heterocyclic ring, that is, it contains 3 to 6 ring carbon atoms. Non-limiting examples of non-aromatic monocyclic heterocyclic groups include tetrahydrofuranyl, azetidinyl, pyrrolidinyl, piperidyl, tetrahydropentanyl, dioxoalkyl, thiomorpholinyl, 1 , 1-di- oxy-1.λ6 - thiomorpholinyl, morpholinyl, piperidinyl, piperazinyl and azepinyl. Non-limiting examples of non-aromatic 6 to 11 member fused bicyclic groups include octahydrofluorenyl, octahydrobenzofuranyl and octahydrobenzothiophenyl. Non-limiting examples of non-aromatic 6 to 11 member bridged bicyclic groups include 2-azabicyclo[2.2.1]heptyl, 3-azabicyclo[3.1.0]hexane and 3-azabicyclo[ 3.2.1] Octyl group. Non-limiting examples of non-aromatic 6 to 11-membered spirocyclic heterocyclic groups include 7-aza-spiro[3,3]heptyl, 7-spiro[3,4]octyl and 7-aza- Spiro[3,4]octyl. Sulfur and nitrogen may be present in all possible oxidation stages (sulfur à 碸-SO-, 碸-SO)2 -; nitrogen à N-oxide). The term "aryl" (when used alone or in combination) refers to an aromatic hydrocarbon ring containing from six to fourteen carbon ring atoms (eg, C)6-14 Aryl group, preferably C6-10 Aryl). Term C6-14 The aryl group includes a monocyclic ring, a fused ring, and a bicyclic ring, wherein at least one of the rings is an aromatic ring. C6-14 Non-limiting examples of aryl groups include phenyl, indanyl, indenyl, benzocyclobutane, dihydronaphthyl, tetrahydronaphthyl, naphthyl, benzocycloheptyl, and benzocycloheptane Alkenyl. As used herein, the term "heteroaryl" (when used alone or in combination) means having from 2 to 10 carbon atoms and from 1 to 4 selected from N, NH, NR', O and S (wherein R' C1-6 a hetero atom ring atom of an alkyl group and comprising an aromatic 5 to 6 membered monocyclic heteroaryl group and an aromatic 7 to 11 membered heteroaryl bicyclic or fused ring (wherein at least one of the rings is an aromatic ring) a heteroaryl ring system). Non-limiting examples of 5- to 6-membered monocyclic heteroaryl rings include furyl, oxazolyl, isoxazolyl, oxadiazolyl, piperidyl, thiazolyl, pyrazolyl, pyrrolyl, imidazolyl, Tetrazolyl, triazolyl, thienyl, thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl and anthracenyl. Non-limiting examples of 7 to 11 membered heteroaryl bicyclic or fused rings include benzimidazolyl, 1,3-dihydrobenzimidazol-2-one, quinolyl, dihydro-2H-quinolyl, Isoquinolyl, quinazolinyl, oxazolyl, thieno[2,3-d]pyrimidinyl, fluorenyl, isodecyl, oxazolyl, benzotriazolyl, benzofuranyl, Benzopyridyl, benzodioxolyl, benzoxazolyl, benzothiazolyl, pyrrolo[2,3-b]pyridyl and imidazo[4,5-b]pyridine base. Sulfur and nitrogen may be present in all possible oxidation stages (sulfur à 碸-SO-, 碸-SO)2 -; nitrogen à N-oxide). The compounds of the present invention are only those of ordinary skill in the art that are considered to be chemically stable. For example, a compound having a "floating price" or a carbon anion is a compound not encompassed by the methods of the invention disclosed herein. Unless otherwise stated, the chemical formula or name will include tautomers and all stereo, optical, and geometric isomers (eg, mirror image isomers, non-image isomers) throughout the specification and the accompanying claims. , E/Z isomers, etc.) and racemates thereof, mixtures of individual mirror image isomers in different ratios, mixtures of non-image isomers or mixtures of any of the foregoing, in which Isomers and mirror image isomers and salts (including pharmaceutically acceptable salts thereof) and their corresponding unsolvated forms and solvated forms with pharmaceutically acceptable solvents such as water, ethanol and the like. The compounds of the invention also include isotopically labeled forms thereof. The isotopically labeled form of the active agent of the present invention is the same as the active agent, but in practice one or more of the atoms of the active agent have been atomized with an atomic mass or mass different from the atom normally found in nature. The mass or mass number is replaced by more than one atom. Examples of isotopes that are readily available and can be incorporated into the active agents of the combinations of the present invention according to well established procedures include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, fluorine, and chlorine, for example,2 H,3 H,13 C,14 C,15 N,18 O,17 O,31 P,32 P,35 S,18 F and36 Cl. Also acceptable within the scope of the invention are the active agents of the present invention, prodrugs thereof, or pharmaceutically acceptable salts containing one or more of the above isotopes and/or other isotopes of other atoms. The phrase "pharmaceutically acceptable" as used herein means that they are suitable for contact with human and animal tissues without reasonable toxicity, irritating, allergic reactions or other problems or complications within the scope of sound medical judgment. A reasonable benefit/risk ratio of a compound, material, composition, and/or dosage form. Pharmaceutically acceptable salts include those derived from pharmaceutically acceptable inorganic and organic acids and bases. Examples of suitable acids include hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, perchloric acid, fumaric acid, maleic acid, phosphoric acid, glycolic acid, lactic acid, salicylic acid, succinic acid, toluene-p-sulfuric acid, tartaric acid, acetic acid. , citric acid, methanesulfonic acid, formic acid, benzoic acid, malonic acid, naphthalene-2-sulfuric acid and benzenesulfonic acid. Other acids, such as oxalic acid, although they are themselves non-pharmaceutically acceptable, can be used in the preparation of salts useful as intermediates in obtaining such compounds and their pharmaceutically acceptable acid addition salts. Other pharmaceutically acceptable salts can be formed from cations of metals such as aluminum, calcium, lithium, magnesium, potassium, sodium, zinc, and the like (see also Pharmaceutical salts, Birge, SM et al, J. Pharm. Sci., (1977),66 , 1-19). The pharmaceutically acceptable salts of the present invention can be synthesized from nucleophilic compounds containing basic or acidic moieties by conventional chemical methods. In general, such salts may be prepared by combining the free acid or base forms of such compounds with sufficient base or acid in water or an organic diluent such as diethyl ether, ethyl acetate, ethanol, isopropanol or acetonitrile or mixtures thereof. The reaction is prepared. For the purposes of the present invention, a therapeutically effective amount means an amount of a substance which ameliorates the symptoms of the disease or alleviates such symptoms, or prolongs the survival time of the treated patient.Embodiment of the present invention A general embodiment of the invention relates to a compound of the following formula (I) or a pharmaceutically acceptable salt thereof:(I) where: R1 Department: –CN; –S(O)n R6 ;–S(O)n NR7 R8 ;–S(O)(NR9 )R6 ; –N(R9 )C(O)R6 ;–N(R9 )C(O)OR6 ;–N(R9 )S(O)n R6 ; –C(O)OR9 ; –C(O)NR7 R8 ; or –C(O)R9 ; or R1 R6 , R7 , R8 Or R9 Can be cyclized on W to form a ring; and R2 And R3 Independently: (A) – H; (B) C, as required, substituted by one, two or three groups selected from the following:1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; c) –CN; d) –CF3 ; e) – halo; f) –C(O)OR9 ; g) –C(O)N(R9 )2 ; h) –S(O)n R9 ; and i) –S(O)n NR7 R8 ; or (C) C3-6 Cycloalkyl; (D) C3-6 Heterocyclic group; or R2 And R3 Forming C together with the carbon to which it is attached3-6 Carbocycle; or R2 And R3 Forming C together with the carbon to which it is attached3-6 Heterocycle; or R2 Or R3 Can be cyclized on W to form a ring; R4 Line: (A) C, if necessary, substituted by one, two or three groups selected from the following1-6 Alkyl: a) C3-6 Cycloalkyl; b) C3-6 Heterocyclic group; c) –OR9 ; d) –CN; e) –S(O)n R9 ; f) – halo; and g) – CF3 Or (B) C, as required, substituted by one, two or three groups selected from the following:3-12 Cycloalkyl: a) C1-6 Alkyl; b) –OR9 ; c) –CN; d) –S(O)n R9 ; e) – halo; and f) – CF3 Or (C) an aryl, heteroaryl or heterocyclic group optionally substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –S(O)n R9 ; f) – halo; and g) – CF3 ; R5 An aryl group, a heteroaryl group, a heterocyclic group or a C which may be substituted with one, two or three groups selected from the following:3-12 Cycloalkyl: (A) C, if desired, substituted by one, two or three groups selected from the group consisting of1-6 Alkyl, C3-6 Cycloalkyl or C3-6 Heterocyclic group: a) C3-6 Cycloalkyl; b) C3-6 Heterocyclic group; c) –OR9 ; d) –CN; e) –S(O)n NR7 R8 ; f) –S(O)n R9 ; g) – halo; and h) –CF3 ; or (B) –OR9 ; (C) –CN; (D) –CF3 ; (E) – halo; (F) – S(O)n NR7 R8 ; (G) –S(O)n R9 ; and (H) –NR7 R8 ; W is an aryl group, a heteroaryl group, a heterocyclic group, or a C which may be substituted with one or two groups selected from the following:3-12 Cycloalkyl or alkynyl: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 ; f) – halo; g) – NR7 R8 ; h) –C(O)OR9 ; and i) –C(O)N(R9 )2 ;R6 Is selected from: (A) -OH; (B) C, if desired, substituted by one or two groups selected from the following1-6 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; c) –CN; d) –CF3 ; and e) – halo; (C) C3-6 Cycloalkyl; and (D) –CF3 ; R7 And R8 Is independently selected from: (A) -H; (B) C, if desired, substituted by one or two groups selected from the following:1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; c) –CN; d) –halogen; and (C) C3-6 Cycloalkyl; or R7 And R8 Together with the nitrogen bonded thereto, a saturated ring having 3 to 6 carbon atoms is formed, wherein one of the carbon atoms of the saturated ring can be optionally subjected to -O-, -NR9 – or –S(O)n – replacement; R9 Is selected from: (A) – H; (B) C substituted by one or two groups selected from the following:1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; c) –CN; d) –CF3 ; and e) – halo; or (C) C3-6 a cycloalkyl group; and n is a 0, 1 or 2. Additional sub-embodiments within the various substituent definitions include the following:R 1 Group embodiment (1) R1 Department: –CN; –S(O)n R6 ;–S(O)n NR7 R8 ; –N(H)S(O)n R6 ; or –S(O)(NH)R6 ; and where: R6 Line: (A) C substituted by one or two groups selected from the following:1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; and c) –CN; or (B) C3-6 Cycloalkyl; R7 And R8 Independently: (A) – H; or (B) C1-3 Alkyl; and R9 Line from: (A) –H; (B) C1-3 Alkyl; or (C) C3-6 a cycloalkyl group; and a n system of 1 or 2. (2) R1 Department: -S(O)n R6 ; -S(O)n NR7 R8 ; or -S(O)(NH)R6 ; and where: R6 Line: (A) C substituted by one or two groups selected from the following:1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; and c) –CN; or (B) C3-6 Cycloalkyl; R7 And R8 Independently: (A) – H; or (B) C1-3 Alkyl; and R9 Line from: (A) –H; (B) C1-3 Alkyl; or (C) C3-6 a cycloalkyl group; and a n system of 1 or 2. (3) R1 Department –S(O)n R6 , –S(O)n NR7 R8 Or –S(O)(NH)R6 ; and R6 Department C1-3 Alkyl; and R7 And R8 Independently: (A) – H; or (B) C1-3 Alkyl; and n is 2.R 2 and R 3 Group embodiment (1) R2 And R3 Each of the lines is independently selected from: (A) - H; (B) C, if desired, substituted by one, two or three groups selected from the group consisting of1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 ; or c) – halo; and R2 And R3 Forming C together with the carbon to which it is attached3-6 Carbocycle; or R2 And R3 Forming C together with the carbon to which it is attached3-6 Heterocycle; and R9 Lines are selected from: (A) –H; and (B) C1-3 alkyl. (2) R2 And R3 Each line is independently selected from: (A) – H; and (B) C1-3 Alkyl; (3) R2 And R3 H.R 4 Group embodiment (1) R4 Line: (A) C, if necessary, substituted by one, two or three groups selected from the following1-6 Alkyl: a) C3-6 Cycloalkyl; b) 4, 5 or 6 membered heterocyclic; c) –OR9 ; d) –CN; e) –halogen; and f) –CF3 Or (B) C, as required, substituted by one, two or three groups selected from the following:3-6 Cycloalkyl: a) C1-6 Alkyl; b) –OR9 ; c) –CN; d) –halogen; and e) –CF3 ; and where the C3-6 One of the cycloalkyl groups may be replaced by -O-; (C) phenyl; or (D) 4, 5 or 6 membered heterocyclic; and R9 Lines are selected from: (A) –H; and (B) C1-3 alkyl. (2) R4 Line: (A) C substituted by one or two groups selected from the following:1-6 Alkyl: a) C3-6 Cycloalkyl; b) 4, 5 or 6 membered heterocyclic; c) –OR9 ; d) –CN; e) –halogen; and f) –CF3 Or (B) C, as required, substituted by one, two or three groups selected from the following:3-6 Cycloalkyl: a) C1-6 Alkyl; b) –OR9 ; c) –CN; d) –halogen; and e) –CF3 Or (C) phenyl; or (D) 4, 5 or 6 membered heterocyclic; and R9 Department C1-3 alkyl. (3) R4 Department: (A) one or two selected from C as needed3-6 Cycloalkyl, halo, –CF3 And C1-3 Alkoxy group substituted C1-6 Alkyl; or (B) one or two selected from C as needed1-6 Alkyl, –CF3 And a group substituted with a halogen group3-6 a cycloalkyl group; or (C) a 5-membered heterocyclic group.R 5 Group embodiment (1) R5 An aryl, heteroaryl or heterocyclic group optionally substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 ; f) – halo; and g) – NR7 R8 ; and R7 , R8 And R9 Each line is independently selected from: (A) – H; and (B) C1-3 alkyl. (2) R5 Line: (A) A phenyl group substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 And f) - a halogen group; or (B) a 5 or 6 membered heteroaryl group substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 ; f) – halo; and g) – NR7 R8 ; and R7 , R8 And R9 Each line is independently selected from: (A) – H; and (B) C1-3 alkyl. (3) R5 A pyridyl or pyrimidinyl group optionally substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CF3 ; and e) –NR7 R8 ; and R7 And R8 Each line is independently selected from: (A) – H; (B) C1-3 Alkyl; and R9 Department C1-3 alkyl. (4) R5 A pyrimidinyl group which is optionally substituted with one or two groups selected from the group consisting of: a) C1-3 Alkyl; b) C3-5 Cycloalkyl; c) C1-3 Alkoxy; and d) –CF3 .W Group embodiment (1) W is optionally substituted with one or two groups selected from the group consisting of phenyl, pyridyl, pyrimidinyl, piperidinyl, piperazinyl, pyrazinyl or C.3-12 Cycloalkyl: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 ; f) – halo; g) – NR7 R8 ; h) –C(O)OR9 ; and i) –C(O)N(R9 )2 ;R7 , R8 And R9 Each line is selected from: (A) – H; and (B) C1-3 alkyl. (2) W is a phenyl group, a pyridyl group, a pyrimidinyl group or a piperidinyl group. Additional embodiments include the above R1 , R2 , R3 , R4 , R5 , R6 And any possible combination of the sub-embodiments of W.formula (I) Additional subordinate embodiment Further sub-genus examples of the compound of the above formula (I) include: (1) a compound of the above formula (I) or a pharmaceutically acceptable salt thereof, wherein: R1 Department: –S(O)nR6 ; –S(O)nNR7 R8 ; or –S(O)(NH)R6 ; R2 And R3 Each line is independently selected from: (A) – H; and (B) C1-3 Alkyl; R4 Line: (A) C substituted by one or two groups selected from the following:1-6 Alkyl: a) C3-6 Cycloalkyl; b) 4, 5 or 6 membered heterocyclic; c) –OR9 ; d) –CN; e) –halogen; and f) –CF3 (B) C, if necessary, substituted by one, two or three groups selected from the following3-6 Cycloalkyl: a) C1-6 Alkyl; b) –OR9 ; c) –CN; d) –halogen; and e) –CF3 (C)phenyl; or (D) 5 or 6 membered heterocyclic; R5 Line: (A) A phenyl group substituted with one or two groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 And f) - a halogen group; or (B) a pyridyl or pyrimidinyl group optionally substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 ; f) – halo; and g) – NR7 R8 And W are each optionally substituted with one or two groups selected from the group consisting of phenyl, pyridyl, pyrimidinyl, piperidinyl or C.3-12 Cycloalkyl: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CN; e) –CF3 ; f) – halo; g) – NR7 R8 ; h) –C(O)OR9 ; and i) –C(O)N(R9 )2 ;R6 Line: (A) C substituted by one or two groups selected from the following:1-3 Alkyl: a) C3-6 Cycloalkyl; b) –OR9 And b) –CN; or (B) C3-6 Cycloalkyl; R7 , R8 And R9 Independently: (A) – H; or (B) C1-3 Alkyl; and n is 2. (2) A compound of the above formula (I) or a pharmaceutically acceptable salt thereof, wherein: R1 Department –S(O)n R6 Or –S(O)n NR7 R8 ; and R2 And R3 H; R4 Department: (A) one or two selected from C as needed3-6 Cycloalkyl, –CF3 And C1-3 Alkoxy group substituted C1-6 Alkyl; or (B) one or two selected from C as needed1-6 C substituted by alkyl, -CN and halo groups3-6 Cycloalkyl; or (C) 5-membered heterocyclic group; R5 A pyrimidinyl group which is substituted with one, two or three groups selected from the group consisting of: a) C1-6 Alkyl; b) C3-6 Cycloalkyl; c) –OR9 ; d) –CF3 ; and e) –NR7 R8 ;W is phenyl, pyridyl, pyrimidinyl or piperidinyl; R6 Department C1-3 Alkyl; R7 , R8 , R9 Independently: (A) – H; or (B) C1-3 Alkyl; and n is 2. (3) A compound of the formula (I), or a pharmaceutically acceptable salt thereof, as described immediately above in (2), wherein: R5 A pyrimidinyl group which is optionally substituted with one or two groups selected from the group consisting of: a) C1-3 Alkyl; b) C3-5 Cycloalkyl; and c) C1-3 Alkoxy; and W is a phenyl, pyridyl, pyrimidinyl or piperidinyl group. Particular compounds within the scope of the invention comprise a compound of the following Table I or a pharmaceutically acceptable salt thereof: Table I also provides physicochemical data for all prepared compounds (i.e., HPLC residence time and mass spectrometry data). The HPLC method is defined in the Synthesis Examples section below. The invention further relates to pharmaceutically acceptable salts of the compounds of formula (I) with inorganic or organic acids or bases. In another aspect, the invention relates to a compound of formula (I) - or a pharmaceutically acceptable salt thereof - as a medicament. In another aspect, the invention relates to a method of treating a patient, wherein the compound of formula (I), or a pharmaceutically acceptable salt thereof, is used. In another aspect, the invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of autoimmune diseases and allergic diseases. In another aspect, the invention relates to the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, for the manufacture of a pharmaceutical composition for the treatment of autoimmune diseases and allergic diseases. In another aspect, the invention relates to a method for treating an autoimmune disease and an allergic disease, comprising administering to a patient a therapeutically effective amount of a compound of formula (I) - or a pharmaceutically acceptable Salt. In another aspect, the invention relates to a pharmaceutical composition comprising as an active substance one or more compounds of formula (I) - or a pharmaceutically acceptable salt thereof - optionally combined with conventional excipients and/or Carrier. The compounds of formula (I) can be made using the general synthetic methods described below, and such methods also form part of the invention.General synthetic method The compounds of the present invention can be prepared by synthetic methods, synthetic examples, methods known to those of ordinary skill, and methods documented in the chemical literature. In the synthetic methods and examples described below, the substituent R1 , R2 , R3 , R4 , R5 And W should have the meanings as defined above in the detailed description of the compounds of formula I. The methods described herein are intended to be illustrative, and are not intended to limit the scope of the invention. Where the preparation of the initial compounds is not described, they are commercially available, can be prepared analogously to the compounds or methods described herein or described in the chemical literature. Unless otherwise stated, one of ordinary skill in the art can readily select solvents, temperatures, pressures, and other reaction conditions. Formula R1 -W-C(R2 )(R3 )-NH2 The amine intermediates are commercially available; or may be prepared according to the general procedures or references described in US 7,879,873 and WO 2011/049917; or may be prepared by the skilled artisan using methods described in the chemical literature. The compound of formula (I) can be prepared from intermediate A' according to Scheme I. Flowchart IAs shown in Scheme I, a suitable pyrimidine of formula A' (where G is NH)2 , X is a group suitable for palladium media cross-coupling reactions (eg, I, Br, Cl or OSO)2 CF3 ), and Y is a suitable leaving group (for example, Cl)) and formula R4 NH2 a suitable amine or amine salt (eg, a hydrochloride salt) such as isopropylamine in a suitable base (eg, i-Pr2 EtN or Et3 The reaction of the compound of formula B' is provided in the presence of N) in a suitable solvent (e.g., n-butanol) and under suitable reaction conditions such as a suitable temperature (e.g., about 120 ° C). Alternatively, the pyrimidine of formula A' (where G is NH)2 Suitable synthetic precursors (eg, nitro) can be combined with formula R4 NH2 Suitable amine or amine salts (eg, hydrochlorides) such as 1-methylcyclopropylamine in suitable reagents and solvents (eg, i-Pr, respectively)2 The reaction is carried out in the presence of EtN and THF) under suitable reaction conditions such as a suitable temperature (e.g., about -78 ° C to about 25 ° C) to provide an intermediate which may be in a suitable reagent (for example, NO)2 Groups such as SnCl can be used2 The appropriate reagent is reduced) and further converted to a compound of formula B'. Those skilled in the art will be able to use the formula R for the above reaction.4 NH2 The selection of a suitable amine and a pyrimidine of formula A&apos; can be based on criteria such as the amine and the spatial and electronic properties of the pyrimidine. The diaminopyrimidine of formula B' can be combined with a suitable reagent such as chloro-o-oxy-ethyl acetate in a suitable solvent (e.g., acetone) and in a suitable base (e.g., K)2 CO3 The reaction is carried out in the presence of a compound of formula C'. The carbonyl compound of formula C' can be combined with a suitable dehydrochlorinating reagent such as chloroform chloride in the presence of a suitable additive (for example, a catalytic amount of DMF) in a suitable solvent (for example, CH)2 Cl2 And reacting under suitable reaction conditions such as a suitable temperature (e.g., about ambient temperature) to provide a compound of formula D'. Chloro-pteridin of formula D' can be combined with formula R1 -W-C(R2 )(R3 )-NH2 a suitable amine or amine salt such as 4-ethanesulfonylbenzylamine in a suitable base (eg, Et3 The compound of formula E' is produced in the presence of N) in a suitable solvent (e.g., THF) and under suitable reaction conditions (such as a suitable temperature (e.g., about ambient temperature)). The pyrimidine of formula E' can be combined with a suitable cross-coupling partner (for example,Acid) and a suitable base (for example, K3 PO4 In a suitable solvent (eg, 1,4-dioxane), a suitable cross-coupling catalyst (eg, Pd(dppf)Cl2 Heating in the presence of a suitable reaction condition such as a suitable atmosphere (e.g., argon) and a suitable temperature (e.g., about 100 ° C) to provide a compound of formula (I).Synthesis example Non-limiting examples of methods of making the compounds of the invention are provided below. The optimum reaction conditions and reaction times will vary depending upon the particular reagent employed. Unless otherwise stated, one of ordinary skill in the art can readily select solvents, temperatures, pressures, and other reaction conditions. Specific procedures are provided in the Synthesis Examples section. The intermediates and products can be purified by chromatography, recrystallization and/or reverse phase HPLC (RHPLC) on silica gel. Discrete image isomers can be obtained by isolating the racemic product using palm HPLC. The RHPLC purification method uses 0-100% acetonitrile in water containing 0.1% formic acid or 0.1% TFA and uses one of the following columns: a) Waters Sunfire OBD C18 5 μM 30x150 mm column b) Waters XBridge OBD C18 5 μM 30x150 mm column c) Waters ODB C8 5 μM 19x150 mm column d) Waters Atlantis ODB C18 5 μM 19x50 mm column e) Waters Atlantis T3 OBD 5 μM 30x100 mm column f) Phenomenex Gemini Axia C18 5 μM 30x100 mm column HPLC method: Analytical LC/MS analysis method A: Column: Waters BEH 2.1x50mm C18 1.7um column gradient: Analytical LC/MS Analytical Method B: Column: Waters BEH 2.1x50mm C18 1.7um Column Gradient: A list of abbreviations used in the synthesis example: method 1 : Intermediate A Synthesis toA-1 (3.00 g, 18.18 mmol) added to a stirred suspension in n-butanol (10 mL)A-2 (10.80 g, 18.18 mmol) followed by DIEA (6.46 mL, 36.58 mmol). The mixture was stirred at 120 ° C for 17 h. Cool the reaction to rt and add saturated aqueous NH4 The Cl solution was stopped. The reaction was then diluted with EtOAc. The organic layer was separated and washed with water, then brine. Dry (Na2 SO4 The organic layer was decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceA-3 . toA-3 (1.00 g, 5.00 mmol) Add oxalic acid ethyl ester (0.88 g, 6.43 mmol) to a stirred suspension in acetone (100 mL), then add K2 CO3 (1.85 g, 13.39 mmol). The mixture was stirred at rt for 18 h and the solid precipitate was separated to giveA-4 . toA-4 (1.14 g, 5.00 mmol) in CH2 Cl2 Grassy chlorine (1 mL) was added to the stirred suspension in (250 mL) followed by 5 drops of DMF. The mixture was stirred at rt for 5 h. The mixture is then concentrated under reduced pressure to produceA-5 . toA-5 (0.1 g, 0.39 mmol) TEA (0.16 mL, 1.16 mmol) (or DIEA) was added to a stirred suspension in THF (4 mL).AG (91 mg, 0.38 mmol). The reaction was allowed to stir at rt for 18 h. By adding saturated aqueous NH4 The reaction was quenched with Cl and extracted with EtOAc. Wash the organic layer with water and brine and dry (Na2 SO4 ), decanted and concentrated under vacuum. By SiO2 Purification of the resulting residue by flash chromatography to produceIntermediate A . MS (ES+): m/z 423.0 [M+H]+ .method 2 : Intermediate B Synthesis At -78 ° C, toB-1 (1.80 g, 9.30 mmol) andB-2 (1.00 g, 9.30 mmol) DIEA (3.29 mL, 18.59 mmol) was added to a stirred suspension of THF (10 mL) and the reaction was slowly warmed to 25 °C. The volatiles were removed under reduced pressure and the crude was redissolved in EtOAc.2 O cleaning. Separate the organic layer and use H2 O Wash more than twice. Wash the organic layer with brine and dry (Na2 SO4 ), decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceB-3 . toB-3 (1.78 g, 7.79 mmol) Add SnCl to a solution in EtOH (50 mL)2 (1.48 g, 7.79 mmol) and heated to reflux for 4 h. The reaction was allowed to cool to rt and then poured onto ice. With 1N NaOH(aq) The solution was treated to bring the pH to ~9 and then filtered through a pad of diatomaceous earth. Separate the organic phase and first use H2 O Wash and rinse with salt water. Dry (Na2 SO4 The organic layer was decanted and concentrated. By SiO2 Purification of the crude product by flash chromatography to produceB-4 . As an alternative procedure for the reduction of nitropyrimidines to the corresponding aminopyrimidines, the following general procedure has been applied to similar intermediates: Catalyst RaNi is added to a solution of nitropyrimidine in EtOH. Pump down the reaction vessel and take N2 (g) Purify, then evacuate and take H2 (g) Filling. In H2 (g) The reaction was maintained for 15 h in an atmosphere. Take time out of the container and take N2 (g) Purge. The reaction was filtered through a pad of celite to remove the Ni catalyst and the filtrate was concentrated. By SiO2 The resulting residue was purified by flash chromatography to afford the corresponding aminopyrimidine. toB-4 (0.40 g, 2.01 mmol) added K in a stirred solution of acetone (10 mL)2 CO3 (0.70 g, 5.06 mmol) followed by chloroethyl ester (0.27 mL, 2.43 mmol). The reaction was stirred at rt for 24 h. Then filter the reaction and dissolve it in H2 O was extracted with EtOAc. The aqueous phase was separated and extracted twice more with EtOAc. Combine the organic phases and dry (Na2 SO4 ), decanted and concentrated to produceB-5 . toB-5 (0.70 g, 2.77 mmol) in CH2 Cl2 Grassy chlorine (0.47 mL, 5.54 mmol) was added to the solution in (50 mL) followed by 5 drops of DMF. The reaction was allowed to stir at rt for 18 h. The volatiles were removed in vacuo. Redissolve the crude in DCM and pour H2 O. The organic layer was separated, washed with brine and dried (Na2 SO4 ), decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceB-6 . toB-6 (0.83 g, 3.06 mmol) DIEA (1.07 mL, 6.12 mmol) was added to a stirred solution in THF (10 mL)AF (0.72 g, 3.06 mmol). The reaction was stirred at rt for 18 h. The volatiles were removed in vacuo and the crude residue was resuspended in DCM and poured into H2 O. The aqueous phase was separated and extracted twice more with DCM. The organic layers were combined, washed with brine and dried (Na2 SO4 ), decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceIntermediate B . MS (ES+): m/z 434.1 [M+H]+ . The following intermediates were prepared in a similar manner: (Note: The oxalic acid produced by the reaction of A-3 (Method 1) and B-4 (Method 2) with chloroethyl oxalate can be isolated as described in Method 34. The ethyl ester intermediate is heated with a suitable base (such as TEA) in a suitable solvent (such as EtOH) at a suitable temperature (e.g., 130 ° C) to provide the corresponding intermediates A-4 and B-5, respectively. method 3 : Intermediate AB Synthesis toAB-1 (300 mg, 1.29 mmol) NaOMe (208 mg, 3.86 mmol). The mixture was stirred at rt for 1 h. The solution was filtered and concentrated. By SiO2 Purification of the residue by flash chromatography to produceIntermediate AB . MS (ES+): m/z 230.8 [M+H]+ .method 4 : Intermediate AC Synthesis toAC-1 (320 mg, 2.07 mmol), 2,4,6-trimethyl-1,3,5,2,4,6-trioxaborane (520 mg, 4.14 mmol) and aq Na2 CO3 (2M, 3.1 mL, 6.21 mmol) in dioxane (10 mL) was added dichloropalladium 4-dibutylphosphino-N,N-dimethylaniline (73 mg, 0.10 mmol) . The mixture was heated to 130 ° C in a microwave reactor for 40 min. The mixture was diluted with MeOH (5 mL) filtered and concentrated. By SiO2 Purification of the residue by flash chromatography to produceAC-2 . At -10 ° CAC-2 (363 mg, 2.71 mmol) of Br in Br in EtOH (10 mL)2 (432 mg, 2.71 mmol). The reaction mixture was stirred at rt for 18 h. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceIntermediate AC . MS (ES+): m/z 214.3 [M+H]+ .method 5 : Intermediate AD Synthesis Stirring at 16 ° CAD-1 (100.0 g, 0.70 mol), a mixture of formazan acetate (146 g, 1.4 mol) and NaOMe (266.0 g, 4.9 mol) in MeOH (2 L) for 2 days. The reaction mixture was neutralized to pH 7 with acetic acid and filtered. Concentrate the filtrate under reduced pressure and pass SiO2 Purification of the crude product by flash chromatography to produceAD- 2 . At 0 °CAD-2 (66.0 g, 0.48 mol) and TEA (145.1 g, 1.44 mol) in TCM (1.5 L) in a stirred solution of Tf2 A solution of O (164.2 g, 0.58 mol) in DCM (500 mL) was stirred for 3 h. By adding H2 O (200 mL) was quenched and extracted with DCM (3×500 mL). Saturated aq NaHCO3 Wash the combined organic phase and dry (Na2 SO4 ), decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceAD-3 . At the time of reflow at N2 Stirring in the atmosphereAD-3 (17.0 g, 0.06 mol), vinylAcid pinacol ester (29.3 g, 0.09 mol), K2 CO3 (26.3 g, 0.19 mol), Ag2 O (1.7 g, 10% by weight) and Pd(dppf)Cl2 (1.7 g, 10% by weight) a mixture of anhydrous THF (400 mL) for 18 h. The mixture was allowed to cool to rt and filtered. Concentrate the filtrate under reduced pressure and pass SiO2 Purification of the resulting residue by flash chromatography to produceAD-4 . In H2 Stirring in the atmosphereAD-4 (27.3 g, 0.28 mol) and a mixture of RaNi (30.0 g, 10% by weight) in EtOH (500 mL) for 16 h. Use N2 Purge the container and filter the contents. The filtrate was concentrated under reduced pressure and used directly.AD-5 (19.6 g). At -10 ° CAD-5 (19.6 g, 0.13 mol) Add Br to a stirred solution in EtOH (300 mL)2 (52.9 g, 0.33 mol). After the addition, the mixture was stirred at rt for 30 min. By adding 10% Na2 S2 O3 (aq) Solution to stop the reaction mixture and add 10% Na2 CO3 (aq) The solution was basified to adjust to ~pH 8. The mixture was extracted with EtOAc (3 x 200 mL). Combine organic layers and dry (Na2 SO4 ), decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceIntermediate AD . MS (ES+): m/z 228.9 [M+H]+ .method 6 : Intermediate AE Synthesis toAC-1 (2.50 g, 16.17 mmol), cyclopropylAcid (4.17 g, 48.51 mmol) and Na2 CO3 (aq) (2M, 24.26 mL, 48.51 mmol) bis(di-t-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) in dioxane (30 mL) (572.5 mg, 0.81 mmol). The vessel was sealed and heated to 130 ° C for 2 h. The vessel was cooled to rt, diluted with MeOH and filtered. Concentrate the filtrate and pass SiO2 Purification by flash chromatography to produceAE-1 . At -10 ° CAE-1 (660 mg, 4.12 mmol) of Br in Br in EtOH (15 mL)2 (658 mg, 4.12 mmol). The reaction was stirred at rt for 3 h. Add NH3 The MeOH solution (2N, 1 mL) was neutralized. Concentrate the mixture and pass SiO2 Purification by flash chromatography to produceIntermediate AE . MS (ES+): m/z 240.9 [M+H]+ .method 7 : Intermediate AF Synthesis Stirring in a closed container at 80 ° CAF-1 (100 g, 561 mmol), EtI (131 g, 842 mmol) and TBAB (18 g, 56 mmol) in H2 A mixture of O (200 mL), acetone (150 mL) and toluene (150 mL) for 18 h. Dispense the mixture in H2 Between O and EtOAc. The organic layer was dried and concentrated. By SiO2 Purification of the residue by flash chromatography to produceAF-2 . MakeAF-2 (200 g, 1.09 mol), NBS (425.02 g, 2.39 mol) and AIBN (17.82 g, 108.54 mmol) in CCl4 The mixture in (1.40 L) was refluxed for 18 h. Dispense the mixture in H2 Between O and DCM. Dry (Na2 SO4 Organic layer, decanted and concentrated to produceAF-3 . At 0 °CAF- 3 (333 g, 974 mmol) and DIEA (129 g, 1 mol) in ACN (500 mL) were added dropwise in ACN (150 mL)AF-4 (138 g, 1 mol). The mixture was stirred for 5 h and then concentrated. The resulting residue is crystallized from MeOH to giveAF-5 . Will be at -78 ° CAF-5 (50 g, 190 mmol) in MeOH (200 mL) was added to NH3 In MeOH solution (2N, 800 mL). The reaction mixture was stirred at rt for 18 h then concentrated. The residue obtained from crystallization from EtOAc was providedAF-6 . Stirring at rtAF-6 (50 g, 250 mmol) in HCl in MeOH (1N, 250 mL) for 12 h then concentrated to give HCl saltIntermediate A F . MS (ES+): m/z 200.4 [M+H]+ .method 8 : Intermediate AG Synthesis At N2 Next, stir at rtAG-1 (8.0 g, 43.96 mmol), K2 CO3 (7.88 g, 57.1 mmol) and a mixture of sodium thiomethoxide (4.06 g, 48.3 mmol) in NMP (60.0 mL) for 18 h. Pour the reaction mixture into H2 O and filter. With H2 O wash the solid and dry it under vacuum to produceAG-2 . toAG-2 (6.0 g, 36.6 mmol) KMnO was added dropwise to a suspension of AcOH (2.63 g, 43.8 mmol)4 (5.78 g, 36.6 mmol) in H2 Solution in O (20.0 mL). The reaction mixture was stirred at rt for 15 h. The mixture was diluted with water and extracted with EtOAc. Dry (Na2 SO4 The organic layer was decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceAG-3 . In H2 Stir at rt (50 psi)AG-3 (3.3 g, 16.8 mmol) and Pd/C (500 mg, 10% on carbon catalyst) in MeOH (30 mL) for 8 h. Use N2 Purge the vessel, filter and concentrate the filtrate to produceAG-4 . toAG-4 (2.5 g, 12.5 mmol) EtOAc (2N, 20.0 mL). Stir the solution for 5 h at rt and then filter it to produceIntermediate AG . MS (ES+): m/z 201.2 [M+H]+ .method 9 : Intermediate AH Synthesis At N2 Next, stir at rtAH-1 (113 g, 0.62 mol), K2 CO3 (171 g, 1.24 mol) and a mixture of sodium ethanethiolate (67 g, 0.80 mol) in DMF (2 L) for 18 h. With H2 The mixture was diluted with EtOAc and extracted with EtOAc. Dry (Na2 SO4 The organic layer was decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceAH-2 . In H2 Stir at rt (50 psi)AH-2 (20.0 g, 0.12 mol), RaNi (40 g), Boc2 A solution of O (31.7 g, 0.14 mol) and TEA (24.5 g, 0.24 mol) in THF (600 mL) for 12 h. The mixture was filtered and the filtrate was concentrated under reduced pressure. By SiO2 The resulting residue was purified by flash chromatography to give AH-3. At -10 ° CAH- 3 (65 g, 0.24 mol) KMnO was added dropwise to a suspension in AcOH (200 mL)4 (45.8 g, 0.29 mL) solution in water (500 mL). After the addition was complete, the reaction mixture was stirred at rt for 30 min. With H2 O dilute the mixture and add aqueous Na2 CO3 Basify to ~pH 8 and extract with EtOAc. Dry (Na2 SO4 The combined organic layers were decanted and concentrated. Purifying the resulting residue by crystallization to produceAH-4 . Compound at rtAH-4 (46.5 g, 0.15 mol) MeOH (300 mL) EtOAc. The mixture was concentrated under reduced pressure. Purifying the resulting residue by crystallization to produceIntermediate AH . MS (ES+): m/z 202.1 [M+H]+ .method 10 : Intermediate AI Synthesis Stirring at 100 ° CAC (2 g, 9.4 mmol),AI-1 (4.8 g, 18.8 mmol), KOAc (2.8 g, 28.2 mmol) and Pd(dppf)Cl2 (1.15 g, 0.15 mmol) a suspension in 1,4-dioxane (40 mL) for 18 h. After cooling to rt, the~~~~~~~~ Dry (Na2 SO4 The combined organic phases were decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceAI . MS (ES+): m/z 262.2 [M+H]+ .method 11 : Intermediate AJ Synthesis toQQ (509 mg, 1.1 mmol) MeOH (4N, 1.1 mL, EtOAc. The reaction mixture was stirred at rt for 18 h. The mixture was concentrated under reduced pressure. The resulting residue was triturated with diethyl ether and filtered to giveIntermediate AJ-1 . toAJ-1 (200 mg, 0.55 mmol) TEA (0.77 mL, 5.51 mmol) was added to a solution in DCM (3 mL).AJ-2 (175 mg, 1.10 mmol). The reaction mixture was stirred at rt EtOAc (EtOAc) Dry (Na2 SO4 The organic layer was decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceIntermediate AJ . MS (ES+): m/z 485.0 [M+H]+ .method 12 : Intermediate AK Synthesis toAK-1 (2.00 g, 13.1 mmol) Add Boc to a solution in THF (25 mL)2 O (3.45 mL, 15.0 mmol) and TEA (3.64 mL, 26.1 mmol). Stir the reaction mixture at rt for 18 h and then with H2 O diluted and extracted with EtOAc. Concentrating the organic layer to produceAK-2 . toAK-2 (3.3 g, 13.1 mmol) slowly added H in a solution of AcOH (10 mL)2 O2 (1.37 mL, 13.7 mmol). Stir the reaction mixture at rt for 3 h and then with saturated Na2 SO3 (aq) Stop using 1N NaOH(aq) neutralize. The mixture was extracted with EtOAc and concentrated to giveAK-3 . toAK- 3 (1.0 g, 3.7 mmol), MgO (600 mg, 14.9 mmol), trifluoroacetamide (839 mg, 7.4 mmol) and Rh(II) acetate dimer (115 mg, 0.26 mmol) in DCM (10 mL) (Diethylphosphonioiodo)benzene (1.79 g, 5.6 mmol) was added to the mixture. The mixture was stirred at rt for 18 h and then concentrated under reduced pressure. The resulting residue was dissolved in MeOH, filtered over a pad of Celite and K was added2 CO3 (2.55 g, 18.6 mmol). The mixture was stirred at rt for 18 h and concentrated under reduced pressure. By SiO2 Purification of the resulting residue by flash chromatography to produceAK-4 . CompoundAK-4 (585 mg, 2.1 mmol) HCl solution (4N, 2 mL) in dioxane was added to a stirred solution in DCM (2 mL). The reaction mixture was stirred at rt for 15 h and then concentrated under reduced pressure to giveIntermediate AK . MS (ES+): m/z 185.0 [M+H]+ .method 13 : Intermediate AL Synthesis toAL-1 (500 mg, 2.18 mmol) in DIA (0.46 mL, 2.61 mmol), Boc2 O (1.02 g, 4.68 mmol) followed by DMAP (13.3 mg, 0.11 mmol). The reaction mixture was stirred at rt for 2.5 h. The reaction mixture was concentrated and the residue was diluted with EtOAc.2 O and brine cleaning, via Na2 SO4 Dry, filter and concentrate. By SiO2 Purification of the residue by flash chromatography to produceAL-2 . willAL-2 (250 mg, 0.85 mmol), Pd2 (dba)3 (39 mg, 0.043 mmol), Xanphos (41 mg, 0.071 mmol), Josiphos (13 mg, 0.024 mmol), and a mixture of TEA (0.83 mL, 0.97 mmol) in toluene (17 mL) were degassed and heated to 115 °C And keep it for 1 h. The reaction mixture was then cooled to rt and EtOAc (0.076 mL, &lt The reaction mixture was heated to 115 ° C for 3 h. Concentrate the reaction mixture and pass SiO2 Purification of the residue by flash chromatography to produceAL-3 . toAL-3 (200 mg, 0.71 mmol) A solution of potassium persulfate (961 mg, 1.56 mmol) in water (7 mL). The reaction mixture was stirred at rt for 18 h. Concentrate the mixture and then use H2 O diluted and extracted twice with DCM. Combine organics and wash with brine, Na2 SO4 Dry, filter and concentrate to produceAL-4 . toAL-4 (206 mg, 0.67 mmol) HCl (4N, 1.68 mL, 6.73 mmol) in dioxane. The reaction mixture was stirred at rt for 2 h. Concentrating the reaction mixture to produce a salt of HClAL . MS (ES+): m/z 207.1 [M+H]+ .method 14 : Intermediate AM Synthesis At 0 °CAM-1 (1 g, 7.80 mmol) <RTI ID=0.0>(1 </RTI> </RTI> The reaction mixture was warmed to rt and stirred overnight. The reaction mixture was then concentrated, diluted with water and then extracted with EtOAc. Then use saturated aq NaHCO3 (2X), H2 O (2X) and brine were washed with organic layer over MgSO4 Dry, filter and concentrate. By SiO2 Purification of the residue by flash chromatography to produceAM-2 . At 0 °CAM-2 (1 g, 3.81 mmol) dropwise in Br in THF (20 mL)2 (0.30 mL, 5.91 mmol). The reaction mixture was warmed to rt and stirred overnight. The reaction mixture was diluted with water and then extracted with EtOAc. Then use saturated aq NaHCO3 (2X), water (2X) and brine to wash the organic layer with MgSO4 Dry, filter and concentrate. By SiO2 Purification of the residue by flash chromatography to produceAM-3 . Similar toIntermediate AL-3 Way of synthesisAM-4 . Similar toIntermediate AL-4 Way of synthesisAM- 5 . toAM-5 (146 mg, 0.41 mmol) 10% Pd/C (150 mg) in EtOH (10 mL) and then in H2 The mixture was stirred at rt for 18 h under an atmosphere. The reaction mixture was filtered through Celite and washed with EtOAc. The filtrate was concentrated, then HBr was added in acetic acid (1.5 mL, 33%). The mixture was stirred at rt for 2.5 h and then filtered to give the HCl salt.AM . MS (ES+): m/z 221.1 [M+H]+ .method 15 : Intermediate AN Synthesis toAN-1 (6 g, 3.99 mmol) Add N to the solution in EtOH (60 mL)2 H4 Hydrate (31.1 ml). The mixture was heated to reflux and held for 45 min. The mixture was allowed to cool to rt and then concentrated. The residue was dissolved in diethylene glycol (20 mL) and EtOAc (EtOAc. The mixture was stirred at 120 ° C for 18 h. The mixture was cooled to rt, diluted with EtOAc and pH was adjusted to pH < 4 with 1 N HCl. Wash the organic layer with brine and pass Na2 SO4 Dry and concentrate. By SiO2 Purification of the residue by flash chromatography to produceAN-2 . At 0 °CAN-2 (1.3 g, 9.54 mmol) dropwise Br of Br in solution in DCM (20 mL)2 (1.53 g, 9.57 mmol). The mixture was stirred at rt for 12 h. Use aq NaHSO3 The mixture was stopped and extracted twice with DCM. Combine the organic layers and wash them with brine, via Na2 SO4 Dry and concentrate. By SiO2 Purification of the residue by flash chromatography to produceAN-3 . Similar toIntermediate AH-4 Way of synthesisAN-4 . toAN-4 (800 mg, 3.24 mmol) CuI (920 mg, 4.83 mmol) and CuCN (397 mg, 4.43 mmol) were added to a solution in NMP (10 mL). The microwave reaction was heated at 200 ° C for 3 h. Pour the mixture into H2 In O, it was extracted with EtOAc. Wash the organic layer with brine and pass Na2 SO4 Dry and concentrate. Purifying the residue by recrystallization to produceAN-5 . Similar toIntermediate AH-3 Way of synthesisAN-6 . Similar toIntermediate AH Way of synthesisAN . MS (ES+): m/z 198.0 [M+H]+ .method 16 : Intermediate AO Synthesis Add in portions to a solution of sodium 1-propionate (12.8 g, 130 mmol) in ACN (150 mL) kept below 20 °C.AG-1 (19.8 g, 108 mmol). The mixture was stirred at rt for EtOAc (EtOAc) (EtOAc) Dry (Na2 SO4 The combined organic phases were filtered and concentrated. By SiO2 Purification of the residue by flash chromatography to produceAO-1 . Keep below 10 ° CAO -1 (16.5 g, 83.0 mmol) KMnO was added dropwise to a stirred solution of AcOH (150 mL)4 (14.5 g, 92.0 mmol) in H2 Solution in O (150 mL). The reaction mixture was stirred for 30 min. Dilute the mixture with water by adding saturated aq Na2 CO3 Basify and extract with EtOAc. Concentrate the solution and purify the residue by SFC to produceAO-2 . In H2 Next, stir at rtAO-2 (7.80 g, 37.0 mmol) and a mixture of Ra Ni (8.00 g) in MeOH (100 mL) After filtration and concentration, the residue is purified by MPLC to produceAO-3 . SolidAO-3 (7.4 mL, 35.0 mmol) EtOAc (2 mL) Stir the solution for 5 h at rt and filter the solids to produceIntermediate AO .method 17 : Intermediate AP Synthesis Stirring at 110 ° CAP-1 (12.8 g, 130 mmol), sodium cyanosulfonate (53.1 g, 369 mmol) and a mixture of CuI (23.3 g, 123 mmol) in DMSO (150 mL) for 2 h. After cooling to rt, the solution was poured into water and extracted with EtOAc. Via Na2 SO4 The combined organic phases were dried, filtered and concentrated. The resulting residue is purified by MPLC to produceAP-2 . In H2 Stir at rt under the atmosphereAP-2 (10.3 g, 49 mmol), Ra Ni (25.0 g), Boc2 A mixture of O (16.2 g, 74 mmol) and EtOAc (10.0 g, EtOAc) After filtration and concentration, the residue is purified by MPLC to produceAP-3 . toAP-3 (6.90 g, 22 mmol) HCl in EtOAc (60 mL). Stir the solution for 3 h at rt and concentrate and recrystallize to produceIntermediate AP .method 18 : Intermediate AQ Synthesis toAG-1 (82.0 g, 448 mmol) Sodium butoxide (64.5 g) was added to a solution of ACN (1.0 L). The mixture was cooled to 0 ° C and sodium methanethiolate (172.5 g, 20% H) was added dropwise.2 O solution). The reaction mixture was then allowed to stir at rt for 16 h. Water (800 mL) was added and the mixture was extracted with DCM. The combined organic phases were washed with brine and dried (Na2 SO4 ) and concentrated. By SiO2 Purification of the residue by flash chromatography to produceAQ-1 . At 5 ° CAQ-1 (51.5 g, 343 mmol) KMnO was added dropwise to a suspension in AcOH (500 mL)4 (59.7 g, 36.6 mmol) in H2 Solution in O (500.0 mL). The reaction mixture was then stirred at rt for 1 h. The mixture was extracted with EtOAc using aq. NaHCO3 Cleaning, drying (Na2 SO4 ) and concentrated. Purifying the resulting residue by recrystallization to produceAQ-2 . toAQ-2 (15.0 g, 82 mmol) of Ra Ni (10.0 g), TEA (34.4 mL) and Boc in MeOH (200 mL)2 O (17.8 g). In H2 The mixture was stirred for 12 h at (50 psi). Use N2 The vessel was purged, filtered and the filtrate was concentrated. By SiO2 Purification of the residue by flash chromatography to produceAQ-3 . Stir in HCl in MeOH (500 mL) at rtAQ-3 (30.0 g, 105 mmol) solution for 12 h. Concentrate the mixture and recrystallize to produceIntermediate AQ . MS (ES+): m/z 187 [M+H]+ . Similar toIntermediate AQ Way of synthesisIntermediate AR andIntermediate AS (MS (ES+): m/z 202.1 [M+H]+ ). method 19 : Intermediate AT Synthesis At rtAT-1 (10.0 g, 55 mmol), N,N-dimethylethane-1,2-diamine (0.96 g, 11 mmol) and copper (II) triflate (1.98, 5 mmol) in DMSO ( Add in a mixture of 100 mL)AT -2 (8.27 g, 98 mmol). The mixture was then heated to 120 ° C for 30 min with H2 O was quenched and extracted with EtOAc. Dry the organic layer, concentrate and pass SiO2 Purification by flash chromatography to produceAT-3 . In H2 Stirring at rt (15 psi)AT-3 (32.3 g, 165 mmol) and Pd (3.50 g, 33 mmol) in NH4 Mixture of OH (30 mL) / EtOH (200 mL) for 15 h. Filter the mixture, concentrate and pass SiO2 Purification by flash chromatography to produceAT-4 . toAT-4 (17.5 g, 87 mmol) HCl in EtOH (100 mL) was added to a stirred solution in EtOH (100 mL). Stir the solution for 3 h at rt and then concentrate and recrystallize to produceIntermediate AT . MS (ES+): m/z 201 [M+H]+ .method 20 : Intermediate AU Synthesis toAU-1 (7.15 g, 26.5 mmol) Add Boc to a solution in THF (50 mL)2 O (6.70 mL, 29.2 mmol) and TEA (7.40 mL, 53.1 mmol). The reaction was allowed to stir at rt for 72 h. Concentrate the solution to produceAU-2 . willAU-2 (5.25 g, 15.8 mmol), sodium butoxide (1.82 g, 18.9 mmol), Pd (OAc)2 A mixture of (177 mg, 0.79 mmol) and 1,1'-bis(diisopropylphosphino)ferrocene (396 mg, 0.95 mmol) was added to a sealed vessel purged with argon. Dioxane (35 mL) was added and the mixture was stirred at rt for 1 h. Triisopropyldecanethiol (3.72 mL, 17.3 mmol) was added and the solution was heated to 100 ° C for 1 h. The reaction was then poured into EtOAc and water. Concentrate the organic layer and pass SiO2 Purification of the residue by flash chromatography to produceAU-3 . willAU-3 (2.50 g, 6.32 mmol) in THF (25 mL) was cooled to 0 &lt;0&gt;C and degassed with argon. Tetrabutylammonium bromide (2.12 g, 7.58 mmol) was then added and the solution was stirred at 0 °C for 1 h. Then bromoacetonitrile (660 uL, 9.48 mmol) was added and the solution was stirred at 0 ° C for 5 min. The solution was concentrated and partitioned between diethyl ether and water. Concentrating the organic layer to produceAU-4 , it can continue to be used without further processing. toAU-4 (1.80 g, 6.47 mmol) at ACN/H2 Sodium periodate (4.18 g, 19.5 mmol) was added to the solution in O (10 mL) followed by cerium (III) chloride (7.87 mg, 0.038 mmol). The reaction mixture was stirred at rt for 30 min and then concentrated. By SiO2 Purification of the residue by flash chromatography to produceAU-5 . toAU-5 (470 mg, 1.51 mmol) HCl solution in dioxane (2.00 mL, 8.00 mmol) was added to a stirred solution in DCM (3 mL). Stir the solution for 1 h at rt and concentrate to produceIntermediate AU . MS (ES+): m/z 211.1 [M+H]+ .method twenty one : Intermediate AV Synthesis Add to concentrated HCl (200 mL) at 0 °CAV-1 (20.0 g, 168 mmol) followed by aq NaNO2 (25.5 g in 25 mL H2 O)), maintain the internal temperature of <5 °C. Allow the solution to stir at 0 ° C for 15 min and then slowly add it to SO at 5 ° C2 (108 g) and CuCl (84 mg) in a mixture of AcOH (200 mL, > 5 eq.). The solution was stirred at 5 ° C for 90 min. The reaction mixture was extracted with DCM (2 x 500 mL) and dried (Na2 SO4 ) and use it directly in the next stepAV-2 Organic solution. At 0 °CAV-2 (20.0 g, 99 mmol) A solution of EtOAc (EtOAc) (EtOAc) The mixture is concentrated to dryness and passed through SiO2 Purification of the resulting residue by flash chromatography to produceAV-3 . toAV-3 (15.0 g, 82 mmol) of Ra Ni (10.0 g), TEA (34.4 mL) and Boc in MeOH (200 mL)2 O (17.8 g). In H2 The mixture was stirred at rt for 12 h at (50 psi). Use N2 The vessel was purged, filtered and the filtrate was concentrated. By SiO2 Purification of the residue by flash chromatography to give AV-4 . Stir in a solution of HCl in MeOH (500 mL) at rtAV-4 (30.0 g, 105 mmol) solution for 12 h. Concentrate and recrystallize the mixture to produceIntermediate AV . MS (ES+): m/z 188.1 [M+H]+ . Similar toIntermediate AV Way of synthesisIntermediate AW . method twenty two : Intermediate (S)-AX and (R)-AX Synthesis At -30 ° CAG-3 (2.40 g, 12 mmol) MeMgBr (30 mL) was added dropwise in THF (30 mL). After the addition, the mixture was stirred at rt for 4 h. By adding saturated aq NH4 The reaction mixture was quenched with EtOAc (EtOAc)EtOAc. Wash the organic phase with brine, via Na2 SO4 It was dried and concentrated under reduced pressure. By SiO2 Purification of the residue by flash chromatography to produceAX-1 . At 0 °CAX -1 (200 mg, 1.0 mmol) of NH in MeOH (2 mL)4 OAc (723 mg) and NaBH3 CN (41 mg). The mixture was stirred at rt for 16 h. The solvent was removed under reduced pressure, water (50 mL) was evaporated and evaporated. Via Na2 SO4 The organic phase was dried and concentrated. Purification of the residue by pre-TLC to produceAX -2 . Separated by SFCAX-2 To produce(S)-AX (67.9% ee) and(R)-AX (95.5% ee).method twenty three : Intermediate AY Synthesis toAY-1 (1.25 g, 5.49 mmol) NaOMe (2.37 g, 43.89 mmol). The mixture was stirred at rt for 1 h. The solution was filtered and concentrated. By SiO2 Purification of the residue by flash chromatography to produceIntermediate AY . MS (ES+): m/z 218.9 [M+H]+ .method twenty four : Intermediate AZ Synthesis Anhydrous isopropanol (360 uL, 4.71 mmol) was added to a solution of sodium hydride (342 mg, (60%), 8. The mixture was stirred at rt for 1 h. Then addAB-1 (1.00 g, 4.28 mmol) and the mixture was stirred for an additional 1 h then poured onto ice. The mixture was then extracted with EtOAc and concentrated. By SiO2 Purification of the residue by flash chromatography to produceIntermediate AZ . MS (ES+): m/z 258.8 [M+H]+ .method 25 : Intermediate BA Synthesis MakeBA-1 (1.00 g, 7.78 mmol) and Ni(dppe)Cl2 (82 mg, 0.16 mmol) in anhydrous Et2 The solution in O (5 mL) was cooled to -10 °C. Then, n-propyl magnesium bromide was added dropwise and the mixture was stirred at -10 °C for 2 h. Saturated NH4 The mixture was quenched with Cl, extracted with DCM and concentrated. RoughBA-2 Continue to use without further processing. At 0 °CBA-2 (1.0 g, 7.34 mmol) Add Br to a solution in EtOH (10 mL)2 (379 uL, 7.34 mmol). The reaction mixture was stirred at rt for 2 h. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceIntermediate BA . MS (ES+): m/z 217.4 [M+H]+ .method 26 : Intermediate BC Synthesis MakeBA-1 (1.00 g, 7.78 mmol) and Ni(dppe)Cl2 (82 mg, 0.16 mmol) in anhydrous Et2 The solution in O (5 mL) was cooled to -10 °C. A solution of isopropylmagnesium bromide (3.22 mL, 9.33 mmol) was added dropwise and the mixture was stirred at -10 °C for 1 h. Saturated NH4 The mixture was quenched with Cl, extracted with DCM and concentrated. RoughBC-1 Continue to use it in its own form. At 0 °CBC-1 (1.0 g, 7.34 mmol) Add Br to a solution in EtOH (10 mL)2 (378 uL, 7.34 mmol). The reaction mixture was stirred at rt for 2 h. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceIntermediate BC . MS (ES+): m/z 216.4 [M+H]+ .method 27 : Intermediate BD Synthesis MakeBA-1 (1.00 g, 7.78 mmol) and Ni(dppe)Cl2 (82 mg, 0.16 mmol) in anhydrous Et2 The solution in O (5 mL) was cooled to -10 °C. A solution of cyclopropylmagnesium bromide (1.36 g, 8.56 mmol) was added dropwise and the mixture was stirred at -10 °C for 2 h. Saturated aqueous NH4 The mixture was quenched with Cl, extracted with DCM and concentrated. RoughBD-1 Continue to use without further processing. At 0 °CBD-1 (1.0 g, 6.74 mmol) Add Br to a solution in EtOH (10 mL)2 (347 uL, 6.74 mmol). The reaction mixture was stirred at rt for 18 h. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceIntermediate BD . MS (ES+): m/z 229.2 [M+H]+ .method 28 : Intermediate BE Synthesis toBE-1 (40.0 g, 244 mmol) Add PPh to a solution in THF (800 mL)3 (98.0 g) and NCS (160.0 g). The reaction mixture was stirred at 80 ° C for 10 h. The mixture was then quenched with water and extracted with EtOAc. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceBE-2 . toBE-2 (3.00 g, 14.79 mmol) Add Pd (PPh) to a stirred solution of toluene and DMF3 )4 (600 mg), Pd(dppf)Cl2 (600 mg) and Na2 CO3 (6.27 g, 59.17 mmol). The mixture was stirred at 90 ° C for 5 h. The mixture was quenched with water and extracted with EtOAc. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceBE-3 . At -10 ° CBE-3 (860 mg, 5.0 mmol) added Br in a solution of EtOH (5 mL)2 (347 uL, 6.74 mmol). The reaction mixture was stirred at rt for 18 h. Concentrate the solution and pass SiO2 Purification of the residue by flash chromatography to produceIntermediate BE . MS (ES+): m/z 267 [M+H]+ .method 29 : Intermediate BF Synthesis Within 30 min at -78 ° CAB (6.00 g, 26.2 mmol) andBF -1 (7.86 mL, 34.1 mmol) n-Butyllithium (12.6 mL, 31.4 mmol) was added dropwise to a solution of toluene (60 mL) and THF (18 mL). The solution was stirred at -78 °C for 30 min and then slowly warmed to -20 °C. The solution was quenched with 1 N HCl (40 mL). The layers were then separated and the aqueous layer was adjusted to pH ~ 8 with 2M NaOH. The white solid began to precipitate and the mixture was allowed to cool in a cooler for 1 h. Filter solids to produceIntermediate BF . The aqueous layer was extracted with MeTHF and concentrated to give an additionalIntermediate BF . MS (ES+): m/z 195.1 [M+H]+ .Intermediate BG Synthesis A solution of n-butyllithium in hexane (2.5 M, 12.2 mL, 30.5 mmol) was added dropwise to a mixture of toluene (50 ml) and THF (12 ml) over 40 min.AC (5.00 g, 23.5 mmol) andBF-1 (7.04 mL, 30.5 mmol) in -78 ° C solution. The reaction mixture was stirred at -78 °C for 30 min, warmed to -20 ° C over 1 h and quenched with EtOAc (50 mL, 1 N). The resulting mixture was stirred at ambient temperature for 30 min, the phases were separated and the aqueous layer was neutralized to pH~7 with NaOH (4M). The turbid mixture was cooled to 0 ° C and the resulting precipitate was filtered to provideIntermediate BG . MS (ES+): m/z 178.9 [M+H]+ .method 30 : Intermediate BH Synthesis To 2-methylpropanal (5 g, 69.34 mmol) and NH4 To a mixture of Cl (7.42 g, 138.69 mmol) in water (50 mL), NaCN (4.08 g, 83.2 mmol). The mixture was stirred at rt for 18 h. The mixture was extracted with EtOAc (3x). Combine these organics with Na2 SO4 Dry and concentrate to produce a crude form that can be used without further processingIntermediate BH .method 31 : Intermediate BI Synthesis toBI-1 LiBr (1.86 g, 21.4 mmol) was added in one portion (20 mL, 104 mmol) and 2,2-dimethyloxirane (15 mL, 17 mmol). The reaction mixture was stirred at rt for 16 h. Additional 2,2-dimethyloxirane (2.0 mL, 23 mmol) was added and the mixture was heated at 60 °C for 2 h. The reaction mixture was quenched with water and then extracted twice with EtOAc. Combine organics and wash with brine, Na2 SO4 Dry, filter and concentrate to produceBI-2 . At -21 ° CBI-2 (2.0 g, 7.4 mmol) Deoxo-Fluor (1.51 mL, 8.17 mmol) was added to a solution in DCM (20 mL). After the addition, the reaction mixture was stirred at -21 ° C for 5 min, then saturated aq NaHCO3 Suspended until pH~8. The layers were separated and the aqueous layer was extracted with DCM. Saturated aq NaHCO3 Wash the combined organic matter through Na2 SO4 Dry, filter and concentrate to produceBI-3 . toBI-3 (1.5 g, 5.5 mmol) HCl solution (4N, 1.45 mL, 5.80 mmol). The reaction mixture was stirred at rt for 2 h, then filtered to giveBI-4 . At Endeavor (60°C, 400 psi)BI-4 A mixture of (500 mg, 1.62 mmol), 5% Pd/C (103 mg) and MeOH (3 mL) was hydrogenated for 5 h. The reaction mixture was filtered through Celite and washed with MeOH. Concentrate the filtrate to produce HCl saltIntermediate BI . MS (ES+): m/z 92.3 [M+H]+ .method 32 : Intermediate BJ Synthesis toBJ-1 (7.40 mL, 99.0 mmol) (R)-2-methyl-2-propanesulfinamide (10.0 g, 82.5 mmol), MgSO.4 (49.66 g, 412 mmol) and pyridinium p-toluenesulfonate (1.04 g, 4.13 mmol). The reaction mixture was allowed to stir at rt for 72 h. The reaction mixture is then filtered and passed through SiO2 Purification of the residue by flash chromatography to produceBJ-2 . toBJ-2 (9.72 g, 56.1 mmol) THF (6.27 g, 67.3 mmol) was added to a solution in THF (200 mL). The solution was degassed with argon and then allowed to cool to -55 °C. A solution of trifluoromethyltrimethylnonane (12.4 mL, 84.1 mmol) in THF (250 mL) was added dropwise with an additional funnel and the reaction was allowed to be stirred at -55 °C for 2 h. The reaction mixture is then allowed to slowly warm to -10 ° C and saturated aqueous NH4 Cl stopped. The aqueous layer was extracted with EtOAc and the combined organic layers were concentrated to dryBJ-3 . toBJ-3 (9.00 g, 37.0 mmol) MeOH (30 mL) EtOAc. The solution was allowed to stir at rt for 1 h. The reaction mixture was then concentrated to a half volume and diluted with diethyl ether until a white precipitate formed. Then filtering the solid to produceIntermediate BJ .method 33 : Intermediate BK Combination to maketoBK-1 (9.47 g, 113 mmol) (R)-2-methyl-2-propanesulfinamide (10.5 g, 86.6 mmol), MgSO.4 (52.1 g, 433 mmol) and pyridinium p-toluenesulfonate (1.09 g, 4.33 mmol). The reaction mixture was allowed to stir at rt for 18 h. The reaction mixture is then filtered and passed through SiO2 Purification of the residue by flash chromatography to produceBK-2 . At -50 ° CBK-2 (8.60 g, 45.9 mmol) Methylmagnesium bromide (36.0 mL, 108 mmol) was added to a solution in DCM (350 mL). The solution was stirred at -50 ° C for 3 h. The reaction was then allowed to warm to rt and stirred for 18 h. Saturated aqueous NH4 The solution was quenched with EtOAc (EtOAc) (EtOAc) Concentrate the organic layer to continue to use without further processingBK-3 . toBK-3 (5.00 g, 24.6 mmol) in MeOH (20 mL) EtOAc. The solution was allowed to stir at rt for 1 h. The reaction mixture is then concentrated and passed through SiO2 Purification of the residue by flash chromatography to produceIntermediate BK . Similar toIntermediate BK Way of synthesisIntermediate BL Similar toIntermediate AJ Way of synthesisIntermediate BM (MS (ES+): m/z 465.9 [M]+ ),BN (MS (ES+): m/z 467.0 [M]+ ),BO (MS (ES+): m/z 441.2 [M]+ ),BP (MS (ES+): m/z 452.9 [M]+ ),BQ (MS (ES+): m/z 441.0 [M]+ ),BR (MS (ES+): m/z 441.0 [M]+ ),BS (MS (ES+): m/z 467.0 [M]+ ). method 34 : Intermediate BT Synthesis Add (1S,2S)-2-amino-cyclopentanol to a stirred suspension of 2,4-dichloro-pyrimidin-5-ylamine (3.03 g, 18.1 mmol) in n-BuOH (40 mL) Hydrochloride (2.50 g, 17.2 mmol) and DIEA (9.20 mL, 51.8 mmol). The mixture was stirred at 130 ° C for 4 h. The reaction mixture was then concentrated under reduced pressure and the crude material was crystallBT-1 . toBT-1 (3.61 g, 15.5 mol) Add K to a stirred solution in acetone (200 mL)2 CO3 (5.34 g, 38.6 mmol) and chloro-s-oxy-ethyl acetate (1.94 mL, 17.0 mmol). The mixture was stirred at rt for 1 h. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The crude ketoester was dissolved in dry EtOH (50 mL), placed in a pressure-pressure flask and TEA (5.43 mL, 38.6 mmol). This was heated to 130 ° C for 1 h. The reaction mixture was concentrated under reduced pressure and evaporated in EtOAc EtOAc. Wash the organic layer with water (2 x 20 mL) and brine (20 mL) and dry (Na2 SO4 ), decanted and concentrated. The resulting residue was triturated to solid in EtOAc and heptane to giveBT-2 . toBT-2 (500 mg, 1.73 mmol) Dess-Martin periodinane (2.25 g, 5.20 mmol) was added to a mixture of DCM (100 mL) and the mixture was stirred at rt for 96 h. Saturated NaHCO3 (50 mL) wash the mixture and dry (Na2 SO4 The organic layer was concentrated under reduced pressure. The solid residue was suspended twice in DCM (50 mL), filtered and filtered. The resulting solid was resuspended in EtOAc (20 mL) and then applied. Filtering the solid product to produceBT-3 . At rtBT-3 (124 mg, 0.442 mmol) was added EtOAc (EtOAc) (EtOAc:EtOAc. The mixture was stirred at rt for 30 min while LCMS indicated the unreacted starting material. More grass chlorochloride (0.048 mL, 0.55 mmol) was added to the mixture and the mixture was stirred for additional 10 min. The reaction was concentrated at 35 ° C for 1 h under nitrogen flow and the residue was used directly.BT-4 . At rtBT-4 (132 mg, 0.442 mmol) andAG (105 mg, 0.442 mmol) <RTI ID=0.0></RTI> </RTI> <RTIgt; </RTI> <RTIgt; Water (50 mL) was added to the reaction mixture and the mixture was extracted with EtOAc (3.times. Combine organic layers and dry (Na2 SO4 ), decanted and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceIntermediate BT . MS (ES+): m/z 463.1 [M+H]+ .method 35 : Instance 9 Synthesis. IntermediateAB (27 mg, 0.12 mmol), bis(pinacol) diboron (30 mg, 0.12 mmol), potassium acetate (35 mg, 0.36 mmol) and [1,1'-bisdiphenylphosphinoferrocene] Palladium(II) dichloride (9 mg, 0.011 mmol) was combined in a solution of degassed toluene/DME/ethanol/water (3:2:2:1, 3 mL). The vessel was heated to 90 ° C in a microwave reactor for 20 min. In a separate container, the intermediateA (50 mg, 0.12 mmol), bis(pinacol) diboron (30 mg, 0.12 mmol), KOAc (35 mg, 0.36 mmol) and bis(di-t-butyl(4-dimethylaminophenyl) Phospho)dichloropalladium(II) (8 mg, 0.011 mmol) was combined in degassed 1,4-dioxane (3 mL). The reaction was heated to 90 ° C in a microwave reactor for 20 min. Combine the contents of the two containers and add Na2 CO3 (aq) (2M, 1 mL). The reaction was heated to 120 ° C in a microwave reactor for 30 min. The vessel was allowed to cool to rt and the contents were filtered and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceInstance 9 . MS (ES+): m/z 537.2 [M+H]+ .Instance 11 Synthesis. IntermediateAC (252 mg, 1.18 mmol), bis(pinacol) diboron (600 mg, 2.36 mmol), potassium acetate (348 mg, 2.36 mmol) and [1,1'-bisdiphenylphosphinoferrocene] Palladium(II) chloride (95 mg, 0.118 mmol) was combined in a solution of degassed toluene/DME/ethanol/water (3:2:2:1, 3 mL). The vessel was heated to 90 ° C in a microwave reactor for 20 min. In a separate container, the intermediateA (500 mg, 1.18 mmol), bis(pinacol) diboron (600 mg, 2.36 mmol), potassium acetate (348 mg, 2.36 mmol) and bis(di-t-butyl(4-dimethylamino)benzene Palladium(II) chloride (14 mg, 0.118 mmol) was combined in degassed 1,4-dioxane (3 mL). The reaction was heated to 90 ° C in a microwave reactor for 20 min. Combine the contents of the two containers and add Na2 CO3 (aq) (2M, 1 mL). The reaction was heated to 120 ° C in a microwave reactor for 30 min. The vessel was allowed to cool to rt and the contents were filtered and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceInstance 11 . MS (ES+): m/z 521.4 [M+H]+ .Instance 15 Synthesis. IntermediateAE (283 mg, 1.18 mmol), bis(pinacol) diboron (600 mg, 2.36 mmol), potassium acetate (348 mg, 3.54 mmol) and [1,1'-bisdiphenylphosphinoferrocene]- Palladium(II) chloride (95 mg, 0.12 mmol) was combined in a solution of degassed toluene/DME/ethanol/water (3:2:2:1, 3 mL). The vessel was heated to 90 ° C in a microwave reactor for 20 min. In a separate container, the intermediateA (500 mg, 1.18 mmol), bis(pinacol) diboron (600 mg, 2.36 mmol), potassium acetate (348 mg, 3.54 mmol) and bis(di-t-butyl(4-dimethylamino)benzene The phosphine dichloride palladium (II) (84 mg, 0.12 mmol) was combined in degassed 1,4-dioxane (3 mL). The reaction was heated to 90 ° C in a microwave reactor for 20 min. The contents of the two containers were combined and 2M sodium bicarbonate (1 mL) was added. The reaction was heated to 120 ° C in a microwave reactor for 30 min. The vessel was allowed to cool to rt and the contents were filtered and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceInstance 15 . MS (ES+): m/z 547.4 [M+H]+ .Instance 17 Synthesis. IntermediateAB (52 mg, 0.23 mmol), bis(pinacol) diboron (58 mg, 0.23 mmol), KOAc (67 mg, 0.23 mmol) and [1,1'-bisdiphenylphosphinoferrocene]- Palladium(II) chloride (18 mg, 0.23 mmol) was combined in a solution of degassed toluene/DME/ethanol/water (3:2:2:1, 3 mL). The vessel was heated to 90 ° C in a microwave reactor for 20 min. In a separate container, the intermediateG (100 mg, 0.23 mmol), bis(pinacol) diboron (58 mg, 0.23 mmol), KOAc (67 mg, 0.69 mmol) and bis(di-t-butyl(4-dimethylaminophenyl) Phosphine)dichloropalladium(II) (16 mg, 0.023 mmol) was combined in degassed 1,4-dioxane (3 mL). The reaction was heated to 90 ° C in a microwave reactor for 20 min. Combine the contents of the two containers and add Na2 CO3 (aq) (2M, 1 mL). The reaction was heated to 120 ° C in a microwave reactor for 30 min. The vessel was allowed to cool to rt and the contents were filtered and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceInstance 17 . MS (ES+): m/z 551.4 [M+H]+ .Instance 63 Synthesis. IntermediateAB (105 mg, 0.46 mmol), bis(pinacol) diboron (175 mg, 0.69 mmol), potassium acetate (67 mg, 0.69 mmol) and [1,1'-bisdiphenylphosphinoferrocene]- Palladium(II) chloride (18 mg, 0.045 mmol) was combined in a solution of degassed toluene/DME/ethanol/water (3:2:2:1, 3 mL). The vessel was heated to 90 ° C in a microwave reactor for 20 min. In a separate container, the intermediateB (100 mg, 0.23 mmol), bis(pinacol) diboron (175 mg, 0.69 mmol), KOAc (67 mg, 0.69 mmol) and bis(di-t-butyl(4-dimethylaminophenyl) Phosphine)dichloropalladium(II) (16 mg, 0.045 mmol) was combined in degassed 1,4-dioxane (3 mL). The reaction was heated to 90 ° C in a microwave reactor for 20 min. The contents of the two containers were combined and 2M sodium bicarbonate (1 mL) was added. The reaction was heated to 120 ° C in a microwave reactor for 30 min. The vessel was allowed to cool to rt and the contents were filtered and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceInstance 63 . MS (ES+): m/z 548.0 [M+H]+ .Instance 65 Synthesis. IntermediateAC (174 mg, 0.820 mmol), bis(pinacol) diboron (277 mg, 1.093 mmol), potassium acetate (161 mg, 1.64 mmol) and [1,1'-bisdiphenylphosphinoferrocene]- Palladium(II) chloride (43 mg, 0.055 mmol) was combined in a solution of degassed toluene/DME/ethanol/water (3:2:2:1, 3 mL). The vessel was heated to 90 ° C in a microwave reactor for 20 min. In a separate container, the intermediateX (247 mg, 0.547 mmol), bis(pinacol) diboron (277 mg, 0.820 mmol), potassium acetate (161 mg, 1.64 mmol) and bis(di-t-butyl(4-dimethylamino)benzene The phosphine dichloride palladium (II) (43 mg, 0.055 mmol) was combined in degassed 1,4-dioxane (3 mL). The reaction was heated to 90 ° C in a microwave reactor for 20 min. Combine the contents of the two containers and add Na2 CO3 (aq) (2M, 1 mL). The reaction was heated to 120 ° C in a microwave reactor for 30 min. The vessel was allowed to cool to rt and the contents were filtered and concentrated. By SiO2 Purification of the resulting residue by flash chromatography to produceInstance 65 . MS (ES+): m/z 550.0 [M+H]+ . The following compounds were produced in a similar manner: Examples1-8 , 10 , 12-14 , 16 , 18-62 , 64 , 66-92 , 129 .method 36 : Instance 93 Synthesis. Purge with argonAJ (100 mg, 0.21 mmol), intermediateAI (83.7 mg, 0.32 mmol), K3 PO4 (91 mg, 0.43 mmol) and Pd(dppf)Cl2 a mixture of (26 mg, 0.03 mmol) in 1,4-dioxane (2 mL) and then H2 O (0.25 mL). The mixture was stirred at 100 ° C for 18 h. The mixture was diluted with water (2 mL) and EtOAc (EtOAc. Dry (Na2 SO4 The combined organic phases were decanted and concentrated. The resulting residue was purified by reverse phase HPLC to giveInstance 93 . MS (ES+): m/z 584.0 [M+H]+ .Instance 136 Synthesis. Purge with argonNNN (3500 mg, 8.05 mmol), intermediateBG (2149 mg, 12.07 mmol), K3 PO4 (3417 mg, 16.09 mmol) and Pd(dppf)Cl2 a mixture of (986 mg, 1.21 mmol) in 1,4-dioxane (60 mL), and then H2 O (6 mL). The mixture was stirred at 100 ° C for 18 h. The mixture was diluted with water (2 mL) and EtOAc (EtOAc. Dry (Na2 SO4 The combined organic phases were decanted and concentrated. The resulting residue was purified by reverse phase HPLC to giveInstance 136 . MS (ES+): m/z 533.0 [M+H]+ .Instance 158 Synthesis Purge with argonMMM (3360 mg, 7.49 mmol), intermediateBG (2664 mg, 14.97 mmol), K3 PO4 (3177 mg, 14.97 mmol) and Pd(dppf)Cl2 a mixture of (916 mg, 1.12 mmol) in 1,4-dioxane (60 mL), and then H2 O (6 mL). The mixture was stirred at 100 ° C for 18 h. The mixture was diluted with water (2 mL) and EtOAc (EtOAc. Dry (Na2 SO4 The combined organic phases were decanted and concentrated. The resulting residue was purified by reverse phase HPLC to giveInstance 158 . MS (ES+): m/z 539.3 [M+H]+ . The following compounds were produced in a similar manner: Examples94-128 , 130-132 , 134 , 137-144 , 146-157 , 159-199 , 201-265 . method 37 : Instance 133 Synthesis: Purge with argonAC (5.39 g, 25.3 mmol), bis(pinacol) diboron (10.4 g, 40.5 mmol), potassium acetate (3.98 g, 40.5 mmol) and Pd(dppf)Cl2 DCM complex (0.83 g, 1.01 mmol) in DME/Tol/EtOH/H2 The mixture in O (10:6:3:1) was sealed and stirred at 80 ° C for 30 min. Add this mixture to the argon purgeBU-1 (Synthesized according to the procedure described in Step 1 and Step 2 of Method 1) (2.70 g, 10.1 mmol) and Pd(amphos)Cl2 (0.71 g, 1.01 mmol) of the mixture and the sealed mixture was heated to 110 ° C for 2 h. The mixture was then concentrated, diluted with EtOAc, filtered and concentrated. By SiO2 Purification of the crude product by flash chromatography to produceBU-2 . toBU-2 (856 mg, 2.35 mmol) Toluene (596 mg, 4.70 mmol) was added to a solution in DCM (15 ml), followed by 5 drops of DMF. The reaction was allowed to stir for 18 h. Then concentrate the reaction and residue yieldBU-3 It continues to be used in its own right. At rtBU-3 (150 mg, 0.36 mmol) DIEA (196 uL, 1.41 mmol) was added to a stirred solution of DMF. Added after 10 minutesBU-4 (84.1 mg, 0.42 mmol) and the reaction was stirred at rt for 10 min. The mixture is then concentrated and reversed by HPLC (NH4 CO3 Purification to produceInstance 133 . MS (ES+): m/z 509.1 [M+H]+ . Similar toInstance 133 Way of synthesisInstance 135 and 145 . method 38 : Instance 200 Synthesis: to216 (100 mg, 0.195 mmol) was added LiOH (28.0 mg, 1.. The reaction was stirred at rt for 16 h. The mixture was concentrated and dissolved in water, acidified to pH~5 with 1N HCl, filtered, washed with water and dried in a vacuum oven to give200 . MS (ES+): m/z 498.1 [M+H]+ .Biological activity The compounds of the present invention have activity as modulators of ROR gamma (orphan receptor gamma associated with retinoid receptors). Reporter gene analysis (RGA) Perform nuclear receptor transactivation assays to quantify the ability of test compounds to inhibit RORy transactivation of luciferase reporters. A similar analysis is described in Khan et al, Bioorganic & Medicinal Chemistry Letters 23 (2013), 532-536. The system used transiently transfected HEK 293 cells co-transfected with two plastids (pGL4.3, luc2P/GAL4UAS/Hygro and pBIND, Gal4DBD hRORC LBD1-3). The positive control was transiently transfected with two plastids and the negative control contained the pGL4.3 promoter sequence. The assays were combined in a 384 well plate in which transiently transfected cells and test compounds were incubated at different concentrations for 20-24 h. The next day, the assay disk was removed and equilibrated for 20-30 minutes at RT. Luciferase production was measured using the Bright-GloTM Luciferase Assay System. After adding the Bright GLO detection reagent, the plates were incubated at RT for 20 minutes. The discs are read on an Envision disc reader to measure the illuminating signal. The RLU signal is converted to a POC associated with the control well and the blank well. Cell seeding medium: RPMI 1640-Invitrogen #11875135), 2.5% FBS-Invitrogen # 26140, 1x Penicillin-Streptomycin-Gibco # 15140 Compound Dilution Buffer: 1X HBSS-Invitrogen #14025126 Plate: Greiner #781080-020 Bright Glo Fluorescent The enzyme assay system: Promega #E2620 melts the lysis buffer provided in the kit and adds 100 mL of the lysis buffer to the substrate. The following table presents the results obtained when testing the compounds of the invention in the above assays, which demonstrate their activity as ROR gamma modulators: Table II: Biological Activity Tables in Reporter Genetic Analysis Method of therapeutic use a biological property of a compound of the formula (I) according to the invention or a tautomer, a racemate, a mirror image isomer, a non-mironomer, a mixture thereof and all the salts of the above-mentioned forms, Both are suitable for the treatment of autoimmune and allergic diseases because they exhibit a good regulatory effect on RORγ. The invention accordingly relates to compounds of the general formula (I), and pharmaceutically acceptable salts thereof, and to all tautomers, racemates, mirror image isomers, non-mironomers, mixtures thereof, which are useful The invention relates to diseases and/or conditions in which the activity of a RORγ modulator is therapeutically beneficial, including but not limited to the treatment of autoimmune or allergic diseases. Such diseases which can be treated by the compounds of the invention include, for example, rheumatoid arthritis, psoriasis, systemic lupus erythematosus, lupus nephritis, systemic sclerosis, vasculitis, scleroderma, asthma, allergic rhinitis , allergic eczema, multiple sclerosis, juvenile rheumatoid arthritis, juvenile idiopathic arthritis, type I diabetes, Crohn's disease, ulcerative colitis, graft versus host disease, psoriatic arthritis , reactive arthritis, joint adhesion spondylitis, atherosclerosis, uveitis and non-radiative spondyloarthropathy. For the treatment of the above diseases and conditions, the therapeutically effective dose will generally be in the range of from about 0.01 mg to about 10 mg/kg body weight per dose of the compound of the invention; preferably, from about 0.1 mg to about 5 mg/kg body weight per dose . For example, when administered to a human of 70 kg, the dosage range is from about 0.7 mg to about 750 mg per dose of a compound of the invention, preferably from about 7.0 mg to about 350 mg per dose. A certain level of conventional dose optimization may be required to determine the optimal level and mode of administration. The active ingredient can be administered 1 to 6 times a day.General administration and pharmaceutical compositions When used as a medicament, the compounds of the invention are usually administered in the form of a pharmaceutical composition. Such compositions may be prepared using procedures well known in the art of pharmacy and generally comprise at least one compound of the invention and at least one pharmaceutically acceptable carrier. The compounds of the present invention may also be administered alone or in combination with an adjuvant which enhances the stability of the compounds of the present invention and facilitates the administration of pharmaceutical compositions containing such adjuvants in certain embodiments. Auxiliary treatments and the like are provided by enhanced solubility or dispersibility, enhanced antagonist activity. The compounds of the present invention may be used alone or in combination with other active substances of the present invention, and may be combined with other pharmacologically active substances as needed. In general, the compounds of the invention may be administered in a therapeutically effective amount or in a pharmaceutically effective amount, but may be administered in minor amounts for diagnostic or other purposes. The compounds of the present invention can be administered in pure form or in the form of a suitable pharmaceutical composition using any of the modes of administration of the acceptable pharmaceutical compositions. Thus, the administration can be, for example, oral, buccal (eg, sublingual), nasal, parenteral, topical, transdermal, vaginal or rectal, solid, semi-solid, lyophilized or Forms of liquid dosage forms such as, for example, lozenges, suppositories, pills, soft elastic gelatin capsules and hard gelatin capsules, powders, solutions, suspensions or mists or the like, preferably in unit dosage form suitable for simple administration of precise dosages . The pharmaceutical compositions will generally comprise a conventional pharmaceutical carrier or excipient and a compound of the invention as the active agent and, in addition, may comprise other pharmaceutical agents, pharmaceutical agents, carriers, adjuvants, diluents , a vehicle or a combination thereof. Such pharmaceutically acceptable excipients, carriers or additives are known to those skilled in the art and methods of making pharmaceutical compositions for use in various modes or administrations. The following literature confirms the current state of the art: Remington: The Science and Practice of Pharmacy, 20th edition, A. Gennaro (ed.), Lippincott Williams & Wilkins, 2000; Handbook of Pharmaceutical Additives, Michael & Irene Ash ( Ed., Gower, 1995; Handbook of Pharmaceutical Excipients, AH Kibbe (ed.), American Pharmaceutical Ass'n, 2000; HC Ansel and NG Popovish, Pharmaceutical Dosage Forms and Drug Delivery Systems, 5th edition, Lea and Febiger, 1990; Each of these documents is hereby incorporated by reference in its entirety to the extent of the extent of the present disclosure. As will be appreciated by those skilled in the art, the form of the compounds of the invention for use in a particular pharmaceutical formulation will be selected (e.g., a salt) to have suitable physical characteristics (e.g., water soluble) required to render the formulation effective. Sex). All patent or non-patent literature or literature cited in this application is incorporated herein by reference in its entirety.

Claims (33)

一種化合物，其係選自以下所組成之群，，，，，，，，，，及, 或其醫藥上可接受之鹽。a compound selected from the group consisting of , , , , , , , , ,and , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項1之化合物，其中該化合物係， 或其醫藥上可接受之鹽。The compound of claim 1, wherein the compound is , or a pharmaceutically acceptable salt thereof. 一種醫藥組合物，其包括如請求項2之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 2, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項3之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 3, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項4之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 4, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項5之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 5 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項6之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 6 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項7之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 7 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項8之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 8 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項9之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 9 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項10之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 10 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種醫藥組合物，其包括如請求項11之化合物或其醫藥上可接受之鹽，及醫藥上可接受之載劑。A pharmaceutical composition comprising a compound of claim 11 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 一種如請求項1之化合物或其醫藥上可接受之鹽之用途，其用於製造用於治療患者自體免疫疾病或過敏性疾病之藥劑。A use of the compound of claim 1 or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for treating an autoimmune disease or an allergic disease in a patient. 如請求項22之用途，其中該自體免疫疾病或過敏性疾病係選自類風濕性關節炎、牛皮癬、全身性紅斑狼瘡、狼瘡性腎炎、硬皮病、氣喘病、過敏性鼻炎、過敏性濕疹、多發性硬化症、幼年類風濕性關節炎、幼年特發性關節炎、I型糖尿病、炎症性腸病、移植物抗宿主病、牛皮癬性關節炎、反應性關節炎、關節黏連性脊椎炎、克羅恩氏病(Crohn's disease)、潰瘍性結腸炎、葡萄膜炎及非放射線脊椎關節病。The use of claim 22, wherein the autoimmune disease or allergic disease is selected from the group consisting of rheumatoid arthritis, psoriasis, systemic lupus erythematosus, lupus nephritis, scleroderma, asthma, allergic rhinitis, allergic Eczema, multiple sclerosis, juvenile rheumatoid arthritis, juvenile idiopathic arthritis, type I diabetes, inflammatory bowel disease, graft versus host disease, psoriatic arthritis, reactive arthritis, joint adhesion Spondylitis, Crohn's disease, ulcerative colitis, uveitis, and non-radiative spondyloarthropathy. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof. 如請求項23之用途，其中該化合物係， 或其醫藥上可接受之鹽。The use of claim 23, wherein the compound is , or a pharmaceutically acceptable salt thereof.
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