英文名称 (2S,4R)-1-Tert-Butyl 2-Methyl 4-((3-Chloro-7-Methoxyquinoxalin-2-yl)Oxy)Pyrrolidine-1,2-Dicarboxylate中文名称 格佐匹韦中间体2IUPAC名称 1-(tert-butyl) 2-methyl (2S,4R)-4-((3-chloro-7-methoxyquinoxalin-2-yl)oxy)pyrrolidine-1,2-dicarboxylate其它别名 1,2-Pyrrolidinedicarboxylic Acid, 4-[(3-Chloro-7-Methoxy-2-Quinoxalinyl)Oxy]-, 1-(1,1-Dimethylethyl) 2-Methyl Ester,(2S,4R)-; (2S,4R)-1-Tert-Butyl 2-Methyl 4-((3-Chloro-7-Methoxyquinoxalin-2-yl)Oxy)Pyrrolidine-1,2-Dicarboxylate; Grazoprevir Intermediate 2; 1-(Tert-Butyl) 2-Methyl (2S,4R)-4-((3-Chloro-7-Methoxyquinoxalin-2-yl)Oxy)Pyrrolidine-1,2-Dicarboxylate; (2S,4R)-4-[(3-Chloro-7-Methoxy-2-Quinoxalinyl)Oxy]-,1-(1,1-Dimethylethyl),- 1,2-Pyrrolidinedicarboxylic Acid 2-Methyl Ester; (2S,4R)-1-Tert-Butyl 2-Methyl 4-(2-Chloro-6-Methoxyquinoxalin-3-Yloxy)Pyrrolidine-1,2-DicarboxylateCAS编号 1206524-79-9 MFCD编号: MFCD26961025分子式: C20H24ClN3O6分子量: 437.88产品CID: 275524产品分类 有机原料 → 羧酸类化合物及衍生物
上下游产品 3-chloro-6-methoxyquinoxalin-2-ol 1-tert-butyl 2-methyl (2S,4S)-4-{[(4-bromo-phenyl)sulfonyl]oxy}-pyrrolidine-1,2-dicarboxylate 2,3-dihydroxy-6-methoxyquinoxaline 4-methoxyphenylene-1,2-diamine dihydr°Chloride methyl (4R)-4-[(3-chloro-7-methoxyquinoxalin-2-yl)oxy]-L-prolinate hydr°Chloride grazoprevir methyl (1aR,5S,8S,10R,22aR)-5-tert-butyl-14-methoxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methan°Cyclopropa[18,19][1,10,3,6]dioxa-diazacyclononadecino[11,12-b]quinoxaline-8-carboxylate (1aR,5S,8S,10R,22aR)-5-tert-butyl-14-methoxy-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradeca-hydro-8H-7,10-methan°Cyclopropa[18,19][1,10,3,6]dioxadiazacyclononadecino[11,12-b]quinoxaline-8-carboxylic acid hydrate 1-Tert-Butyl 2-Methyl (2S,4S)-4-{[(4-Bromo-Phenyl)Sulfonyl]Oxy}-Pyrrolidine-1,2-Dicarboxylate 以35%的收率获得格佐匹韦中间体2
参考文献:Hepatitis C Virus Ns3 Protease Inhibitors
标题:Hepatitis C Virus Ns3 Protease Inhibitors
摘要:本发明涉及一种具有式(i)的大环化合物,其可用作乙型肝炎病毒(hcv)ns3蛋白酶的抑制剂,以及它们的合成和用于治疗或预防hcv感染的用途.
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主要参考文献 参考标题:Development Of A Practical, Asymmetric Synthesis Of The Hepatitis C Virus Protease Inhibitor Mk-5172 作者:Jeffrey Kuethe,Yong-Li Zhong,Nobuyoshi Yasuda,Gregory Beutner,Katherine Linn,Mary Kim,Benjamin Marcune,Spencer Douglas Dreher,Guy Humphrey,Tao Pei |发布日期:2013.8.16 摘要:The Development Of A Practical, Asymmetric Synthesis Of The Hepatitis C Virus (Hcv) Protease Inhibitor Mk-5172 (1), An 18-Membered Macrocycle, Is Described.
合成参考文献 参考DOI号: 10.1021/acs.orglett.8b03173