• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】44787

【品名】tert-butyl (6S)-6-([2-[3-[[(2-iodobenzyl)sulfonyl]amino]-6-methyl-2-oxo-1(2H)-pyridinyl]acetyl]amino)-8-methyl-7-oxo-3,9-dioxa-2,8-diazadec-1-animidoylcarbamate

【CA登记号】

【 分 子 式 】C27H38IN7O9S

【 分 子 量 】763.61097

【元素组成】C 42.47% H 5.02% I 16.62% N 12.84% O 18.86% S 4.2%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

Synthetic pathway for obtaining EN 292685: Treatment of amino acid (I) with CbzOSu affords the protected amino acid (II), which is further protected by means of Boc2O to yield derivative (III). Condensation of amino acid (III) with N,O-dimethyl hydroxylamine by means of BOP and DIEA provides hydroxamic ester (IV), which is then subjected to hydrogenolysis over Pd/C in CHCl3 for selective deprotection, furnishing compound (V). Coupling of (V) to intermediate (VI) affords derivative (VII), which is then coupled to lithium derivative (VIII) to give protected compound (IX). Finally, the Boc group of (IX) is removed by treatment with TFA.

1 Soll, R.M.; Lu, T.; Tomczuk, B.E.; Spurlino, J.; Pan, W.; Bone, R.; Green, D.W.; Heteroaryl keto thrombin inhibitors: Design and synthesis. 220th ACS Natl Meet (Aug 20 2000, Washington DC) 2000, Abst MEDI 285.
2 Tumczuk, B.E.; Pan, W.; Soll, R.M.; Lu, T. (3-Dimensional Pharmaceuticals, Inc.); Heteroaryl protease inhibitors and diagnostic imaging agents. WO 0104117 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 44766 (2S)-2-amino-4-([[amino(imino)methyl]amino]oxy)butyric acid C5H12N4O3 详情 详情
(II) 44767 5-[4-[(5-methoxy-3-methyl-3H-imidazo[4,5-b]pyridin-2-yl)methoxy]benzyl]-3-trityl-1,3-thiazolidine-2,4-dione C38H32N4O4S 详情 详情
(III) 44775 (11S)-11-[[(benzyloxy)carbonyl]amino]-6-imino-2,2-dimethyl-4-oxo-3,8-dioxa-5,7-diazadodecan-12-oic acid C18H26N4O7 详情 详情
(IV) 44776 benzyl (1S)-6-imino-1-[[methoxy(methyl)amino]carbonyl]-10,10-dimethyl-8-oxo-4,9-dioxa-5,7-diazaundec-1-ylcarbamate C20H31N5O7 详情 详情
(V) 44785 tert-butyl (6S)-6-amino-8-methyl-7-oxo-3,9-dioxa-2,8-diazadec-1-animidoylcarbamate C12H25N5O5 详情 详情
(VI) 44786 2-[3-[[(2-iodobenzyl)sulfonyl]amino]-6-methyl-2-oxo-1(2H)-pyridinyl]acetic acid C15H15IN2O5S 详情 详情
(VII) 44787 tert-butyl (6S)-6-([2-[3-[[(2-iodobenzyl)sulfonyl]amino]-6-methyl-2-oxo-1(2H)-pyridinyl]acetyl]amino)-8-methyl-7-oxo-3,9-dioxa-2,8-diazadec-1-animidoylcarbamate C27H38IN7O9S 详情 详情
(VIII) 23162 1,3-thiazol-2-yllithium C3H2LiNS 详情 详情
(IX) 44788 tert-butyl imino([[(3S)-3-([2-[3-[[(2-iodobenzyl)sulfonyl]amino]-6-methyl-2-oxo-1(2H)-pyridinyl]acetyl]amino)-4-oxo-4-(1,2lambda(5),3-thiadiazol-2-yl)butyl]oxy]amino)methylcarbamate C27H35IN8O8S2 详情 详情
Extended Information