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【结 构 式】

【分子编号】37768

【品名】tert-butyl (5R,9S)-15-amino-3-[(1S,2S)-1-[(benzyloxy)carbonyl]-2-[[tert-butyl(dimethyl)silyl]oxy]-3-(1,3-dioxan-2-yl)propyl]-9-(1-hydroxy-1-methylethyl)-10,13-dimethyl-4,8,11,14-tetraoxo-5-([[2-(trimethylsilyl)ethyl]sulfonyl]amino)-7-oxa-2,3,10,13-tetraazapentadecan-1-oate

【CA登记号】

【 分 子 式 】C45H80N6O15SSi2

【 分 子 量 】1033.39864

【元素组成】C 52.3% H 7.8% N 8.13% O 23.22% S 3.1% Si 5.44%

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:(XVII)

Deprotection of the benzyl ester of (XV) by catalytic hydrogenation over Pd/C afforded acid (XVI). On the other hand, deprotection of the Fmoc group of (XV) with diethylamine gave rise to amine (XVII). Coupling of both building blocks (XVI) and (XVII) was mediated by EDC and HOAt, providing the linear decadepsipeptide (XVIII).

1 Ledeboer, M.W.; Jin, Q.; Kume, M.; Searcey, M.; Boger, D.L.; Total synthesis and comparative evaluation of luzopeptin A - C and quinoxapeptin A - C. J Am Chem Soc 1999, 121, 49, 11375.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XV) 37766 tert-butyl (5R,9S)-3-[(1S,2S)-1-[(benzyloxy)carbonyl]-2-[[tert-butyl(dimethyl)silyl]oxy]-3-(1,3-dioxan-2-yl)propyl]-19-(9H-fluoren-9-yl)-9-(1-hydroxy-1-methylethyl)-10,13-dimethyl-4,8,11,14,17-pentaoxo-5-([[2-(trimethylsilyl)ethyl]sulfonyl]amino)-7,18-dioxa-2,3,10,13,16-pentaazanonadecan-1-oate C60H90N6O17SSi2 详情 详情
(XVI) 37767 (11S,15R,18S)-17-[(tert-butoxycarbonyl)azanyl]-18-[(1S)-1-[[tert-butyl(dimethyl)silyl]oxy]-2-(1,3-dioxan-2-yl)ethyl]-1-(9H-fluoren-9-yl)-11-(1-hydroxy-1-methylethyl)-7,10-dimethyl-3,6,9,12,16-pentaoxo-15-([[2-(trimethylsilyl)ethyl]sulfonyl]amino)-2,13-dioxa-4,7,10,17-tetraazanonadecan-19-oic acid C53H84N6O17SSi2 详情 详情
(XVII) 37768 tert-butyl (5R,9S)-15-amino-3-[(1S,2S)-1-[(benzyloxy)carbonyl]-2-[[tert-butyl(dimethyl)silyl]oxy]-3-(1,3-dioxan-2-yl)propyl]-9-(1-hydroxy-1-methylethyl)-10,13-dimethyl-4,8,11,14-tetraoxo-5-([[2-(trimethylsilyl)ethyl]sulfonyl]amino)-7-oxa-2,3,10,13-tetraazapentadecan-1-oate C45H80N6O15SSi2 详情 详情
(XVIII) 37769   C98H162N12O31S2Si4 详情 详情
Extended Information