tert-butyl (E)-(2S,3S)-3-[(S)-2-(4-but-2-ynyloxy-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-2-hydroxy-2-propyl-10-(2-trimethylsilanyl-ethoxycarbonylamino)-dec-4-enoate → tert-butyl (E)-(2S,3S)-10-amino-3-[(S)-2-(4-but-2-ynyloxy-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-2-hydroxy-2-propyl-dec-4-enoate

HRID 1779229노트

반응식

HRID 1779229 반응식
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][C@H:13]([NH:18][C:19]([C@@H:21](/[CH:34]=[CH:35]/[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][NH:41]C(OCC[Si](C)(C)C)=O)[C@@:22]([OH:33])([CH2:30][CH2:31][CH3:32])[C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])=[O:20])[C:14]([O:16][CH3:17])=[O:15])=[CH:8][CH:7]=1)[C:2]#[C:3][CH3:4]>[N+](C)([O-])=O.[Cl-].[Zn+2].[Cl-]>[NH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]/[CH:35]=[CH:34]/[C@H:21]([C:19](=[O:20])[NH:18][C@H:13]([C:14]([O:16][CH3:17])=[O:15])[CH2:12][C:9]1[CH:10]=[CH:11][C:6]([O:5][CH2:1][C:2]#[C:3][CH3:4])=[CH:7][CH:8]=1)[C@@:22]([OH:33])([CH2:30][CH2:31][CH3:32])[C:23]([O:25][C:26]([CH3:28])([CH3:29])[CH3:27])=[O:24]

참가 물질

4

실험 절차

tert-Butyl (E)-(2S,3S)-3-[(S)-2-(4-but-2-ynyloxy-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-2-hydroxy-2-propyl-10-(2-trimethylsilanyl-ethoxycarbonylamino)-dec-4-enoate (298 mg, 0.415 mmol) was dissolved in nitromethane (1.5 mL), and zinc chloride (235 mg, 1.72 mmol) was then added at room temperature. The mixture was stirred for 4 hours, and then purified by preparative HPLC to obtain 192 mg (0.335 mmol, 81% yield) of tert-butyl (E)-(2S,3S)-10-amino-3-[(S)-2-(4-but-2-ynyloxy-phenyl)-1-methoxycarbonyl-ethylcarbamoyl]-2-hydroxy-2-propyl-dec-4-enoate.

후처리

  1. custompurified by preparative HPLC

출처 및 근거

ORD 기록
ord-77141676d9934a7ca5abc5c207f46185
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09266853B2

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