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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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6-Nitroquinoxaline-2-carboxylic acid → (4S)-1-{(2S,3S)-3-[N2-(6-Nitro-2-quinoxalinecarbonyl)-L-asparaginyl]amino-2-hydroxy-4-phenylbutyryl}-4-chloro-N-t-butyl-L-prolinamide

HRID 1780265
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HRID 1780265 반응식
Cl.[NH2:2][C@H:3]([C:8]([NH:10][CH:11]([CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[CH:12]([OH:28])[C:13]([N:15]1[CH2:26][CH:25]([Cl:27])[CH2:24][C@H:16]1[C:17]([NH:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[O:14])=[O:9])[CH2:4][C:5](=[O:7])[NH2:6].[N+:36]([C:39]1[CH:40]=[C:41]2[C:46](=[CH:47][CH:48]=1)[N:45]=[C:44]([C:49](O)=[O:50])[CH:43]=[N:42]2)([O-:38])=[O:37]>>[N+:36]([C:39]1[CH:40]=[C:41]2[C:46](=[CH:47][CH:48]=1)[N:45]=[C:44]([C:49]([NH:2][C@H:3]([C:8]([NH:10][C@@H:11]([CH2:29][C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)[C@H:12]([OH:28])[C:13]([N:15]1[CH2:26][C@@H:25]([Cl:27])[CH2:24][C@H:16]1[C:17]([NH:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[O:14])=[O:9])[CH2:4][C:5](=[O:7])[NH2:6])=[O:50])[CH:43]=[N:42]2)([O-:38])=[O:37]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 190498156-Nitroquinoxaline-2-carboxylic acidHCID 677230331-[3-(L-asparaginyl)amino-2-hydroxy-4-phenylbutyryl]-4-chloro-N-t-butyl-L-prolinamide hydrochloride

생성물 1

HCID 86750833(4S)-1-{(2S,3S)-3-[N2-(6-Nitro-2-quinoxalinecarbonyl)-L-asparaginyl]amino-2-hydroxy-4-phenylbutyryl}-4-chloro-N-t-butyl-L-prolinamide수율 29.6%

실험 절차

Following a procedure similar to that described in Example 14, but using 490 mg (0.92 mmol) of 1-[3-(L-asparaginyl)amino-2-hydroxy-4-phenylbutyryl]-4-chloro-N-t-butyl-L-prolinamide hydrochloride and 220 mg (1.01 mmol) of 6-nitroquinoxaline-2-carboxylic acid (prepared as described in Preparation 22), 190 mg of the title compound were obtained as a pale yellow powder, melting at 153°-156° C.

출처 및 근거

ORD 기록
ord-ff77e9df036441839247aff78b65bb12
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05629406

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