반응식
ClC1C=C2C(=CC=1)NC(C(N[C@@H]1CC3C(=CC=CC=3)NC1=O)=O)=C2.[C:25]([CH2:29][N:30]1[C:40]2[C:35](=[CH:36][CH:37]=[CH:38][CH:39]=2)[CH2:34][C@@H:33]([NH:41][C:42]([C:44]2[NH:45][C:46]3[C:51]([CH:52]=2)=[CH:50][C:49]([Cl:53])=[CH:48][CH:47]=3)=[O:43])[C:31]1=[O:32])([O:27][CH3:28])=[O:26].C(OC(N[C@@H]1CC2C(=CC=CC=2)NC1=O)=O)(C)(C)C>>[C:25]([CH2:29][N:30]1[C:40]2[C:35](=[CH:36][CH:37]=[CH:38][CH:39]=2)[CH2:34][C@H:33]([NH:41][C:42]([C:44]2[NH:45][C:46]3[C:51]([CH:52]=2)=[CH:50][C:49]([Cl:53])=[CH:48][CH:47]=3)=[O:43])[C:31]1=[O:32])([O:27][CH3:28])=[O:26]참가 물질
4
반응물 3
생성물 1
실험 절차
The title compound was prepared from (S)-3-t-butyloxycarbonylamino-3,4-dihydrocarbostyril (prepared in Example 5) by the procedures described for the preparation of (R)-1-carbomethoxymethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril (Example 7) from (R)-3-t-butyloxycarbonylamino-3,4-dihydrocarbostyril. HPLC/MS [M+H]+, 412.
출처 및 근거
- ORD 기록
- ord-f6b32ea6655540abb07919434d96aeb2
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07098235B2
연결된 노트
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