tert-butyl 2-amino-4-[(1R)-1-({[(6S)-6-(5-chloro-2-methoxybenzyl)-7-oxo-6,7-dihydro-5H-imidazo[1,2-a][1,4]diazepin-8(9H)-yl]carbonyl}amino)propyl]benzoate → HCID 86672198, 화합물
반응식
[NH2:1][C:2]1[CH:14]=[C:13]([C@H:15]([NH:18][C:19]([N:21]2[C:27](=[O:28])[C@@H:26]([CH2:29][C:30]3[CH:35]=[C:34]([Cl:36])[CH:33]=[CH:32][C:31]=3[O:37][CH3:38])[CH2:25][N:24]3[CH:39]=[CH:40][N:41]=[C:23]3[CH2:22]2)=[O:20])[CH2:16][CH3:17])[CH:12]=[CH:11][C:3]=1[C:4]([O:6]C(C)(C)C)=[O:5]>Cl.C(O)(=O)C>[ClH:36].[NH2:1][C:2]1[CH:14]=[C:13]([C@H:15]([NH:18][C:19]([N:21]2[C:27](=[O:28])[C@@H:26]([CH2:29][C:30]3[CH:35]=[C:34]([Cl:36])[CH:33]=[CH:32][C:31]=3[O:37][CH3:38])[CH2:25][N:24]3[CH:39]=[CH:40][N:41]=[C:23]3[CH2:22]2)=[O:20])[CH2:16][CH3:17])[CH:12]=[CH:11][C:3]=1[C:4]([OH:6])=[O:5]참가 물질
4
실험 절차
The compound 89b obtained at Step (2) (27.2 mg) was dissolved in a 1M hydrochloric acid in acetic acid solution, then the mixture was stirred at room temperature for 3 hours. The precipitated solid was collected by filtration to obtain the title compound (17.8 mg).
후처리
- filtrationThe precipitated solid was collected by filtration
출처 및 근거
- ORD 기록
- ord-a229a169a6f341c9b1d674310c68c966
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08846660B2
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