반응식
C(OC([N:8]1[C:12]2[CH:13]=[CH:14][C:15]([Cl:17])=[CH:16][C:11]=2[N:10]=[C:9]1[C:18]1[CH:23]=[C:22]([N:24]2[CH2:29][CH2:28][CH:27]([C:30]([O:32]CC)=[O:31])[CH2:26][CH2:25]2)[CH:21]=[CH:20][C:19]=1[F:35])=O)(C)(C)C>Cl>[ClH:17].[Cl:17][C:15]1[CH:14]=[CH:13][C:12]2[NH:8][C:9]([C:18]3[CH:23]=[C:22]([N:24]4[CH2:25][CH2:26][CH:27]([C:30]([OH:32])=[O:31])[CH2:28][CH2:29]4)[CH:21]=[CH:20][C:19]=3[F:35])=[N:10][C:11]=2[CH:16]=1참가 물질
3
반응 조건
- 온도
- 120 °C
실험 절차
Method 10—Step b A mixture of 5-Chloro-2-[5-(4-ethoxycarbonyl-piperidin-1-yl)-2-fluoro-phenyl]-benzoimidazole-1-carboxylic acid tert-butyl ester (0.30 g, 0.60 mmol) in 6N HCl (10 mL) was heated in microwave at 120° C. for 15 minutes, two cycles were needed. Solvent was removed under vacuum, then the solid was filtered and washed with diethyl ether and dried to obtain 0.17 g of the title compound (70%).
후처리
- customSolvent was removed under vacuum
- filtrationthe solid was filtered
- washwashed with diethyl ether
- customdried
출처 및 근거
- ORD 기록
- ord-f584e951ef744dbd88437a0f511dff0a
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08835648B2
연결된 노트
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