Ethanol → HCID 86632604, 화합물
반응식
CO[C:3](=[O:26])[C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11]2[S:12][C:13]3[CH2:19][CH2:18][CH2:17][CH:16]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)[C:14]=3[N:15]=2)=[CH:6][CH:5]=1.O.[NH2:28][NH2:29].[CH2:30]([OH:32])C>>[CH3:30][O:32][C:9]1[CH:8]=[C:7]([NH:10][C:11]2[S:12][C:13]3[CH2:19][CH2:18][CH2:17][CH:16]([C:20]4[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=4)[C:14]=3[N:15]=2)[CH:6]=[CH:5][C:4]=1[C:3]([NH:28][NH2:29])=[O:26]참가 물질
4
반응 조건
- 온도
- 90 °C
실험 절차
To a suspension of 4-(4-phenyl-4,5,6,7-tetrahydro-benzothiazol-2-ylamino)-benzoic acid methyl ester (200 mg, 0.50 mmol) in ethanol (4 mL) was added hydrazine hydrate (0.6 mL) and the mixture was stirred for 7 hours at 90° C. The formed white precipitate was filtered off, washed with ethanol and dried to yield the title compound (130 mg, 65%) as a white solid which was used without further purification in the next step. mp 297-299° C. MS ISP (m/e): 393.5 (100) (M−H)−.
후처리
- filtrationThe formed white precipitate was filtered off
- washwashed with ethanol
- customdried
출처 및 근거
- ORD 기록
- ord-8cbb3755ff04456285979162ee660bda
- 출처 데이터셋
- uspto-grants-2011_04
- 특허 번호
- US07923450B2
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