N,N'-Dimethylthiourea → 3-Methyl-2-methylimino-7-(4-trifluoromethylphenyl)-2,3,8,8a-tetrahydroindeno[1,2-d]thiazol-3a-ol hydrobromide
반응식
[Br:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[C:11]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=2)[C:3]1=[O:21].[CH3:22][NH:23][C:24]([NH:26][CH3:27])=[S:25]>CC(C)=O>[BrH:1].[CH3:27][N:26]1[C:3]2([OH:21])[C:4]3[CH:5]=[CH:6][CH:7]=[C:8]([C:11]4[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=4)[C:9]=3[CH2:10][CH:2]2[S:25][C:24]1=[N:23][CH3:22].[CH3:27][N:26]1[C:3]2([OH:21])[C:4]3[CH:5]=[CH:6][CH:7]=[C:8]([C:11]4[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][CH:12]=4)[C:9]=3[CH2:10][CH:2]2[S:25][C:24]1=[N:23][CH3:22]참가 물질
5
반응물 2
생성물 2
시약·촉매·용매 1
실험 절차
426 mg (1.2 mmol) of 2-bromo-4-(4-trifluoromethylphenyl)-1-indanone and 130.2 mg (1.25 mmol) of N,N′-dimethylthiourea are dissolved in 10 ml of acetone and stirred at room temperature for 4 h. The precipitate is filtered off with suction, washed with acetone and dried in vacuo. The hydrobromide of 3-methyl-2-methylimino-7-(4-trifluoromethylphenyl)-2,3,8,8a-tetrahydroindeno[1,2-d]thiazol-3a-ol is obtained with a melting point of 202-204° C.
후처리
- filtrationThe precipitate is filtered off with suction
- washwashed with acetone
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-452c9e51b586441380e940f3ab95958f
- 출처 데이터셋
- uspto-grants-2001_09
- 특허 번호
- US06288094B1
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