Ethanol → HCID 86632604、化合物
反応式
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]参加物
4
反応条件
- 温度
- 90 °C
実験手順
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)−.
後処理
- filtrationThe formed white precipitate was filtered off
- washwashed with ethanol
- customdried
出典と根拠
- ORDレコード
- ord-8cbb3755ff04456285979162ee660bda
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07923450B2
反応ノート
読み込み中…