Ammonia → HCID 14518706、化合物
反応式
N#N.C1(C[C:10]2[C:15]([CH2:16][N:17]3[CH:21]=[CH:20][N:19]=[CH:18]3)=[CH:14][CH:13]=[C:12]([NH2:22])[C:11]=2[NH2:23])CCCCC1.[F:24][C:25]([F:31])([F:30])[C:26](=N)OC.F[C:33](F)(F)[C:34](O)=O.N>CO>[CH:34]1([CH2:33][N:23]2[C:11]3[CH:10]=[C:15]([CH2:16][N:17]4[CH:21]=[CH:20][N:19]=[CH:18]4)[CH:14]=[CH:13][C:12]=3[N:22]=[C:26]2[C:25]([F:31])([F:30])[F:24])[CH2:14][CH2:15][CH2:10][CH2:11][CH2:12]1参加物
実験手順
A mixture of 2.75 parts of N2 -(cyclohexylmethyl)-4-(1H-imidazol-1-ylmethyl)-1,2-benzenediamine, 1.85 parts of methyl 2,2,2-trifluoroethanimidate, 40 parts of methanol and 2.3 parts of trifluoroacetic acid was stirred for 7 hours at room temperature. The reaction mixture was made alkaline with methanol, saturated with ammonia. The solvent was evaporated in vacuo and the residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated in vacuo. The residue was dissolved in 11 parts of 2,2'-oxybispropane. The crystallized product was filtered off and dried, yielding 1.9 parts (52.4%) of 1-(cyclohexylmethyl)-6-(1H-imidazol-1-ylmethyl)-2-(trifluoromethyl)-1H-benzimidazole; mp. 165.4° C. (compound 202).
後処理
- customThe solvent was evaporated in vacuo
- customthe residue was purified by column chromatography over silica gel using
- additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
- customThe pure fractions were collected
- customthe eluent was evaporated in vacuo
- dissolutionThe residue was dissolved in 11 parts of 2,2'-oxybispropane
- filtrationThe crystallized product was filtered off
- customdried
出典と根拠
- ORDレコード
- ord-c0b00f770d3d46c1b1acbb7d7c765b64
- 出典データセット
- uspto-grants-1989_08
- 特許番号
- US04859684
反応ノート
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