Ammonia → HCID 14518706、化合物

HRID 1723146ノート

反応式

HRID 1723146 の反応式
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

6

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

  1. customThe solvent was evaporated in vacuo
  2. customthe residue was purified by column chromatography over silica gel using
  3. additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
  4. customThe pure fractions were collected
  5. customthe eluent was evaporated in vacuo
  6. dissolutionThe residue was dissolved in 11 parts of 2,2'-oxybispropane
  7. filtrationThe crystallized product was filtered off
  8. 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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