反応式
[NH2:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1.Cl[C:14]1[N:18]([CH2:19][C:20]2[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=2)[C:17]2[CH:27]=[CH:28][CH:29]=[CH:30][C:16]=2[N:15]=1>ClC(Cl)Cl>[F:26][C:23]1[CH:22]=[CH:21][C:20]([CH2:19][N:18]2[C:17]3[CH:27]=[CH:28][CH:29]=[CH:30][C:16]=3[N:15]=[C:14]2[NH:1][CH:2]2[CH2:3][CH2:4][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:6][CH2:7]2)=[CH:25][CH:24]=1参加物
反応条件
- 温度
- 120 °C
実験手順
A mixture of 9.8 parts of ethyl 4-amino-1-piperidinecarboxylate and 15 parts of 2-chloro-1-(4-fluorophenylmethyl)-1H-benzimidazole was heated to 120° C. The mixture was stirred at 120° C. during 43 hours. After cooling, 100 parts of trichloromethane were added and the whole was thouroughly stirred. The mixture was washed with water. The aqueous layer was separated and the organic mixture was filtered and evaporated. The collected solid material was dissolved in 100 parts of water and subsequently 100 parts of 20% sodium hydroxide solution were added. The precipitate was filtered and dried in vacuo at 50° C., yielding 12.1 parts (40.5%) of ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate; mp. 181° C. (compound 21).
後処理
- temperatureAfter cooling
- stirringthe whole was thouroughly stirred
- washThe mixture was washed with water
- customThe aqueous layer was separated
- filtrationthe organic mixture was filtered
- customevaporated
- dissolutionThe collected solid material was dissolved in 100 parts of water and subsequently 100 parts of 20% sodium hydroxide solution
- additionwere added
- filtrationThe precipitate was filtered
- customdried in vacuo at 50° C.
出典と根拠
- ORDレコード
- ord-4cf92ec6199f4e86980cc57881e512a1
- 出典データセット
- uspto-grants-1989_05
- 特許番号
- US04835161
関連ノート
読み込み中…