2-Chlorophenylhydrazine hydrochloride → methyl 1-(2-chlorophenyl)-5-(furan-2-yl)-1H-pyrazole-3-carboxylate
反応式
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6](=O)[CH2:7][C:8](=O)[C:9]([O:11][CH3:12])=[O:10].Cl.[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[NH:23][NH2:24]>CO>[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[N:23]1[C:6]([C:2]2[O:1][CH:5]=[CH:4][CH:3]=2)=[CH:7][C:8]([C:9]([O:11][CH3:12])=[O:10])=[N:24]1参加物
4
反応条件
- 温度
- 0 °C
実験手順
A stirred solution compound 5 (10.0 g, 50 mmol) and (2-chlorophenyl)hydrazine hydrochloride (10.0 g, 56 mmol) in methanol 80 mL was heated to reflux for 6 h. On cooling to 0° C., solid crashed out, filtered and washed with cold methanol to afford the title compound 6 (12.0 g, 80.0%) which was used for further reaction.
後処理
- temperatureto reflux for 6 h
- filtrationfiltered
- washwashed with cold methanol
出典と根拠
- ORDレコード
- ord-703c3e6eccc94c9688814495f9212eee
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987318B2
反応ノート
読み込み中…