Ethyl formate → 2-(2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-yl)ethylformamide
反応式
[NH:1]1[C:8]2[N:4]([N:5]=[CH:6][C:7]=2[CH2:9][CH2:10][NH2:11])[CH2:3][CH2:2]1.[CH:12](OCC)=[O:13]>>[NH:1]1[C:8]2[N:4]([N:5]=[CH:6][C:7]=2[CH2:9][CH2:10][NH:11][CH:12]=[O:13])[CH2:3][CH2:2]1参加物
3
実験手順
A suspension of 2-(2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-yl)ethylamine (155 mg) in ethyl formate (3 ml) was refluxed for 4.5 hours. After evaporation of the solvent in vacuo, the residue was triturated with ethyl acetate and dried in vacuo to give 2-(2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-yl)ethylformamide (165 mg) as a solid.
後処理
- temperaturewas refluxed for 4.5 hours
- customAfter evaporation of the solvent in vacuo
- customthe residue was triturated with ethyl acetate
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-20db1619b3a544cd8dc99178597891e5
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07179801B2
反応ノート
読み込み中…