Ethyl formate → 2-(2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-yl)ethylformamide
Reaction equation
[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]1Participants
3
Procedure
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.
Workup
- temperaturewas refluxed for 4.5 hours
- customAfter evaporation of the solvent in vacuo
- customthe residue was triturated with ethyl acetate
- customdried in vacuo
Sources & evidence
- ORD record
- ord-20db1619b3a544cd8dc99178597891e5
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07179801B2
Reaction notes
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