Reaction equation
[NH2:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:3]=1.[C:14]([N:17]1[CH2:21][C:20](=O)[N:19]=[CH:18]1)(=[O:16])[CH3:15]>>[C:14]([N:17]1[CH2:21][CH2:20][N:19]=[C:18]1[NH:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:3]=1)(=[O:16])[CH3:15]Participants
3
Procedure
5-Amino-1-methyl-3-phenylpyrazole (17.3 g.) and 1-acetyl-2-imidazolinone (15.4 g.) were reacted as described in Example I to give 14.0 g. product, mp 154°-155°.
Workup
- customto give 14.0 g
Sources & evidence
- ORD record
- ord-bd609a52f3504464aadfd00d47ab994b
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04226773
Linked notes
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