1,3-Dimethyl-1H-pyrazol-5-amine → HCID 56985989, compound
Reaction equation
[NH2:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([CH3:8])[CH:3]=1.[C:9]([N:17]1[CH2:21][C:20](=O)[N:19]=[CH:18]1)(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[C:9]([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]([CH3:8])[CH:3]=1)(=[O:16])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
3
Procedure
5-amino-1,3-dimethylpyrazole (20.0 g.) and 1-benzoyl-2-imidazolinone (British Pat. No. 1,392,849) (28.4 g.) were reacted as described in Example I to give 22.02 g. product. mp 147°-149°
Workup
- custom1,392,849) (28.4 g.) were reacted
- customto give 22.02 g
Sources & evidence
- ORD record
- ord-32b2bc123c644494aa705d102697e6b2
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04234594
Reaction notes
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