1-benzyl-3-methyl-1H-pyrazol-5-amine → 1-Acetyl-2-(1-benzyl-3-methyl-5-pyrazolyl)amino-2-imidazoline
Reaction equation
[NH2:1][C:2]1[N:6]([CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1.[C:15]([N:18]1[CH2:22][CH:21]=[N:20][C:19]1=O)(=[O:17])[CH3:16]>>[C:15]([N:18]1[CH2:22][CH2:21][N:20]=[C:19]1[NH:1][C:2]1[N:6]([CH2:7][C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1)(=[O:17])[CH3:16]Participants
3
Procedure
5-Amino-1-benzyl-3-methylpyrazole (J. Gen. Chem. USSR, 31, 2307, 1961) (17.0 g.) and 1-acetyl-3-imidazolinone (14.0 g.) were reacted as described in Example I to give 11.7 g. of product, mp 148°-149°.
Workup
- customto give 11.7 g
Sources & evidence
- ORD record
- ord-dc1e9310df5d407b83a81c4060c8bc84
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04234594
Reaction notes
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