1-(3,4-dichlorophenyl)-3-methyl-1H-pyrazol-5-amine → 1-Acetyl-2[1-(3,4-dichlorophenyl)-3-methyl-5-pyrazolyl]amino-2-imidazoline

HRID 224850

Reaction equation

HRID 224850 reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[C:9]([Cl:14])[CH:8]=2)[N:5]=[C:4]([CH3:15])[CH:3]=1.[C:16]([N:19]1[CH2:23][C:22](=O)[N:21]=[CH:20]1)(=[O:18])[CH3:17]>>[C:16]([N:19]1[CH2:23][CH2:22][N:21]=[C:20]1[NH:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([Cl:13])=[C:9]([Cl:14])[CH:8]=2)[N:5]=[C:4]([CH3:15])[CH:3]=1)(=[O:18])[CH3:17]

Participants

3

Reactant 2

HCID 24021421-(3,4-dichlorophenyl)-3-methyl-1H-pyrazol-5-amineHCID 22350258N-acetyl-2-imidazolinone

Product 1

HCID 127638071-Acetyl-2[1-(3,4-dichlorophenyl)-3-methyl-5-pyrazolyl]amino-2-imidazoline

Procedure

5-Amino-3-methyl-1-(3,4-dichlorophenyl)pyrazole (16.6 g.) and 1-acetyl-2-imidazolinone (10.6 g.) were reacted as described in Example I to give 8.5 g. of product, mp 156°-157°.

Workup

  1. customto give 8.5 g

Sources & evidence

ORD record
ord-1cfbd6060ccb40619def53d8988aa76e
Source dataset
uspto-grants-1980_11
Patent number
US04234594

Linked notes

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