HCID 178432800, compound → HCID 178432791, compound

HRID 2297284Notes

Reaction equation

HRID 2297284 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:20])[C:10]([C:15]1[CH:19]=CN[N:16]=1)=[CH:11][N:12]([CH3:14])[CH3:13].ClC1C=C(Cl)C=CC=1C(=O)[CH2:30][C:31]1[N:32]=C(C)NC=1>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:20])[C:10]([C:15]1[N:16]=[C:31]([CH3:30])[NH:32][CH:19]=1)=[CH:11][N:12]([CH3:13])[CH3:14]

Participants

3

Reactant 2

HCID 178432800HCID 178432800, compoundHCID 178483574HCID 178483574, compound

Product 1

HCID 178432791HCID 178432791, compound

Procedure

Made using the same procedure as for 1-(2,4-dichlorophenyl)-3-(dimethylamino)-2-pyrazolylprop-2-en-1-one except that 1-(2,4-dichlorophenyl)-2-(2-methylimidazolyl)ethan-1-one (VI, 1.0 g, 3.7 mmol) was used. The crude residue was used without purification.

Workup

  1. customThe crude residue was used without purification

Sources & evidence

ORD record
ord-f2c2cb50f5b64cfebfa9cae2c556a788
Source dataset
uspto-grants-2002_12
Patent number
US06489344B1

Reaction notes

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