HCID 178509736, compound → HCID 178509737, compound

HRID 744713Notes

Reaction equation

HRID 744713 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]([C:17]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=2)=[CH:10][CH2:11][C:12]2[N:13]=[CH:14][NH:15][CH:16]=2)=[CH:5][CH:4]=1)#[N:2]>C(O)C>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]([C:17]2[CH:18]=[CH:19][C:20]([C:23]([F:25])([F:24])[F:26])=[CH:21][CH:22]=2)[CH2:10][CH2:11][C:12]2[N:13]=[CH:14][NH:15][CH:16]=2)=[CH:5][CH:4]=1)#[N:2]

Participants

3

Reactant 1

HCID 178509736HCID 178509736, compound

Product 1

HCID 178509737HCID 178509737, compound

Reagents, catalysts & solvents 1

HCID 702EthanolCatalyst

Procedure

4-[3-(4-cyanophenyl)-3-(4-trifiuoromethylphenyl)-2-propenyl]-1H-imidazole is hydrogenated in ethanol using 10% Pd/C as a catalyst to give the product.

Workup

  1. customto give the product

Sources & evidence

ORD record
ord-40df736679044428a6b4964cdbc234cd
Source dataset
uspto-grants-1996_09
Patent number
US05559141

Reaction notes

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