HCID 19421997, compound → HCID 178509744, compound

HRID 744710Notes

Reaction equation

HRID 744710 reaction equation
Cl.C([N:9]1[C:13]([CH2:14][CH2:15][CH:16]=[C:17]([C:26]2[CH:31]=[CH:30][C:29]([C:32]#[N:33])=[CH:28][CH:27]=2)[C:18]2[CH:23]=[CH:22][C:21]([C:24]#[N:25])=[CH:20][CH:19]=2)=[CH:12][N:11]=[CH:10]1)C1C=CC=CC=1>C(O)C>[C:24]([C:21]1[CH:20]=[CH:19][C:18]([CH:17]([C:26]2[CH:27]=[CH:28][C:29]([C:32]#[N:33])=[CH:30][CH:31]=2)[CH2:16][CH2:15][CH2:14][C:13]2[N:9]=[CH:10][NH:11][CH:12]=2)=[CH:23][CH:22]=1)#[N:25]

Participants

3

Reactant 1

HCID 19421997HCID 19421997, compound

Product 1

HCID 178509744HCID 178509744, compound

Reagents, catalysts & solvents 1

HCID 702EthanolCatalyst

Procedure

1-benzyl-5-[4,4-bis(4-cyanophenyl)-3-butenyl]-1H-imidazole hydrochloride 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-54cdc60dbab74cffad142fcd5bcaa378
Source dataset
uspto-grants-1996_09
Patent number
US05559141

Reaction notes

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