2-Methyl-1H-imidazole-4-carboxaldehyde → {3-[3-Benzyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}[(2-Methyl-1H-Imidazol-5-yl)Methyl]Amine

HRID 2104843

Reaction equation

HRID 2104843 reaction equation
[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:27])[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:29][C:30]1[NH:34][C:33]([CH:35]=O)=[CH:32][N:31]=1>>[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:35][C:33]3[NH:34][C:30]([CH3:29])=[N:31][CH:32]=3)[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:26])[F:27])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 27958782-Methyl-1H-imidazole-4-carboxaldehydeHCID 112342973-(3-Benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine

Product 1

HCID 66914091{3-[3-Benzyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}[(2-Methyl-1H-Imidazol-5-yl)Methyl]Amine

Procedure

This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 2-methyl-3H-imidazole-4-carbaldehyde. MS (ESI) m/z 473.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-5053e01422fb4857bb9754fb8fddc726
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Linked notes

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