1-(3-chlorobenzyl)-1H-1,2,4-triazol-3-amine → [1-(3-Chloro-benzyl)-1H-[1,2,4]triazol-3-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine

HRID 2063698Notes

Reaction equation

HRID 2063698 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[C:11]([CH3:13])[N:10]=[CH:9]2)=[C:4]([O:14][CH3:15])[CH:3]=1.[Cl:16][C:17]1[CH:18]=[C:19]([CH:27]=[CH:28][CH:29]=1)[CH2:20][N:21]1[CH:25]=[N:24][C:23]([NH2:26])=[N:22]1>>[Cl:16][C:17]1[CH:18]=[C:19]([CH:27]=[CH:28][CH:29]=1)[CH2:20][N:21]1[CH:25]=[N:24][C:23]([NH:26][C:2]2[CH:7]=[CH:6][C:5]([N:8]3[CH:12]=[C:11]([CH3:13])[N:10]=[CH:9]3)=[C:4]([O:14][CH3:15])[CH:3]=2)=[N:22]1

Participants

3

Reactant 2

HCID 70193361-(3-chlorobenzyl)-1H-1,2,4-triazol-3-amineHCID 534156611-(4-bromo-2-methoxyphenyl)-4-methyl-1H-imidazole

Product 1

HCID 46216603[1-(3-Chloro-benzyl)-1H-[1,2,4]triazol-3-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine

Procedure

Prepared in analogy to example 1b) starting with 1-(4-bromo-2-methoxy-phenyl)-4-methyl-1H-imidazole (WO2009076352) and 1-(3-chloro-benzyl)-1H-[1,2,4]triazol-3-ylamine from example 7a). The title compound was obtained as a slightly yellow solid (Yield=13%). MS ISP (m/e): 395.2 (100) [(M+H)+].

Workup

  1. customPrepared in analogy to example 1b)

Sources & evidence

ORD record
ord-1ab3a5d920144872b60b81c885eb2f72
Source dataset
uspto-grants-2012_10
Patent number
US08288403B2

Reaction notes

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