HCID 7019333, compound → HCID 46214069, compound

HRID 2063703Notes

Reaction equation

HRID 2063703 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.[CH3:16][C:17]1[CH:29]=[CH:28][C:20]([CH2:21][N:22]2[CH:26]=[N:25][C:24]([NH2:27])=[N:23]2)=[CH:19][CH:18]=1>>[CH3:15][O:14][C:4]1[CH:3]=[C:2]([NH:27][C:24]2[N:25]=[CH:26][N:22]([CH2:21][C:20]3[CH:28]=[CH:29][C:17]([CH3:16])=[CH:18][CH:19]=3)[N:23]=2)[CH:7]=[CH:6][C:5]=1[N:8]1[CH:12]=[C:11]([CH3:13])[N:10]=[CH:9]1

Participants

3

Reactant 2

HCID 7019333HCID 7019333, compoundHCID 534156611-(4-bromo-2-methoxyphenyl)-4-methyl-1H-imidazole

Product 1

HCID 46214069HCID 46214069, compound

Procedure

Prepared in analogy to example 43 starting with 1-(4-bromo-2-methoxy-phenyl)-4-methyl-1H-imidazole and 1-(4-methyl-benzyl)-1H-[1,2,4]triazol-3-ylamine. The title compound was obtained as a light yellow solid (Yield=60%). MS ISP (m/e): 375.4 (100) [(M+H)+].

Sources & evidence

ORD record
ord-fda91037ba90454ea8ab09d6269ef80d
Source dataset
uspto-grants-2012_10
Patent number
US08288403B2

Reaction notes

Loading…