4-(2,4-Dimethylphenyl)piperazin-1-ylethylamine → 5-(4-Cyclohexyl phenyl)-3-{2-[4-(2,4-dimethylphenyl)piperazin-1-yl]ethyl}aminomethyl-1-phenylpyrazole

HRID 1984154Notes

Reaction equation

HRID 1984154 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][NH2:17])[CH2:11][CH2:10]1.[CH:18]1([C:24]2[CH:29]=[CH:28][C:27]([C:30]3[N:34]([C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)[N:33]=[C:32]([CH:41]=O)[CH:31]=3)=[CH:26][CH:25]=2)[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]1>>[CH:18]1([C:24]2[CH:29]=[CH:28][C:27]([C:30]3[N:34]([C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)[N:33]=[C:32]([CH2:41][NH:17][CH2:16][CH2:15][N:12]4[CH2:13][CH2:14][N:9]([C:3]5[CH:4]=[CH:5][C:6]([CH3:8])=[CH:7][C:2]=5[CH3:1])[CH2:10][CH2:11]4)[CH:31]=3)=[CH:26][CH:25]=2)[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]1

Participants

3

Reactant 2

HCID 47424664-(2,4-Dimethylphenyl)piperazin-1-ylethylamineHCID 862611315-(4-Cyclohexylphenyl)-1-phenylpyrazole-3-carbaldehyde

Product 1

HCID 160385655-(4-Cyclohexyl phenyl)-3-{2-[4-(2,4-dimethylphenyl)piperazin-1-yl]ethyl}aminomethyl-1-phenylpyrazoleYield 52.8%

Procedure

Compound 34 was prepared using the same method as that of Example 1 except that 4-(2,4-dimethylphenyl)piperazin-1-ylethylamine and 5-(4-cyclohexyl phenyl)-1-phenyl pyrazole-3-carbaldehyde were used.

Sources & evidence

ORD record
ord-0ab0f75d792d4f0d9483e7c62c71ad67
Source dataset
uspto-grants-2009_06
Patent number
US07544686B2

Reaction notes

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