4-(4-Chlorobenzhydryl)piperazin-1-ylethylamine → 3-{2-[4-(4-Chlorobenzhydryl)piperazin-1-yl]ethyl}aminomethyl-1-phenyl-5-propylpyrazole

HRID 1984195Notes

Reaction equation

HRID 1984195 reaction equation
[Cl:1][C:2]1[CH:23]=[CH:22][C:5]([CH:6]([N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][NH2:21])[CH2:15][CH2:14]2)[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.[CH2:24]([C:27]1[N:31]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[N:30]=[C:29]([CH:38]=O)[CH:28]=1)[CH2:25][CH3:26]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:6]([N:13]2[CH2:14][CH2:15][N:16]([CH2:19][CH2:20][NH:21][CH2:38][C:29]3[CH:28]=[C:27]([CH2:24][CH2:25][CH3:26])[N:31]([C:32]4[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=4)[N:30]=3)[CH2:17][CH2:18]2)[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[CH:22][CH:23]=1

Participants

3

Reactant 2

HCID 142106204-(4-Chlorobenzhydryl)piperazin-1-ylethylamineHCID 862610985-Propyl-1-phenylpyrazole-3-carbaldehyde

Product 1

HCID 689750513-{2-[4-(4-Chlorobenzhydryl)piperazin-1-yl]ethyl}aminomethyl-1-phenyl-5-propylpyrazoleYield 95%

Procedure

Compound 94 was prepared using the same method as that of Example 1 except that 4-(4-chlorobenzhydryl)piperazin-1-ylethylamine and 5-propyl-1-phenylpyrazole-3-carbaldehyde were used.

Sources & evidence

ORD record
ord-d1935a99dd764c92a32f62de3def0e26
Source dataset
uspto-grants-2009_06
Patent number
US07544686B2

Reaction notes

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