4-(4-Chlorobenzhydryl)piperazin-1-ylethylamine → HCID 68974051, compound

HRID 1984198Notes

Reaction equation

HRID 1984198 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.[C:24]1([N:30]2[C:34]([C:35]3[O:36][CH:37]=[CH:38][CH:39]=3)=[CH:33][C:32]([CH:40]=O)=[N:31]2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[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][CH2:40][C:32]3[CH:33]=[C:34]([C:35]4[O:36][CH:37]=[CH:38][CH:39]=4)[N:30]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[N:31]=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 592816101-Phenyl-5-(2-furyl)pyrazole-3-carbaldehyde

Product 1

HCID 68974051HCID 68974051, compoundYield 62%

Procedure

Compound 97 was prepared using the same method as that of Example 1 except that 4-(4-chlorobenzhydryl)piperazin-1-ylethylamine and 1-phenyl-5-(2-furyl)pyrazole-3-carbaldehyde were used.

Sources & evidence

ORD record
ord-ef0d16f675ff4ea4bb3ea913107c79ed
Source dataset
uspto-grants-2009_06
Patent number
US07544686B2

Reaction notes

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