4-(2,4-Dimethylphenyl)piperazin-1-ylethylamine → HCID 16038501, compound

HRID 1984151Notes

Reaction equation

HRID 1984151 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.[C:18]1([N:24]2[C:28]([C:29]3[O:30][CH:31]=[CH:32][CH:33]=3)=[CH:27][C:26]([CH:34]=O)=[N:25]2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[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][NH:17][CH2:34][C:26]2[CH:27]=[C:28]([C:29]3[O:30][CH:31]=[CH:32][CH:33]=3)[N:24]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[N:25]=2)[CH2:11][CH2:10]1

Participants

3

Reactant 2

HCID 47424664-(2,4-Dimethylphenyl)piperazin-1-ylethylamineHCID 592816101-Phenyl-5-(2-furyl)pyrazole-3-carbaldehyde

Product 1

HCID 16038501HCID 16038501, compoundYield 92.2%

Procedure

Compound 30 was prepared using the same method as that of Example 1 except that 4-(2,4-dimethylphenyl)piperazin-1-ylethylamine and 1-phenyl-5-(2-furyl)pyrazole-3-carbaldehyde were used.

Sources & evidence

ORD record
ord-d6b42933b91349acb1ebe93cb7bcb1e6
Source dataset
uspto-grants-2009_06
Patent number
US07544686B2

Reaction notes

Loading…