2-[4-(4-Methoxyphenyl)piperazin-1-yl]ethanamine → HCID 16038637, compound

HRID 1984156Notes

Reaction equation

HRID 1984156 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][NH2:17])[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.[CH3:18][C:19]1[N:23]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[N:22]=[C:21]([CH:30]=O)[CH:20]=1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:10][CH2:11][N:12]([CH2:15][CH2:16][NH:17][CH2:30][C:21]3[CH:20]=[C:19]([CH3:18])[N:23]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[N:22]=3)[CH2:13][CH2:14]2)=[CH:7][CH:8]=1

Participants

3

Reactant 2

HCID 12561082-[4-(4-Methoxyphenyl)piperazin-1-yl]ethanamineHCID 141352365-Methyl-1-phenylpyrazole-3-carbaldehyde

Product 1

HCID 16038637HCID 16038637, compoundYield 22.1%

Procedure

Compound 37 was prepared using the same method as that of Example 1 except that 4-(4-methoxyphenyl)piperazin-1-ylethylamine and 5-methyl-1-phenylpyrazole-3-carbaldehyde were used.

Sources & evidence

ORD record
ord-86e455b50ad1429ea5df356f17b40dfe
Source dataset
uspto-grants-2009_06
Patent number
US07544686B2

Reaction notes

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