2-(4-Phenylpiperazin-1-yl)ethan-1-amine → HCID 16039394, compound

HRID 1984128Notes

Reaction equation

HRID 1984128 reaction equation
[C:1]1([N:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][NH2:15])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:16][C:17]1[N:21]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:20]=[C:19]([CH:28]=O)[CH:18]=1>>[CH3:16][C:17]1[N:21]([C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)[N:20]=[C:19]([CH2:28][NH:15][CH2:14][CH2:13][N:10]2[CH2:9][CH2:8][N:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[CH2:12][CH2:11]2)[CH:18]=1

Participants

3

Reactant 2

HCID 47425032-(4-Phenylpiperazin-1-yl)ethan-1-amineHCID 141352365-Methyl-1-phenylpyrazole-3-carbaldehyde

Product 1

HCID 16039394HCID 16039394, compoundYield 46.9%

Procedure

Compound 2 was prepared using the same method as that of Example 1 except that 4-phenylpiperazin-1-ylethylamine and 5-methyl-1-phenylpyrazole-3-carbaldehyde were used.

Sources & evidence

ORD record
ord-a4014a1f03f6440187315da2392e39f3
Source dataset
uspto-grants-2009_06
Patent number
US07544686B2

Reaction notes

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