1-Benzylpiperazine → HCID 15056318, compound

HRID 1085417Notes

Reaction equation

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

Participants

Reactant 2

HCID 759941-Benzylpiperazine

HCID 15680272HCID 15680272, compound

Product 1

HCID 15056318HCID 15056318, compound

Procedure

The title compound of Example 24 is converted to its acid chloride and is reacted with N benzylpiperazine by the method of Example 23 to give the title compound.

Sources & evidence

ORD record: ord-e8c0920fac94482594dfcea487251387
Source dataset: uspto-grants-1991_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05010080

Reaction notes

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