4-Hydroxybenzoic Acid → HCID 58933460, compound
Reaction equation
[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][CH:9]1[CH2:21][NH2:22])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:23][C:24]1[CH:32]=[CH:31][C:27]([C:28](O)=[O:29])=[CH:26][CH:25]=1>>[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][CH:9]1[CH2:21][NH:22][C:28](=[O:29])[C:27]1[CH:31]=[CH:32][C:24]([OH:23])=[CH:25][CH:26]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
The N-(1,4-Dibenzyl-piperazin-2-ylmethyl)-4-hydroxy-benzamide was prepared from C-(1,4-Dibenzyl-piperazin-2-yl)-methylamine and 4-hydroxybenzoic acid as described in EXAMPLE 1, Step 2.
Sources & evidence
- ORD record
- ord-022cb25889774b0da8ebb83df7dded7e
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07259157B2
Reaction notes
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