2-Bromobenzaldehyde → HCID 136102553, compound

HRID 1993422Notes

Reaction equation

HRID 1993422 reaction equation
[N:1]1([C:7]2[N:12]=[CH:11][NH:10][C:9](=[O:13])[CH:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[Br:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH:17]=O>>[Br:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][N:4]1[CH2:5][CH2:6][N:1]([C:7]2[N:12]=[CH:11][NH:10][C:9](=[O:13])[CH:8]=2)[CH2:2][CH2:3]1

Participants

3

Reactant 2

HCID 811292-BromobenzaldehydeHCID 1361025406-piperazin-1-yl-3H-pyrimidin-4-one2×

Product 1

HCID 136102553HCID 136102553, compound

Procedure

6-[4-(2-Bromo-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one was prepared using Procedure A from 6-piperazin-1-yl-3H-pyrimidin-4-one (Intermediate 4) and 2-bromobenzaldehyde. Mass spectrum (ES) MH+=349.

Sources & evidence

ORD record
ord-29a10bf0ccd346f8aca4805a1554d996
Source dataset
uspto-grants-2010_01
Patent number
US07652013B2

Reaction notes

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