5-Chloro-2-nitrobenzaldehyde → HCID 135879441, compound

HRID 1993432Notes

Reaction equation

HRID 1993432 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.[Cl:14][C:15]1[CH:16]=[CH:17][C:18]([N+:23]([O-:25])=[O:24])=[C:19]([CH:22]=1)[CH:20]=O>>[Cl:14][C:15]1[CH:16]=[CH:17][C:18]([N+:23]([O-:25])=[O:24])=[C:19]([CH:22]=1)[CH2:20][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 811235-Chloro-2-nitrobenzaldehydeHCID 1361025406-piperazin-1-yl-3H-pyrimidin-4-one2×

Product 1

HCID 135879441HCID 135879441, compound

Procedure

6-[4-(5-Chloro-2-nitro-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 5-chloro-2-nitrobenzaldehyde. Mass spectrum (ES) MH+=350.

Sources & evidence

ORD record
ord-e65a2e9d3c1c41b98a541b2d6c78d7ee
Source dataset
uspto-grants-2010_01
Patent number
US07652013B2

Reaction notes

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