2,3,6-Trichlorobenzaldehyde → 6-[4-(2,3,6-Trichloro-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one

HRID 1993420Notes

Reaction equation

HRID 1993420 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[C:22]([Cl:23])=[CH:21][CH:20]=[C:19]([Cl:24])[C:16]=1[CH:17]=O>>[Cl:14][C:15]1[C:22]([Cl:23])=[CH:21][CH:20]=[C:19]([Cl:24])[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 207812,3,6-TrichlorobenzaldehydeHCID 1361025406-piperazin-1-yl-3H-pyrimidin-4-one2×

Product 1

HCID 1361025756-[4-(2,3,6-Trichloro-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one

Procedure

6-[4-(2,3,6-Trichloro-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 2,3,6-trichlorobenzaldehyde. Mass spectrum (ES) MH+=373.

Sources & evidence

ORD record
ord-e1c8b29fa14c43f596793f2f84b0ee1c
Source dataset
uspto-grants-2010_01
Patent number
US07652013B2

Reaction notes

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