4-Bromobenzaldehyde → HCID 178508585, compound

HRID 1396803Notes

Reaction equation

HRID 1396803 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([N:8]2[CH2:13][CH2:12][N:11]([C:14](=[O:24])[CH2:15][O:16][C:17]3[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=3)[CH2:10][CH2:9]2)[C:5]([NH2:25])=[C:4]([NH2:26])[N:3]=1.[Br:27][C:28]1[CH:35]=[CH:34][C:31]([CH:32]=O)=[CH:30][CH:29]=1>>[NH2:1][C:2]1[N:3]=[C:4]2[C:5]([N:25]=[C:32]([C:31]3[CH:34]=[CH:35][C:28]([Br:27])=[CH:29][CH:30]=3)[NH:26]2)=[C:6]([N:8]2[CH2:9][CH2:10][N:11]([C:14](=[O:24])[CH2:15][O:16][C:17]3[CH:18]=[CH:19][C:20]([Cl:23])=[CH:21][CH:22]=3)[CH2:12][CH2:13]2)[N:7]=1

Participants

3

Reactant 2

HCID 707414-BromobenzaldehydeHCID 66758721HCID 66758721, compound

Product 1

HCID 178508585HCID 178508585, compoundYield 74%

Procedure

This compound was synthesized from 2,5,6-triamino-4-[4-(4-chlorophenoxyacetyl)piperazin-1-yl]pyrimidine and 4-bromobenzaldehyde in 74% yield.

Sources & evidence

ORD record
ord-16bb623f50ed4b96a98ae5f7cfde2a45
Source dataset
uspto-grants-2014_12
Patent number
US08901132B2

Reaction notes

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