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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200541Generated: October 29, 2026

4-Chlorobenzaldehyde → 6-amino-5-(4-chlorobenzylamino)-3-methylpyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/2200541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSS-3364HCID 1201412—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-amino-5-(4-chlorobenzylamino)-3-methylpyrimidine-2,4(1H,3H)-dioneHCID 9040327142.9%

Reaction Steps

To a solution of 5,6-diamino-3-methylpyrimidine-2,4(1H,3H)-dione (0.8 g, 5.13 mmol) in water (10 mL) and acetic acid (0.5 mL) was added 4-chlorobenzaldehyde (0.72 g, 5.14 mmol), the mixture was stirred at room temperature for 5 h. The mixture was cooled to 0° C., sodium cyanoborohydride (0.3 g, 4.76 mmol) was added and the resulting mixture was stirred at room temperature overnight. The mixture was concentrated and filtered, and the filter cake was washed with methanol, dried in vacuo to give 6-amino-5-(4-chlorobenzylamino)-3-methylpyrimidine-2,4(1H,3H)-dione (0.6 g, 42.9% yield) as yellow solid. LCMS MH+ 281.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359359B2
Source datasetuspto-grants-2016_06
ORD IDord-326c75503d254cf799e33f299497d0a6
Source noteuspto-grants-2016_06