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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164228Generated: November 1, 2026

Chloroacetaldehyde → HCID 13394199, compound

https://huagongshe.com/reaction/2164228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant2,6-Dimethoxy-4-aminopyrimidineHCID 76789—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
ProductHCID 13394199HCID 13394199—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.5 g (0.01 mole) of 4-amino-2,6-dimethoxypyrimidine and 3.0 g (0.015 mole) of 50% aqueous chloroacetaldehyde in 20 ml of water was heated at 80° C. for one hour, and was then cooled with an ice bath with concomitant neutralization with sodium bicarbonate. The solid which formed was separated by filtration and recrystallized from cyclohexane with treatment with decolorizing charcoal. White crystals of 5,7-dimethoxyimidazo[1,2-c]pyrimidine, m.p. 120°-121° C., were obtained. Analysis: Calculated for C8H9N3O2 : %C,53.6; %H,5.1; %N,23.5; Found: %C,53.5; %H,5.0; %N,23.6. The structural assignment was confirmed by infrared and nuclear magnetic resonance spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04503050
Source datasetuspto-grants-1985_03
ORD IDord-9e3a9064dfa24fe1bfe3e6f65c3ce100
Source noteuspto-grants-1985_03