Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107314Generated: October 31, 2026

4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester → HCID 135670794, compound

https://huagongshe.com/reaction/1107314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
ReactantHCID 12535786HCID 12535786—
SolventAcetonitrileHCID 6342—
ProductHCID 135670794HCID 135670794235.6%

Reaction Conditions

Temperature2 °C

Reaction Steps

2-Allyloxybenzamidine (from sodium, 0.22 g, in ethanol, 100 ml, and 2-allyloxybenzamidine hydrochloride, 2.00 g) was dissolved in acetonitrile (50 ml) and the resulting cooled (2° C.) solution was added to a cooled (2° C.) solution of ethyl 4-chloro-2-methylthio-5-pyrimidine carboxylate (2.19 g) in acetonitrile (50 ml). The temperature was allowed to rise and the reaction mixture was stirred overnight at ambient temperature. The volume of the reaction mixture was reduced by evaporation under reduced pressure to yield a solid (0.96 g) which was collected. More product (0.45 g) precipitated from the filtrate. The combined products were recrystallized twice from ethanol to yield the title compound, 340 mg, m.p. 205-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060477
Source datasetuspto-grants-2000_05
ORD IDord-98f59fac34134dd6868d28c1801bcf4a
Source noteuspto-grants-2000_05