Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611086Generated: October 25, 2026

Ethyl Acetate → Methyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/1611086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCyanamideHCID 9864—
ReactantHCID 178500902HCID 178500902—
SolventWaterHCID 962—
ProductMethyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylateHCID 104242488.4%

Reaction Steps

A suspension of 1.33 g of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate (5.00 mmol) in 4.20 g of 50% strength aqueous cyanamide solution (50.0 mmol) was heated to reflux. After 17 h, it was cooled to room temperature and treated with ethyl acetate (5 ml) and water (5 ml). The undissolved solid was filtered off. The organic phase was separated off and the aqueous phase was extracted with ethyl acetate (2×5 ml). The combined organic phases were dried over magnesium sulphate and concentrated in vacuo. The crude product (0.97 g) was purified by flash chromatography on silica gel (eluent: methylene chloride). 121.6 mg of methyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate were obtained in the form of a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984757B2
Source datasetuspto-grants-2006_01
ORD IDord-c418bd3b30284e4e82a77ef46b915cbe
Source noteuspto-grants-2006_01