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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369961Generated: October 25, 2026

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

https://huagongshe.com/reaction/1369961

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 numberUS06579984B1
Source datasetuspto-grants-2003_06
ORD IDord-7a93166462b64cdebc1e56a9a6383143
Source noteuspto-grants-2003_06