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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634063Generated: October 30, 2026

4-Fluoroaniline → HCID 86585952, compound

https://huagongshe.com/reaction/1634063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanilineHCID 9731—
ReactantEthyl 4-chloro-2-methylthio-pyrimidine-5-carboxylateHCID 53249641—
SolventAcetonitrileHCID 6342—
ProductHCID 86585952HCID 8658595276.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 4-chloro-2-methylthiopyrimidine-5-carboxylate (Aldrich, 24 g, 103 mmol) in 250 mL of acetonitrile at room temperature was added 4-fluoroaniline (22.75 g, 205 mmol). After stirring for two days, the mixture was heated at 60° C. for four hours. The resulting solid was filtered and washed with EtOAc. The filtrate was concentrated, diluted in EtOAc (300 L), washed with brine, dried (MgSO4), filtered and concentrated to provide a crude product. The crude product was stirred with hexanes (400 mL) and then filtered to give 23 g of the ethyl 4-(4-fluorophenyl)amino-2-methylthiopyrimidine-5-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506749B2
Source datasetuspto-grants-2003_01
ORD IDord-09b88aac48634f05a38a88d3e0d1226f
Source noteuspto-grants-2003_01