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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993354Generated: November 1, 2026

Thiophenol → 2-Fluoro-4-(2-(phenylamino)pyrimidin-5-yl)phenol

https://huagongshe.com/reaction/1993354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(3-fluoro-4-methoxyphenyl)-N-phenylpyrimidin-2-amineHCID 57445393—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Fluoro-4-(2-(phenylamino)pyrimidin-5-yl)phenolHCID 57445394—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-(3-fluoro-4-methoxyphenyl)-N-phenylpyrimidin-2-amine (Step 2, 0.066 g, 0.22 mmol), thiophenol (0.20 g, 1.0 mmol), and K2CO3 (0.15 g, 1.1 mmol) in NMP (2 mL) was heated at 120° C. for 20 h. The mixture was cooled to RT and diluted with H2O (4 mL). After stirring for 10 min, the resulting suspension was filtered, and the solid was further washed with H2O. The solid was washed with hexanes to provide the title compound as a brown solid. MS (ESI pos. ion) m/z: 282. Calc'd for C16H12FN3O: 281.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652009B2
Source datasetuspto-grants-2010_01
ORD IDord-b925e905939943bda3fa52233e6c9381
Source noteuspto-grants-2010_01