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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476361Generated: October 30, 2026

Potassium Carbonate → N-[4-(4-amino-2,5-difluorophenoxy)-6-chloropyrimidin-2-yl]acetamide

https://huagongshe.com/reaction/476361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Amino-2,5-difluorophenolHCID 2778762—
ReactantN-(4,6-Dichloropyrimidin-2-yl)acetamideHCID 12611964—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-[4-(4-amino-2,5-difluorophenoxy)-6-chloropyrimidin-2-yl]acetamideHCID 8666287044%

Reaction Steps

A solution of 4-amino-2,5-difluoro-phenol (3.5 g, 24 mmol), N-(4,6-dichloro-pyrimidin-2-yl)-acetamide (5.30 g, 24 mmol) and potassium carbonate (3.4 g, 24 mmol) in DMF (100 mL) was stirred at 50° C. under nitrogen overnight. After cooling to room temperature the reaction mixture was suspended in water (300 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layers was washed with brine, dried over sodium sulfate and concentrated. The crude product was purified by silica gel chromatography (15%-20% ethyl acetate in petroleum ether) to give N-[4-(4-amino-2,5-difluoro-phenoxy)-6-chloro-pyrimidin-2-yl]-acetamide (3.3 g, 44% yield) as a white solid. 1HNMR (400 MHz, DMSO-d6): δ 10.72 (s, 1H), 7.20-7.24 (dd, J=11.2 Hz, J=7.6 Hz, 1H), 7.00 (s, 1H), 6.64 (dd, J=12.0 Hz, J=8.4 Hz, 1H), 5.48 (s, 2H), 2.03 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637672B2
Source datasetuspto-grants-2014_01
ORD IDord-dc9a2079720c431098d0573e8fa3522f
Source noteuspto-grants-2014_01