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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100480Generated: November 1, 2026

Potassium tert-butoxide → 6-chloro-2-[2-(2,5-difluoro-phenyl)-ethoxymethyl]-3H-pyrido[2,3-d]pyrimidin-4-one

https://huagongshe.com/reaction/2100480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2,5-dichloro-N-[2-[2-(2,5-difluorophenyl)ethoxy]ethanimidoyl]pyridine-3-carboxamideHCID 140520077—
SolventDimethyl SulfoxideHCID 679—
Product6-chloro-2-[2-(2,5-difluoro-phenyl)-ethoxymethyl]-3H-pyrido[2,3-d]pyrimidin-4-oneHCID 1358991809,200%

Reaction Conditions

Temperature50 °C

Reaction Steps

KOtBu (28 mg, 250 μmol) was added at ambient temperature to a solution of 2,5-dichloro-N-{2-[2-(2,5-difluoro-phenyl)-ethoxy]-1-imino-ethyl}-nicotinamide (97 mg, 250 μmol) in DMSO (1 ml). The solution was stirred for 1 h at 50° C., cooled to ambient temperature, KOtBu (28 mg, 250 μmol) was added and the reaction solution was stirred at 50° C. for 14 h. The mixture was poured onto isopropyl acetate/ice water 1/1. The layers were separated and the aqueous layer was extracted two times with isopropyl acetate. The combined extracts were washed three times with brine and dried over sodium sulfate. The solvent was removed under reduced pressure to leave a yellow solid which was recrystallized from dichloromethane/heptane to give 6-chloro-2-[2-(2,5-difluoro-phenyl)-ethoxymethyl]-3H-pyrido[2,3-d]pyrimidin-4-one (8 mg, 23 mmol; 9%) as yellow crystals. MS: m/e=352.3 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572801B2
Source datasetuspto-grants-2009_08
ORD IDord-cfbd32701e2846679bf359bcdc9a36ee
Source noteuspto-grants-2009_08