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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216973Generated: October 30, 2026

(+/-)-1-[1-(2-Chloro-pyrimidin-5-yl)-ethyl]-1-(2-fluoro-4-methoxy-phenyl)-3-phenyl-urea → (+/-)-7-chloro-3-(2-fluoro-4-methoxy-phenyl)-4-methyl-1-phenyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one

https://huagongshe.com/reaction/2216973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-1-[1-(2-Chloro-pyrimidin-5-yl)-ethyl]-1-(2-fluoro-4-methoxy-phenyl)-3-phenyl-ureaHCID 21946011—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-7-chloro-3-(2-fluoro-4-methoxy-phenyl)-4-methyl-1-phenyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-oneHCID 10431009—

Reaction Steps

This urea was suspended in freshly distilled tetrahydrofuran (3 mL) and cooled in an ice-brine bath. Potassium tert-butoxide (1.0 M in tetrahydrofuran; 0.64 mL; 0.64 mmol) (Aldrich) was added dropwise to the suspension over 5 minutes. The solid went into solution as the potassium tert-butoxide was added. After stirring for an additional 15 minutes in the cold, the reaction mixture was filtered through a bed of silica gel (1.75 g), eluting with 1:1 ethyl acetate-hexanes and then ethyl acetate. Purification by flash chromatography (Biotage 40S; 40:60 to 50:50 ethyl acetate-hexanes) gave (±)-7-chloro-3-(2-fluoro-4-methoxy-phenyl)-4-methyl-1-phenyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one. (Yield 0.22 g; 38% overall for two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112676B2
Source datasetuspto-grants-2006_09
ORD IDord-735782dea91b404b8b94b4d7fa425fd8
Source noteuspto-grants-2006_09