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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858234Generated: November 3, 2026

Phosgene → 3-(2,6-difluorophenyl)-7-methylthio-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one

https://huagongshe.com/reaction/1858234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-(2,6-Difluorophenyl)aminomethyl-4-methylamino-2-methylthiopyrimidineHCID 22125139—
SolventTetrahydrofuranHCID 8028—
Product3-(2,6-difluorophenyl)-7-methylthio-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 2212510387.4%

Reaction Steps

A stirred solution, cooled in ice, of 0.7 ml (1.3 mmol) of phosgene (20% in toluene) in 5 ml of tetrahydrofuran was treated dropwise with a solution of 210 mg (0.71 mmol) of 5-(2,6-difluorophenyl)aminomethyl-4-methylamino-2-methylthiopyrimidine and 0.2 ml (1.4 mmol) of triethylamine in 5 ml of tetrahydrofuran. The mixture was stirred for 1 hour. To the mixture were added 20 ml of tetrahydrofuran and 20 ml of saturated aqueous ammonium chloride solution and the phases were separated. The organic phase was dried over magnesium sulfate, filtered and evaporated to give 200 mg (87%) of 3-(2,6-difluorophenyl)-7-methylthio-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one as a white solid. [Mass spectrum (ESI) MH+ =323].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-b6a5992a81aa4f4a8fb11d36f3592c88
Source noteuspto-grants-2000_11