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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280581Generated: October 31, 2026

Water → 3-(2-chlorophenyl)-7-methylthio-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one

https://huagongshe.com/reaction/1280581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexamethyldisilazaneHCID 13838—
Reactant[(2-Chlorophenyl)amino]-n-[5-(bromomethyl)-2-methylthiopyrimidin-4-yl]carboxamideHCID 23381125—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-(2-chlorophenyl)-7-methylthio-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 1842539570.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a suspension of [(2-chlorophenyl)amino]-N-[5-(bromomethyl)-2-methylthiopyrimidin-4-yl]carboxamide (1360 g, 3.62 mole) of in 10 L 1-methyl-2-pyrrolidinone was added 136 mL hexamethyldisilazane. The mixture was heated to an internal temperature of 105-115° C. for 1.5 hours. The mixture was then cooled to 30° C. and treated with 20L water. The mixture was then stirred at 5-8° C. for 2 hours and filtered. The filters were collected and washed sequentially with water and hexanes. The product was placed in a drying oven and heated under vacuum for 16 hours to give 780 g (70.1%) of 3-(2-chlorophenyl)-7-methylthio-3,4-dihydropyrimido[4,5-d] pyrimidin-2(1H)-one (sulfide 10.1) as an off-white solid. (M+1 308)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451804B1
Source datasetuspto-grants-2002_09
ORD IDord-d99bc270273a45a29faf55b47a54dc67
Source noteuspto-grants-2002_09