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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216995Generated: October 31, 2026

HCID 10364131, compound → HCID 10457220, compound

https://huagongshe.com/reaction/2216995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10364131HCID 10364131—
SolventTolueneHCID 1140—
SolventAnilineHCID 6115—
ProductHCID 10457220HCID 10457220—

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of crude 7-chloro-3-(4-methoxy-phenyl)-4-methyl-1-[1-(S)-phenyl-ethyl)-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one (308 mg, from 0.56 mmol) (from Example 17 supra) in aniline (0.195 mL) (Aldrich) was stirred at 100° C. for 3 hours. Reaction mixture was then cooled to room temperature, diluted with toluene (3 mL) and purified by column chromatography (silica gel) eluting with hexanes-ethyl acetate (1:1) to give 3-(4-methoxy-phenyl)-4-methyl-7-phenylamino-1-[1-(S)-phenyl-ethyl]-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one. (Yield 140 mg, 53.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112676B2
Source datasetuspto-grants-2006_09
ORD IDord-fef454b746dd4ff2a21a1ecf556f83cd
Source noteuspto-grants-2006_09