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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216992Generated: October 29, 2026

Aniline → HCID 21058688, compound

https://huagongshe.com/reaction/2216992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHCID 10054325HCID 10054325—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 21058688HCID 21058688—

Reaction Steps

A solution of 1-[2-(tert-butyl-diphenyl-silanyloxy)-1-(R)-methyl-ethyl]-7-chloro-3-(4-methoxy-phenyl)-4-(S)-methyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one (0.28 g; 0.45 mmol) (from Example 15a supra) and aniline (0.10 mL; 1.21 mmol) (Aldrich) in toluene (0.25 mL, dried over molecular sieves) was heated in an oil bath at 110° C. for 2 hours. The reaction was diluted with ethyl acetate and washed with water and brine, dried over anhydrous sodium sulfate and concentrated. The crude material was purified by flash chromatography (Biotage 40L; 40:60 ethyl acetate-hexanes) to give 1-[2-(tert-butyl-diphenyl-silanyloxy)-1-(R)-methyl-ethyl]-3-(4-methoxy-phenyl)-4-(S)-methyl-7-phenylamino-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one. (Yield 0.23 g; 73.0%). This material showed an e.e. of ˜95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112676B2
Source datasetuspto-grants-2006_09
ORD IDord-5d3210b25f854c2e86c752af0e2876bc
Source noteuspto-grants-2006_09