Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858277Generated: November 1, 2026

HCID 22125146, compound → HCID 22125113, compound

https://huagongshe.com/reaction/1858277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22125146HCID 22125146—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
ProductHCID 22125113HCID 2212511399.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 250 mg (0.44 mmol) of 3-(2-bromophenyl)-3,4-dihydro-7-(methanesulfonyl)-1-[3-(methanesulfonyloxymethyl)phenyl]pyrimido[4,5-d]pyrimidin-2(1H)-one in 10 ml of dimethylformamide was treated with 111 mg (0.6 mmol) of potassium phthalimide and the mixture heated at 90° C. for 1 hour then cooled and evaporated. The residue was partitioned between 30 ml of dichloromethane and 30 ml of water. The organic phase was collected, dried over magnesium sulfate, filtered and evaporated to afford 270 mg (99%) of 3-(2-bromophenyl)-3,4-dihydro-7-(methanesulfonyl)-1-[3-(phthalimidomethyl)phenyl]pyrimido[4,5-d]pyrimidin-2(1H)-one as a white solid. [Mass spectrum (ESI) MH+ =618].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-7dbd74ee4df34987aebe76c117d5b4cb
Source noteuspto-grants-2000_11