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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858179Generated: October 27, 2026

4-(2-(Diethylamino)ethoxy)aniline → HCID 22125070, compound

https://huagongshe.com/reaction/1858179

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(Diethylamino)ethoxy)anilineHCID 418932—
Reactant3-(2,6-dichlorophenyl)-7-methanesulfonyl-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 18425444—
ProductHCID 22125070HCID 221250709.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 2.55 g (6.6 mmol) of 3-(2,6-dichlorophenyl)-7-methanesulfonyl-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one and 7 g (34 mmol) of 4-[2-(diethylamino)ethoxy]-aniline was heated at 180° C. for 35 minutes and then cooled. The residue was chromatographed on silica gel using firstly 5% methanol in dichloromethane and then dichloromethane/methanol/acetic acid/water (240:24:3:2) for the elution. Product-containing fractions were combined and evaporated. The residue was evaporated with toluene and then dissolved in 150 ml of dichloromethane. The solution was washed with 100 ml of saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate and evaporated to give 1.18 g (35%) of crude product. Purification by crystallisation from cyclohexane/ethyl acetate gave 310 mg (9%) of pure 3-(2,6-dichlorophenyl)-7-[4-[2-(diethylamino)ethoxy]anilino]-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one as a white solid of melting point 123-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-0b471e50ed8b41918463788dcf930ed3
Source noteuspto-grants-2000_11