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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858308Generated: November 1, 2026

4-(2-(Diethylamino)ethoxy)aniline → HCID 53662365, compound

https://huagongshe.com/reaction/1858308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(Diethylamino)ethoxy)anilineHCID 418932—
ReactantHCID 54348550HCID 54348550—
ProductHCID 53662365HCID 5366236533.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 500 mg (0.7 mmol) of 1-[3-(tert-butyldiphenylsilyloxyethyl)phenyl]-3-(2,4-dichlorophenyl)-3,4-dihydro-7-methanesulfonyl-pyrimido[4,5-d]pyrimidin-2(1H)-one and 1 g (4.8 mmol) of 4-[2-(diethylamino)ethoxy]aniline was heated at 180° C. for 30 minutes. The mixture was cooled and the product purified by column chromatography on silica gel using dichloromethane/methanol/acetic acid/water (240:24:3:2) for the elution. Product-containing fractions were combined, evaporated and the residue evaporated with toluene. The residue was then dissolved in 40 ml of dichloromethane, washed with 40 ml of saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate, filtered and evaporated to afford 200 mg (33%) of 1-[3-(tert-butyldiphenylsilyloxyethyl)phenyl]-3-(2,4-dichlorophenyl)-7-[4-[2-(diethylamino)ethoxy]anilino]-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one as a yellow gum. [Mass spectrum (ESI) MH+ =859].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-ad84ed6edc2e44a39f8eb12444a22e57
Source noteuspto-grants-2000_11