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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858249Generated: October 30, 2026

4-(2-(Diethylamino)ethoxy)aniline → HCID 21988163, compound

https://huagongshe.com/reaction/1858249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(Diethylamino)ethoxy)anilineHCID 418932—
Reactant3-(2-bromophenyl)-7-methanesulfonyl-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 21988153—
SolventDichloromethane methanol acetic acid waterHCID 18914200—
ProductHCID 21988163HCID 219881638.4%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 200 mg (0.5 mmol) of 3-(2-bromophenyl)-7-methanesulfonyl-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one and 208 mg (1 mmol) of 4-[2-(diethylamino)ethoxy]aniline was heated at 180° C. for 30 minutes and then cooled. The residue was subjected to column chromatography on silica gel using dichloromethane/methanol/acetic acid/water (240:24:3:2) for the elution. Product-containing fractions were combined and evaporated and the residue was 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 give 22 mg (8%) of 3-(2-bromophenyl)-7-[4-[2-(diethylamino)ethoxy]anilino]-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one as a cream colored solid of melting point 144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-98e3e8f1f1a24cf68f2895e1cce77afb
Source noteuspto-grants-2000_11