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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071756Generated: November 1, 2026

N,N-Diethylethylenediamine → 1,2-Ethanediamine, N2-(2-chloro-4-quinazolinyl)-N1,N1-diethyl-, hydrochloride (1:2)

https://huagongshe.com/reaction/2071756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DiethylethylenediamineHCID 60993—
Reactant2,4-DichloroquinazolineHCID 252886—
SolventTetrahydrofuranHCID 8028—
Product1,2-Ethanediamine, N2-(2-chloro-4-quinazolinyl)-N1,N1-diethyl-, hydrochloride (1:2)HCID 21412343169.1%

Reaction Steps

To a solution of 43.2 g of 2-diethylaminoethylamine (N,N-diethylethylenediamine) in 400 ml of tetrahydrofuran was added 54 g of 2,4-dichloroquinazoline. The mixture was stirred at ambient temperature overnight. The reaction mixture was evaporated almost to dryness and the residue was suspended in water. The aqueous medium was made alkaline with dilute sodium hydroxide and was extracted several times with ether. The combined ether extracts were washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was saturated with anhydrous hydrogen chloride. The solid which precipitated was isolated by filtration and then was recrystallized from ethanol and ether, giving 53.8 g of 2-chloro-4-(2-diethylaminoethylamino)quinazoline dihydrochloride which decomposed at 152°. The following analytical data were obtained:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04048312
Source datasetuspto-grants-1977_09
ORD IDord-b69b91fa6f2e44aa9b71307ca6f770a6
Source noteuspto-grants-1977_09