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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | 2,4-Dichloroquinazoline | HCID 252886 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Ethanediamine, N2-(2-chloro-4-quinazolinyl)-N1,N1-diethyl-, hydrochloride (1:2) | HCID 21412343 | 169.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04048312 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-b69b91fa6f2e44aa9b71307ca6f770a6 |
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| Source note | uspto-grants-1977_09 |
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