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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285600Generated: November 2, 2026

Triethylamine → HCID 70546033, compound

https://huagongshe.com/reaction/2285600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-chloro-6-methylquinazolineHCID 940217—
Reactant2-(2-Methoxyphenoxy)ethyl amineHCID 1713005—
SolventBenzeneHCID 241—
ProductHCID 70546033HCID 7054603329.1%

Reaction Steps

To a solution of 1.8 g (0.01 mol) of 4-chloro-6-methylquinazoline in 50 ml of benzene were added 1.0 g (0.01 mol) of triethylamine and 1.7 g (0.01 mol) of 2-(0-methoxyphenoxy)ethylamine, and the mixture was heated, with stirring, at 60°~70° C. for 5 hours. After completion of the reaction, the benzene was evaporated under reduced pressure and the residue was dissolved in chloroform, washed with water and dried over anhydrous sodium sulfate. The chloroform was evaporated under reduced pressure to leave crystals, which were recrystallized from ethanol, giving 0.9 g of 6-methyl-4-[2-(2-methoxyphenoxy)ethyl]-aminoquinazoline in the form of colorless plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04323680
Source datasetuspto-grants-1982_04
ORD IDord-cd22d6c421534211be24b3d6ceec7ffd
Source noteuspto-grants-1982_04