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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603524Generated: October 25, 2026

Tetrahydrofuran → 4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-Trimethoxyquinazoline

https://huagongshe.com/reaction/1603524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-6,7,8-trimethoxyquinazolineHCID 100686—
Reactant4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
SolventIsopropanolHCID 3776—
Product4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-TrimethoxyquinazolineHCID 979845072%

Reaction Steps

1.0 g of ethyl 4-aminobutyrate hydrochloride (6.0 mmol), 2 ml of triethylamine, 10 ml of tetrahydrofuran and 10 ml of 2-propanol are added to 0.50 g (2.0 mmol) of 4-chloro-6,7,8-trimethoxyquinazoline, followed by heating under reflux one whole day and night. The reaction liquid is distilled under reduced pressure to remove the solvent. The obtained residue is purified by silica gel column chromatography (ethyl acetate) and then recrystallized from ethyl acetate/hexane. Thus, 0.49 g (yield 72%) of a white crystal is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990117
Source datasetuspto-grants-1999_11
ORD IDord-f89c6bd37f1e46618a85f45d67f39c63
Source noteuspto-grants-1999_11