Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413792Generated: November 1, 2026

2-Methoxyethanol → Terazosin

https://huagongshe.com/reaction/1413792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
Reactant2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
Reactant1-(Tetrahydro-2-furoyl)piperazineHCID 2734641—
SolventTriethylamineHCID 8471—
ProductTerazosinHCID 540186.6%

Reaction Steps

Sixty grams (0.25 M) of 2-chloro-4-amino-6,7-dimethoxyquinazoline and 56.8 grams (0.308 M) of N-(2-tetrahydrofuroyl)piperazine were added to a stirred solution of 500 grams of Methyl Cellosolve® (ethylene glycol monomethyl ether) and 37.9 grams of triethylamine. The reaction mixture was heated to and maintained at a temperature of between 115° to 120° C. for 8 hours, and then allowed to cool to room temperature overnight. The Methyl Cellosolve® ether was removed by vacuum distillation, the residue was taken up in 1920 ml of 45° C. filtered water, and the temperature of the solution was readjusted to 45° C. The pH was then adjusted to pH 2.5 with concentrated hydrochloric acid and the solution was mixed for 1 hour. The solution was then filtered and the pH adjusted to pH 8.3 with filtered ammonia water (28%). After heating for 1 hour at 65° C., the solution was cooled to 15° C. and held at a temperature of between 15°-20° C. for 16 hours. The resulting crystalline product was filtered, washed with cold water (15° C.) and dried in vacuo at 65° C. to yield 84 grams of anhydrous base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251532
Source datasetuspto-grants-1981_02
ORD IDord-58f52f00d3ab4346b7fcb79cecf1678f
Source noteuspto-grants-1981_02