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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428378Generated: October 27, 2026

2-Chloro-6,7-dimethoxy-4-quinazolinamine → Doxazosin

https://huagongshe.com/reaction/428378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
ReactantN-1,4-Benzodioxane-2-carbonyl piperazineHCID 2735449—
Solvent1-ButanolHCID 263—
ProductDoxazosinHCID 315781%

Reaction Conditions

Temperature75 °C

Reaction Steps

4-amino-2-chloro-6,7-dimethoxyquinazoline (3.2 g, 13.35 mmol) and compound 1 (3.4 g, 13.75 mmol) prepared from Example 3 were dissolved in 72 mL of n-butanol. The mixture was refluxed under nitrogen for 3.5 hours. After cooling to 75° C., the solid product was obtained by filtration and dried to afford 5.25 g of hydrochloride salt of Doxazosin (10.76 mmol, 81% yield). 1 N NaOH solution was added to the salt. The mixture was heated to help the salt dissolved. After cooling, the mixture was extracted with 150 mL of dichloromethane twice. The organic layer was dried with anhydrous sodium sulfate and concentrated to afford 4.61 g of Doxazosin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313294B1
Source datasetuspto-grants-2001_11
ORD IDord-c0da6d462a2a4f0eb506784a32c61fdd
Source noteuspto-grants-2001_11