HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448959Generated: October 27, 2026
2-Chloro-6,7-dimethoxy-4-quinazolinamine → Doxazosin Monohydrochloride
https://huagongshe.com/reaction/1448959
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| Reactant | N-1,4-Benzodioxane-2-carbonyl piperazine | HCID 2735449 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Doxazosin Monohydrochloride | HCID 11591230 | 75.4% |
Reaction Steps
4-Amino-2-chloro-6,7-dimethoxyquinazoline (140 g.) and N-(1,4-benzodioxan-2-carbonyl)piperazine (150 g.) were stirred together under reflux in n-butanol (2 l.) for 31/2 hours. The mixture was then cooled to 80° C., the solid product collected, washed with cold n-butanol (2×250 ml.), and dried. The crude product was dissolved in hot (80° C.) dimethylformamide (530 ml.) and water (130 ml.), filtered, concentrated in vacuo to about 300 ml., then cooled and ether (1.8 l.) added. The solid so obtained was collected and washed with ether to give 4-amino-2-[4-(1,4-benzodioxan-2-carbonyl)piperazin-1-yl]-6,7-dimethoxyquinazoline hydrochloride (215 g.), m.p. 289°-290° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04188390 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-4f0648326c2246dc88d983f1058208de |
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| Source note | uspto-grants-1980_02 |
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