HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Terazosin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| Reactant | 1-(Tetrahydro-2-furoyl)piperazine | HCID 2734641 | — |
| Solvent | Water | HCID 962 | — |
| Product | Terazosin | HCID 5401 | 101.5% |
Reaction Steps
To a solution of absolute ethanol (272 ml), water (68 ml) and N-(2-tetrahydrofuroyl)piperazine (20 g) were added, while stirring, 4-amino-2-chloro-6,7-dimethoxyquinazoline (22.2 g). The reaction mixture was heated to reflux and the reflux was maintained for about 32 hours. Then the reaction mixture was cooled to room temperature and stirred at this temperature for about 48 hours. The crystals were collected by filtration, washed with absolute ethanol and dried in vacuo at 40° C. to yield 36.44 g (85.5%) of Terazosin.HCl dihydrate. See Trial M in Table I. Trial N was performed using a 10% volume of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248888B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-6974a168f6cd404a8e52a190cb51185e |
| Source note | uspto-grants-2001_06 |