HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Terazosin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| 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 | 108.1% |
Reaction Steps
To a solution of iso-propanol (290 ml), water (50 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 35 hours. Then the reaction mixture was cooled to room temperature and stirred at this temperature for about 12 hours. The crystals were collected by filtration, washed with iso-propanol and dried in vacuo at 40° C. to yield 38.8 g (94%) of Terazosin.HCl dihydrate. See Trial K in Table I. Trial L was performed using a 5% percent volume of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248888B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-b884f596763d41c59533e061ee197f02 |
| Source note | uspto-grants-2001_06 |