HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(2-Bromopropanoyl)-3,4-dihydroquinolin-2(1H)-one → HCID 178435112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(2-Bromopropanoyl)-3,4-dihydroquinolin-2(1H)-one | HCID 13051067 | — |
| Reactant | HCID 178513045 | HCID 178513045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178435112 | HCID 178435112 | — |
Reaction Steps
A mixture of 6-(α-bromopropionyl)-3,4-dihydrocarbostyril (7 g), amidinothiourea (3.1 g) and absolute ethanol (250 ml) is stirred under reflux overnight. The reaction mixture is cooled to ice bath temperature, and the solid filtered, washed with ethanol, dried, and suspended in aqueous sodium hydroxide. The neutralized solid is filtered, washed with water, dried and recrystallized from 50% aqueous DMF affording the desired product, M.P. >250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04721721 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-3d5c18740abd4ef8a1527eebc82cdcf1 |
| Source note | uspto-grants-1988_01 |