HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(2-Chloroacetyl)-1,2,3,4-tetrahydroquinolin-2-one → HCID 178512604, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(2-Chloroacetyl)-1,2,3,4-tetrahydroquinolin-2-one | HCID 4961790 | — |
| Reactant | HCID 178513045 | HCID 178513045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178512604 | HCID 178512604 | — |
Reaction Steps
A mixture of 6-(chloroacetyl)-3,4-dihydrocarbostyril (7 g), amidinothiourea (3.8 g) and absolute ethanol (250 ml) is stirred under reflux for about 24 hours. The reaction mixture is cooled to ice bath temperature and the precipitate filtered, washed with ethanol, and dried. The solid is suspended in aqueous sodium hydroxide, filtered, the filtered solid washed with water, and dried in vacuo. The dried solid is recrystallized from 50% aqueous DMF, and dried in vacuo yielding 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-36234ec5af314deeaa38db29bd0aa876 |
| Source note | uspto-grants-1988_01 |