HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 6-(4-Acetoxypiperidino)-5-bromo-3,4-dihydrocarbostyril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-(4-Acetoxypiperidino)-3,4-dihydrocarbostyril | HCID 19094724 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-(4-Acetoxypiperidino)-5-bromo-3,4-dihydrocarbostyril | HCID 19094718 | — |
| Product | 6-(4-Acetoxypiperidino)-7-bromo-3,4-dihydrocarbostyril | HCID 19094725 | — |
Reaction Steps
To a solution of 300 mg of 6-(4-acetoxypiperidino)-3,4-dihydrocarbostyril in 7 ml of chloroform was added 370 mg of N-bromosuccinimide, and the mixture was stirred at room temperature for 1 hr. Then, an aqueous sodium thiosulfate was added to the reaction mixture, and the mixture was extracted with chloroform. The extract was washed with brine, dried and evaporated under a reduced pressure. The crude mixture was purified by a silica gel column chromatography to give 87 mg of 6-(4-acetoxypiperidino)-7-bromo-3,4-dihydrocarbostyril and 41 mg of 6-(4-acetoxypiperidino)-5-bromo-3,4-dihydrocarbostyril.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294718 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-6a4c00ab4b6745099a9539b782c4dfc4 |
| Source note | uspto-grants-1994_03 |