HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 10-Bromo-6,7,8,9-tetrahydropyrido[2,3-b]indolizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6,7,8,9-Tetrahydropyrido[2,3-b]indolizine | HCID 66727772 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 10-Bromo-6,7,8,9-tetrahydropyrido[2,3-b]indolizine | HCID 66727883 | 87.5% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 6,7,8,9-tetrahydropyrido[2,3-b]indolizine (170 mg) in DMF (3 mL) was added NBS (193 mg) at 0° C. The mixture was stirred at 0° C. for 30 min. The mixture was added saturated NaHCO3 aqueous solution at 0° C. and extracted with AcOEt. The organic layer was separated, washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (AcOEt/hexane) to give the title compound (217 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029536B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-1f2857067d2342888e4afa93d4e455e3 |
| Source note | uspto-grants-2015_05 |