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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573283Generated: October 29, 2026

N-bromobutanimide → 10-Bromo-6,7,8,9-tetrahydropyrido[2,3-b]indolizine

https://huagongshe.com/reaction/573283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant6,7,8,9-Tetrahydropyrido[2,3-b]indolizineHCID 66727772—
SolventDimethylformamideHCID 6228—
Product10-Bromo-6,7,8,9-tetrahydropyrido[2,3-b]indolizineHCID 6672788387.5%

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029536B2
Source datasetuspto-grants-2015_05
ORD IDord-1f2857067d2342888e4afa93d4e455e3
Source noteuspto-grants-2015_05