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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535875Generated: October 30, 2026

Sodium hydride → HCID 58459912, compound

https://huagongshe.com/reaction/535875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-1-piperidine-1-yl-ethanoneHCID 222312—
ReactantHCID 67036583HCID 67036583—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58459912HCID 58459912—

Reaction Steps

To a solution of 3-methyl-7,8,9,9a,10,11-hexahydro-5H-pyrido[3′,2′:4,5]pyrrolo[3,2-f]indolizine (100 mg, 0.440 mmol) in DMF (1 mL) was added a suspension of sodium hydride (52 mg, 1.32 mmol) in DMF (1 mL). After stirring for 5 min at RT, a solution of 2-chloro-1-(piperidin-1-yl)ethanone (142 mg, 0.881 mmol) in DMF (1 mL) was added to the reaction mixture, and stirring continued for 2 h. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue obtained was purified by silica gel flash chromatography to yield 2-(3-methyl-8,9,9a,10-tetrahydro-5H-pyrido[3′,2′:4,5]pyrrolo[3,2-f]indolizin-11(7H)-yl)-1-(piperidin-1-yl)ethanone;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859561B2
Source datasetuspto-grants-2014_10
ORD IDord-88db7dc25de84f78982d10f9a0db17e7
Source noteuspto-grants-2014_10