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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355175Generated: October 31, 2026

Water → Bisegliptin

https://huagongshe.com/reaction/2355175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylamineHCID 7912—
Reactant(2S,4S)-1-(2-bromoacetyl)-4-fluoropyrrolidine-2-carbonitrileHCID 21090395—
ReactantEthyl 4-aminobicyclo[2.2.2]octane-1-carboxylateHCID 23149693—
SolventAcetonitrileHCID 6342—
ProductBisegliptinHCID 1168889488.3%

Reaction Steps

Ethyl 4-aminobicyclo[2.2.2]octane-1-carboxylate (92.0 mg) was dissolved in acetonitrile (2 mL) and diisopropylamine (100 μL) was added to the solution. While the mixture was chilled in an ice bath, (2S,4S)-1-(2-bromoacetyl)-4-fluoropyrrolidine-2-carbonitrile (100 mg) in acetonitrile (1 mL) was added dropwise. The mixture was stirred for 1.5 hours while chilled in the ice bath. Subsequently, water was added and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluant: ethyl acetate:methanol=5:1) to give (2S,4S)-1-[[N-(4-ethoxycarbonylbicyclo[2.2.2]oct-1-yl)amino]acetyl]-4-fluoropyrrolidine-2-carbonitrile (132 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754757B2
Source datasetuspto-grants-2010_07
ORD IDord-e7428ce307ff4b2992dfe1f3db9d28ad
Source noteuspto-grants-2010_07