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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643465Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → tert-Butyl 3-(2-(4-(2-(pyrrolidin-1-yl)ethyl)piperidin-1-ylsulfonyl)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1643465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-[2-(Pyrrolidin-1-yl)ethyl]piperidineHCID 296293—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59367796HCID 59367796—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 3-(2-(4-(2-(pyrrolidin-1-yl)ethyl)piperidin-1-ylsulfonyl)ethyl)piperidine-1-carboxylateHCID 59367815—

Reaction Steps

tert-Butyl 3-(2-(perfluorophenoxysulfonyl)ethyl)piperidine-1-carboxylate (0.5 g, 1.09 mmol) and 4-(2-pyrrolidinoethyl)piperidine (0.4 g, 2.18 mmol) were dissolved in tetrahydrofuran (10 ml), 1,8-diazabicyclo[5.4.0]undec-7-ene (0.5 ml, 3.27 mmol) was added under an inert gas and the mixture was refluxed for 2 h. Ethyl acetate and saturated sodium bicarbonate solution (20 ml of each) were added, the phases were separated and the aqueous phase was extracted with ethyl acetate (2×30 ml). The combined organic phases were washed with saturated sodium chloride solution (20 ml), dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica gel) with ethyl acetate/methanol/ammonia (25% aq) (300:100:1). Yield: 0.32 g (64%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119805B2
Source datasetuspto-grants-2012_02
ORD IDord-779647ec967e4caaade07e048c0f48a4
Source noteuspto-grants-2012_02