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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541205Generated: November 1, 2026

(Bis(2-methoxyethyl)amino)sulfur trifluoride → HCID 68288303, compound

https://huagongshe.com/reaction/541205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
ReactantHCID 68288835HCID 68288835—
SolventDichloromethaneHCID 6344—
ProductHCID 68288303HCID 6828830339.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of tert-butyl 4-(5-cyanopyridin-2-yl)-4-hydroxypiperidine-1-carboxylate (compound 26.2, 1 g, 3.13 mmol, 1.00 equiv, 95%) in dichloromethane (50 mL) under nitrogen at −78° C. was added dropwise a solution of bis(2-methoxyethyl)aminosulfur trifluoride (830 mg, 3.75 mmol, 1.20 equiv) in dichloromethane (10 mL) during the course of 1 min. The resulting mixture was stirred for 1 h at −78° C. The reaction was then carefully quenched by dropwise addition of water and washed with 2×20 mL of sodium bicarbonate(aq) followed by 3×20 mL of brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:10) to yield 0.38 g (38%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-3a69f528d7c340fc80fc0219e72f09c7
Source noteuspto-grants-2014_10