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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45248Generated: October 26, 2026

Potassium Carbonate → methyl N-[(6-chloropyridin-3-yl)sulfonyl]-N-cyclopentylglycinate

https://huagongshe.com/reaction/45248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
Reactant6-chloro-N-cyclopentylpyridine-3-sulfonamideHCID 16227304—
SolventAcetonitrileHCID 6342—
Productmethyl N-[(6-chloropyridin-3-yl)sulfonyl]-N-cyclopentylglycinateHCID 8665974594%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2 g (7.67 mmol) of 6-chloro-N-cyclopentylpyridine-3-sulfonamide, 0.7 mL (7.67 mmol) of methyl bromoacetate and 1.2 g (8.4 mmol) of K2CO3 in 15 mL of CH3CN is heated for 12 hours at 80° C. After cooling to room temperature, the medium is filtered and the filtrate is concentrated. The residue is taken up in 100 mL of DCM, washed successively with 50 mL of saturated NaHCO3 solution and 50 mL of water, and the organic phase is then dried over Na2SO4, concentrated under reduced pressure and purified by chromatography on a column of silica gel, eluting with an 8/2 heptane/EtOAc mixture. 2.4 g of methyl N-[(6-chloropyridin-3-yl)sulfonyl]-N-cyclopentylglycinate are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541455B2
Source datasetuspto-grants-2013_09
ORD IDord-714d01a295904cbcb2891931551fc56b
Source noteuspto-grants-2013_09