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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188264Generated: October 26, 2026

Trifluoroacetic acid → cyclopentyl-3-((3-(4-(methylsulfonamido)phenyl)-4-oxo-4H-chromen-7-yl)ethynyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/1188264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(Cyclopentyloxycarbonyloxy)succinimideHCID 15927743—
ReactantN-(4-(7-(azetidin-3-ylethynyl)-4-oxo-4H-chromen-3-yl)phenyl)methanesulfonamideHCID 71506445—
SolventDichloromethaneHCID 6344—
Productcyclopentyl-3-((3-(4-(methylsulfonamido)phenyl)-4-oxo-4H-chromen-7-yl)ethynyl)azetidine-1-carboxylateHCID 71506446—

Reaction Steps

To a mixture of N-(4-(7-(azetidin-3-ylethynyl)-4-oxo-4H-chromen-3-yl)phenyl)methanesulfonamide.trifluoroacetic acid salt (55 mgs, 0.140 mmol) in dichloromethane (3 mL) was added cyclopentyl 2,5-dioxopyrrolidin-1-yl carbonate (95 mgs, 0.42 mmol) and diisopropylethylamine (0.2 mL, 1.4 mmol), and the mixture was stirred at room temperature for 16 hours. The resulting mixture was concentrated under reduced pressure, and chromatographed (SiO2, 25% ethyl acetate/dichloromethane) to provide cyclopentyl-3-((3-(4-(methylsulfonamido)phenyl)-4-oxo-4H-chromen-7-yl)ethynyl)azetidine-1-carboxylate:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673966B2
Source datasetuspto-grants-2014_03
ORD IDord-227737d604f043dea950a514f9124930
Source noteuspto-grants-2014_03