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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471791Generated: October 30, 2026

Isopropyl chloroformate → 4-[5-(2-Fluoro-4-methanesulfonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid isopropyl ester

https://huagongshe.com/reaction/1471791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(2-Fluoro-4-methanesulfonyl-phenyl)-2-piperidin-4-yl-furo[2,3-c]pyridineHCID 86694575—
SolventTetrahydrofuranHCID 8028—
Product4-[5-(2-Fluoro-4-methanesulfonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid isopropyl esterHCID 71736723—

Reaction Steps

Isopropyl chloroformate (1 mol/L in toluene; 0.30 mL) is added to a solution of 5-(2-fluoro-4-methanesulfonyl-phenyl)-2-piperidin-4-yl-furo[2,3-c]pyridine (75 mg) and N,N-diisopropyl-ethylamine (0.10 mL) in tetrahydrofuran (1 mL) chilled in an ice bath. The solution is stirred at room temperature for 3 h. The solution is concentrated and the residue is taken up in water and dichloromethane. The resulting mixture is extracted with dichloromethane and the combined extracts are dried (Na2SO4). The solvent is evaporated and the residue is purified by HPLC on reversed phase (methanol/water) to give the title compound. Mass spectrum (ESI+): m/z=461 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012456B2
Source datasetuspto-grants-2015_04
ORD IDord-bf59f56b5e914ef9bcedf7c45f352e73
Source noteuspto-grants-2015_04