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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515122Generated: October 30, 2026

4-Cyanobenzenesulfonyl chloride → HCID 71565861, compound

https://huagongshe.com/reaction/515122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 90410636HCID 90410636—
SolventDimethylformamideHCID 6228—
ProductHCID 71565861HCID 71565861—

Reaction Steps

To a vial containing (R)-5-(2-(3-(aminomethyl)azetidin-1-yl)-1-hydroxyethyl)-4-methylisobenzofuran-1(3H)-one hydrochloride [INTERMEDIATE 12] (0.17 g, 0.54 mmol) was added commercially available 4-cyanobenzene-1-sulfonyl chloride (0.20 g, 1.0 mmol) as a solution in DMF (500 μL) followed by diisopropylethylamine (0.16 g, 1.2 mmol). The vial was shaken for 24 hours, and then was concentrated in vacuo. The resulting residue was dissolved in DMSO (1 mL) and purified by HPLC to provide (R)-4-cyano-N-((1-(2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethyl)azetidin-3-yl)methyl)benzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108947B2
Source datasetuspto-grants-2015_08
ORD IDord-924888d629c344dcadcf7f099a093cbb
Source noteuspto-grants-2015_08