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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233414Generated: October 30, 2026

3-Cyanobenzene-1-sulfonyl chloride → HCID 59296073, compound

https://huagongshe.com/reaction/2233414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
Reactant(2R)-1-amino-3-[4-(3,4-dichlorophenoxy)piperidin-1-yl)propan-2-olHCID 11151315—
SolventPyridineHCID 1049—
ProductHCID 59296073HCID 5929607339.3%

Reaction Steps

To a solution of (2-R)-1-amino-3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]propan-2-ol (0.200 g, 0.63 mmol) in 4 ml of pyridine at 0° C. was added 3-cyanobenzenesulfonyl chloride (0.127 g, 0.63 mmol). After 30 min, the reaction was allowed to warm to room temperature and was stirred for 2 h. The reaction was concentrated under vacuum, and the residue partitioned between 10% aqueous sodium hydrogen carbonate and ethyl acetate. The organic layer was washed with water, then brine and dried over magnesium sulfate. The crude material was purified on silica gel (0 to 5% 7N ammonia in methanol/dichloromethane) to afford the title compound as a white foam (0.120 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709500B2
Source datasetuspto-grants-2010_05
ORD IDord-aa5352ad1a14476c89a3105b938b2146
Source noteuspto-grants-2010_05