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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397706Generated: October 29, 2026

Methanesulfonyl chloride → HCID 23001031, compound

https://huagongshe.com/reaction/397706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 23000985HCID 23000985—
SolventPyridineHCID 1049—
ProductAmmoniaHCID 222—
ProductHCID 23001031HCID 23001031130.3%

Reaction Steps

To a solution of 4-(3-aminophenyl)-N-hexylpiperidine (Preparation 50, 178 mg, 0.68 mmol) in pyridine (5 ml) at room temperature under an atmosphere of nitrogen was added methanesulfonyl chloride (79 ml, 1.03 mmol) over 10 min. The resultant mixture was stirred overnight, poured onto water (10 ml) and extracted with ethyl acetate (3×10 ml). The combined extracts were dried (MgSO4) and concentrated in vacuo at 80° C. to give the crude product which was purified by silica column chromatography, eluting with ethyl acetate:hexane:0.880 ammonia (90:9:1) to give the title compound as a pale brown oil (150 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610711B2
Source datasetuspto-grants-2003_08
ORD IDord-c74909ffbc4646608e0422ed6cbddb69
Source noteuspto-grants-2003_08