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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345434Generated: October 30, 2026

N-Methylsulfamoyl chloride → HCID 19992426, compound

https://huagongshe.com/reaction/345434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methylsulfamoyl chlorideHCID 11789235—
ReactantHCID 19992424HCID 19992424—
SolventPyridineHCID 1049—
ProductHCID 19992426HCID 1999242639.6%

Reaction Steps

Methylsulphamoyl chloride (0.39 g) was added dropwise to a stirred solution of 4-[(4-aminophenoxy)methyl]-1-[4-pyridyl]-piperidine (see Preparation 4) (0.57 g) in pyridine (15 ml) and the mixture was stirred at room temperature for 6 hours. An additional 0.39 g of methylsulphamoyl chloride was then added and the mixture was stirred for a further 18 hours and then evaporated. The residue was partitioned between sodium bicarbonate solution and ethyl acetate. The organic layer was separated and the aqueous layer was extracted several times with ethyl acetate. The combined organic layers were washed with water, dried (Na2SO4) and evaporated. The solid residue was crystallised from ethanol to give the title compound, (0.30 g), m.p. 170.5°-172.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057528
Source datasetuspto-grants-1991_10
ORD IDord-4dcc3d9b79ea4841b42825ae199dd4ca
Source noteuspto-grants-1991_10