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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390102Generated: October 25, 2026

Methanesulfonyl chloride → N-(3-(6-chloro-4-iodopyridin-2-ylamino)cyclohexyl)methanesulfonamide

https://huagongshe.com/reaction/390102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN1-(6-chloro-4-iodopyridin-2-yl)cyclohexane-1,3-diamineHCID 86649873—
SolventPyridineHCID 1049—
ProductN-(3-(6-chloro-4-iodopyridin-2-ylamino)cyclohexyl)methanesulfonamideHCID 87178324—

Reaction Steps

To a solution of EXAMPLE 11A (100 mg, 0.3 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (50 mg, 0.4 mmol). The mixture was stirred at ambient temperature for 5 h and partitioned between ethyl acetate and brine. The organic phase was washed with brine and concentrated. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate to provide the title compound. Yield: 100 mg (82%). MS (DCI/NH3) m/z 430 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383624B2
Source datasetuspto-grants-2013_02
ORD IDord-9a914a045aa04c59866671a9903bff04
Source noteuspto-grants-2013_02