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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390807Generated: November 1, 2026

Methanesulfonyl chloride → HCID 67070003, compound

https://huagongshe.com/reaction/2390807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 67070050HCID 67070050—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 67070003HCID 6707000361%

Reaction Steps

step 5—To a solution of 54 (156 mg, 0.415 mmol) in pyridine (5 mL) at 0° C. was added methanesulfonyl chloride (0.050 mL, 0.643 mmol). The reaction was gradually warmed to RT and stirred for 1.5 h then diluted with EtOAc. The organic layer was washed sequentially with saturated aqueous CuSO4, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified by SiO2 chromatography eluting with an EtOAc/hexane gradient (10 to 50% EtOAc) to afford 115 mg (61%) of N-(4-{2-[5-tert-butyl-2-hydroxy-3-(2-methoxy-pyridin-3-yl)-phenyl]-ethyl}-phenyl)-methanesulfonamide (56) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273773B2
Source datasetuspto-grants-2012_09
ORD IDord-9df3cc3447a24d7fa81d3570e1c87a46
Source noteuspto-grants-2012_09