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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73244Generated: October 29, 2026

Methanesulfonyl chloride → HCID 178441166, compound

https://huagongshe.com/reaction/73244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59703946HCID 59703946—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178441166HCID 17844116679.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 172 mg (0.52 mmol) of N-(5-tert-butyl-isoxazol-3-yl)-2-methyl-2-(pyrrolidin-3-ylmethylsulfanyl)-propionamide (prepared according to Method I, step 1) and 0.18 mL (1.04 mmol) of N,N-diisopropylethylamine in THF were added 0.16 mL (2.11 mmol) of methanesulfonyl chloride. The reaction was heated within a microwave to 90° C. for 0.5 h. The mixture was concentrated under reduced pressure. The residue was dissolved in DCM (5 mL) and washed with saturated aqueous NaHCO3 solution (5 mL). The organic layer was dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure to afford 168 mg of N-(5-tert-butyl-isoxazol-3-yl)-2-(1-methanesulfonyl-pyrrolidin-3-ylmethylsulfanyl)-2-methyl-propionamide, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829034B2
Source datasetuspto-grants-2014_09
ORD IDord-2a2529c63b77412a91e1cd95f8ee4bd0
Source noteuspto-grants-2014_09