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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048023Generated: November 1, 2026

Methanesulfonamide → HCID 58042386, compound

https://huagongshe.com/reaction/2048023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86660842HCID 86660842—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58042386HCID 5804238613.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of methanesulfonamide (93.4 mg, 0.98 mmol) in THF (2 mL) at room temperature was added potassium tert-butoxide (119 mg, 1.06 mmol) in one portion with stirring under nitrogen for 15 minutes. 4-Methylphenyl-5-chloro-4-[(5-chloro-6-isopropoxypyridin-3-yl)thio]-2-fluorobenzoate (Preparation 224, 352 mg, 0.75 mmol) was added as a solution in THF (2 mL). The mixture was then heated at 60° C. for 3 hours and then left at room temperature for 18 hours. The solvent was concentrated in vacuo and the residue was partitioned between EtOAc (10 mL) and water (5 mL). The organic layer was separated and then washed with 1M NaOH (5 mL), 2M HCl (5 mL), saturated aqueous brine (5 mL), dried over MgSO4 filtered and evaporated. The residue was triturated with acetone/heptane (1:9) to afford a white solid which was filtered and washed with heptane to yield the title compound (45 mg, 13%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592629B2
Source datasetuspto-grants-2013_11
ORD IDord-639a9398898f4b87ab0f1a054384d22e
Source noteuspto-grants-2013_11