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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665069Generated: October 30, 2026

Sodium Carbonate → N-Benzyl-N-[5-[3-(methylsulfonyl)-4-(hydroxymethyl)phenyl]thiophene-2-ylmethyl]-2-(trifluoromethyl)benzenesulfonamide

https://huagongshe.com/reaction/1665069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantCesium fluorideHCID 25953—
Reactant(2-(Methylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanolHCID 59251458—
ReactantN-benzyl-N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamideHCID 67439229—
CatalystHCID 178418807HCID 178418807—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN-Benzyl-N-[5-[3-(methylsulfonyl)-4-(hydroxymethyl)phenyl]thiophene-2-ylmethyl]-2-(trifluoromethyl)benzenesulfonamideHCID 2521058339%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of N-benzyl-N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide (example 1, step 2, 170 mg), [2-methanesulfonyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanol (CAS [918328-16-2], 90 mg), cesium fluoride (88 mg) and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium dichloromethane adduct (12 mg) in a 1 M aqueous sodium carbonate solution (0.72 mL) and 1,2-dimethoxyethane (1.5 mL) was heated to 80° C. for 36 h. After cooling to r.t., the mixture was filtered. The filtrate was diluted with ethyl acetate and washed with water. The organic phase was dried (MgSO4), filtered and concentrated under reduced pressure. The product was purified by chromatography (SiO2, cyclohexane/ethyl acetate 1:0 to 0:1) to give N-benzyl-N-[5-(4-hydroxymethyl-3-methanesulfonyl-phenyl)-thiophen-2-ylmethyl]-2-trifluoromethyl-benzenesulfonamide (67 mg) as an off-white solid. MS: 612.6 ([M+NH4]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039493B2
Source datasetuspto-grants-2011_10
ORD IDord-0acb9b7649b54d45a106638a39c171ee
Source noteuspto-grants-2011_10