Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595573Generated: October 30, 2026

Cesium carbonate → HCID 90332468, compound

https://huagongshe.com/reaction/595573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-(3,6-Dihydro-2H-thiopyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 46739735—
Reactant5-bromo-2-iodo-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamideHCID 90332469—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 90332468HCID 9033246834%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-2-iodo-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide (800 mg, 1.6 mmol), 2-(3,6-dihydro-2H-thiopyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (371 mg, 1.6 mmol) and Cs2CO3 (1.07 g, 3.28 mmol) in 1,4-dioxane (20 mL) was added Pd(dppf)Cl2 (50 mg) and tri-o-tolylphosphine (50 mg) under nitrogen. The reaction mixture was heated at 100° C. for 4 h, concentrated in vacuo to remove 1,4-dioxane and purified by column chromatography (PE:EA=3:1) to give the compound 5-bromo-2-(3,6-dihydro-2H-thiopyran-4-yl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide (250 mg, yield: 33%). 1H-NMR (CDCl3, 400 MHz) δ 8.09 (s, 1H), 7.59 (s, 1H), 6.73 (s, 1H), 6.06 (brs, 1H), 3.38 (t, J=2.0 Hz, 2H), 3.30 (s, 3H), 3.05 (s, 3H), 3.00 (d, J=4.8 Hz, 3H), 2.87 (t, J=5.6 Hz, 2H), 2.70˜2.76 (m, 2H). MS (M+H)+: 459/461.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242998B2
Source datasetuspto-grants-2016_01
ORD IDord-a5ce715bfb334bf9908be98b3dadaca5
Source noteuspto-grants-2016_01