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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473118Generated: November 1, 2026

Triethylamine → (R)-N-methyl-3-(2-(1-methylethylsulfonamido)-2,3-dihydro-1H-inden-5-yloxy)benzene sulfonamide

https://huagongshe.com/reaction/473118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-boronobenzenesulfonamideHCID 44886921—
Reactant(R)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamideHCID 68156499—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(R)-N-methyl-3-(2-(1-methylethylsulfonamido)-2,3-dihydro-1H-inden-5-yloxy)benzene sulfonamideHCID 68155814—

Reaction Steps

To a mixture of the 3-(N-methylsulfamoyl)phenylboronic acid (0.274 mmol, 59 mg), copper (II)acetate (0.137 mmol, 25 mg), triethylamine (0.685 mmol, 96 μL) and 4 Å molecular sieves (100 mg) in DCM (1 mL) was added (R)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide (0.137 mmol, 35 mg) and the resultant mixture stirred at room temperature overnight. The reaction mixture was diluted with DCM (1 mL) before water (0.5 mL) was added and the organic layers separated using hydrophobic frits. The aqueous was extracted with further DCM (1 mL), and the combined organics concentrated using to dryness. The residue was taken up in DMSO and purified by preparative HPLC to give the title compound as a clear film (5.9 mg, 10.1%). MS (ESI): m/z [M−H]− 423.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633237B2
Source datasetuspto-grants-2014_01
ORD IDord-e2f61ae4af4c4e0f8b3bd5aec2e45fb5
Source noteuspto-grants-2014_01