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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433202Generated: October 31, 2026

Sodium Carbonate → HCID 178527415, compound

https://huagongshe.com/reaction/1433202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-(Benzenesulfonyl)-2-bromoethanolHCID 53443523—
Reactant5-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-(4-trifluoromethyl-phenoxymethyl)-benzoimidazole-1-carboxylic acid tert-butyl esterHCID 57934968—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178527415HCID 17852741559.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2-(4-trifluoromethyl-phenoxymethyl)-benzoimidazole-1-carboxylic acid tert-butyl ester (0.046 g, 0.0887 mmol), 2-bromophenylsulfonylethanol (0.036 g, 0.133 mmol), sodium carbonate (0.056 g, 0.532 mmol), and 1,1′-[bis(di-tert-butylphosphino)ferrocene]-palladium dichloride (0.006 g, 0.00887 mmol) in DME (2 mL) and H2O (0.5 mL) was heated at 80° C. for 12 hours. The reaction mixture was concentrated under reduced pressure, and the residue was purified by chromatography (silica, EtOAc) to afford the title compound as a light brown solid (0.025 g, 59%). 1H NMR (400 MHz, CD3OD) δ (ppm): 8.17 (dd, 1H, J=8.0 Hz, J=1.2 Hz), 7.76-7.61 (m, 6H), 7.46 (dd, 1H, J=7.6 Hz, J=1.2 Hz), 7.34 (d, 1H, J=7.6 Hz), 7.26 (d, 2H, J=8.8 Hz), 5.46 (s, 2H), 3.63 (t, 2H, J=6.6 Hz), 2.91 (t, 2H, J=12.8 Hz). Mass Spectrum (LCMS, ESI pos.) Calcd. For C25H23F3N3O4S: 518.5 (M+MeCN+H), Found 518.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612211B2
Source datasetuspto-grants-2009_11
ORD IDord-86947884781444c7b30baa29cafc4579
Source noteuspto-grants-2009_11