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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015626Generated: November 1, 2026

Benzo[b]furan-2-boronic acid → HCID 67299252, compound

https://huagongshe.com/reaction/1015626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo[b]furan-2-boronic acidHCID 2776266—
ReactantHCID 20775758HCID 20775758—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 67299252HCID 67299252100%

Reaction Steps

To a degassed solution of 3-[(4-Chloro-2,5-dimethyl-benzenesulfonyl)-(3-iodo-benzyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester (110 mg, 0.169 mmol) and benzofuran-2-boronic acid (55 mg, 0.185 mmol) in a mixture of DME (8 mL) and 2M aqueous Na2CO3 (4 mL), Pd(PPh3)4 (9 mg) was added and the reaction mixture was stirred at reflux conditions for 2 h under a N2 atmosphere. The reaction mixture was diluted with ethyl acetate and water. The organic layer was separated, dried (Na2SO4) and concentrated. 3-[(3-Benzofuran-2-yl-benzyl)-(4-chloro-2,5-dimethyl-benzenesulfonyl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester (107 mg, 100%) was isolated as a thick syrup and used for the next reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-b73d432eb94f433d9c0471c19d1b344e
Source noteuspto-grants-2011_07