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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24658Generated: October 26, 2026

Potassium Carbonate → HCID 57297799, compound

https://huagongshe.com/reaction/24658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2,6-Dicyanophenyl)boronic acidHCID 22571817—
ReactantHCID 22970630HCID 22970630—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
ProductHCID 57297799HCID 5729779965.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2,6-dicyanobenzene boronic acid (0.516 g) and anhydrous K2CO3 (0.52 g) in DME/H2O (10 mL/0.5 mL) under N2 was added N-(2,6-dichlorobenzoyl)-O-(trifluoromethanesulfonyl)-L-tyrosine methyl ester (0.5 g), The catalyst Pd(PPh3)4 (0.1 g) was added and the mixture was heated at 80° C. for 5 h. The mixture was cooled, diluted with EtOAc and washed successively with water and brine. The organic layer was dried (MgSO4), evaporated, and the residue was purified by column chromatography (silica gel; eluent: EtOAc/hexane 3/1)) to yield 325 mg of N-(2,6-dichlorobenzoyl)-4-(2-cyano-6-carbamoyl-phenyl)-L-phenylalanine methyl ester. ESMS: m/z 496 (MH+), 494 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855843B2
Source datasetuspto-grants-2005_02
ORD IDord-63da51aaf48841ae8aa3c85e908b845a
Source noteuspto-grants-2005_02