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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986461Generated: November 2, 2026

Potassium Carbonate → HCID 68829901, compound

https://huagongshe.com/reaction/1986461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChlorothiazoleHCID 76429—
ReactantPotassium AcetateHCID 517044—
ReactantBoronHCID 5462311—
ReactantHCID 86605639HCID 86605639—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178418807HCID 178418807—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 68829901HCID 6882990175.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl [4-(4-methylphenyl)-2-neopentyl-6-trifluoromethanesulfonyloxy-quinolin-3-yl]methylcarbamate (3.97 g, 7.0 mmol), boron bispinacolate (3.55 g, 14.0 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium-dichloromethane (1:1) complex (0.15 g, 0.21 mmol), potassium acetate (2.06 g, 21 mmol) and dimethyl sulfoxide (50 ml) was stirred under an argon atmosphere at 100° C. for 2 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and a mixture of the residue, 2-chlorothiazole (2.68 g, 14.0 mmol), tetrakis(triphenylphosphine)palladium (0.80 g, 0.7 mmol), potassium carbonate (2.90 g, 21 mmol), ethanol (5 ml), toluene (30 ml) and water (5 ml) was stirred under an argon atmosphere at 100° C. for 10 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give ethyl 2-[3-[[(tert-butoxycarbonyl)amino]methyl]-4-(4-methylphenyl)-2-neopentyl-6-quinolinyl]-1,3-thiazole-4-carboxylate (3.02 g, yield 75%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547710B2
Source datasetuspto-grants-2009_06
ORD IDord-af786bb1b65c41e0ab1664708c76dd09
Source noteuspto-grants-2009_06