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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602521Generated: October 29, 2026

Potassium Carbonate → HCID 67267387, compound

https://huagongshe.com/reaction/602521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantQuinoline-3-boronic acidHCID 2734663—
ReactantHCID 67267453HCID 67267453—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetoneHCID 180—
ProductHCID 67267387HCID 6726738733.2%

Reaction Conditions

Temperature125 °C

Reaction Steps

{4-[(5-Chloro-thiophen-2-ylmethyl)-amino]-2-iodophenyl}-carbamic acid ethyl ester (15 mg), 3-quinolineboronic acid (29.7 mg), palladium(II) acetate (ca. 1 mg), potassium carbonate (0.035 mL, 5M aqueous solution), and acetone (2 mL) were mixed and heated in heated in a sealed glass tube in a microwave synthesizer for 10 minutes at 125° C. After cooling to room temperature, the reaction mixture was extracted with ethyl acetate (4 mL), the organic phase washed with water (2×2 mL), and brine (2×2 mL), dried over magnesium sulfate, and filtered. The solvent was removed in vacuo, and the crude product was purified by preparative LC-MS. The collected fraction was evaporated in: vacuo, redissolved in ethyl acetate (5 mL), and the organic phase was washed with saturated aqueous sodium bicarbonate (3 mL), water (3 mL), and brine (2×2 mL). The organic phase was dried over magnesium sulfate, filtered, and the solvent was removed in vacuo to furnish the title compound (5 mg, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906537B2
Source datasetuspto-grants-2011_03
ORD IDord-bda9e553c766473b8c3c8f4acaddc944
Source noteuspto-grants-2011_03