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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387501Generated: October 30, 2026

Ethanol → 2-(Benzofuran-2-carbonylamino)-4-(8-methyl-5-quinolyl)thiophene-3-carboxylic acid

https://huagongshe.com/reaction/387501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant(8-Methylquinolin-5-yl)boronic acidHCID 4715077—
ReactantTert-butyl 2-(benzofuran-2-carbonylamino)-4-(trifluoromethylsulfonyloxy)thiophene-3-carboxylateHCID 59225740—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(Benzofuran-2-carbonylamino)-4-(8-methyl-5-quinolyl)thiophene-3-carboxylic acidHCID 4618665931%

Reaction Conditions

Temperature70 °C

Reaction Steps

Tert-butyl 2-(benzofuran-2-carbonylamino)-4-(trifluoromethylsulfonyloxy)thiophene-3-carboxylate (7), (8-methyl-5-quinolyl)boronic acid (48), Tetrakis(triphenylphosphine)palladium(0), and sodium carbonate, were combined in 2:1:1 ethanol, toluene and water the biphasic mixture was stirred vigorously in sealed vial at 70° C. After 2 hours, the mixture was filtered through Celite and the Celite rinsed with methylene chloride. The organic fraction of the filtrate was washed with water, dried with sodium sulfate, filtered, concentrated, triturated in methanol, centrifuged, decanted and the resulting solid was dried under vacuum and treated with a 1:1 mixture of methylene chloride and trifluoroacetic acid. After 4 hours the mixture was concentrated in vacuo, and the residue triturated in methylene chloride, centrifuged, decanted and dried under high vacuum to give 49A as a white powder (18.1 mg, 31%). 1H NMR (500 MHz, DMSO d6) δ=12.93 (br, 1H), 12.60 (s, 1H), 8.94 (m, 1H), 8.01 (d, 1H), 7.89 (s, 1H), 7.87 (d, 1H), 7.75 (d, 1H), 7.66 (d, 1H), 7.57 (t, 1H), 7.54 (dd, 1H), 7.44-7.41 (m, 3H), 7.11 (s, 1H), 2.76 (s, 3H) ppm. ESI MS [M+H] 429.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372991B2
Source datasetuspto-grants-2013_02
ORD IDord-c564ec5730ad43a3a7592234191e4dec
Source noteuspto-grants-2013_02