돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390782생성일: 2026년 10월 25일

Ethanol → 2-(Benzofuran-2-carbonylamino)-4-(4-methyl-3-nitro-phenyl)thiophene-3-carboxylic acid

https://huagongshe.com/reaction/390782

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물4-Methyl-3-nitrobenzeneboronic acidHCID 2773515—
반응물Tert-butyl 2-(benzofuran-2-carbonylamino)-4-(trifluoromethylsulfonyloxy)thiophene-3-carboxylateHCID 59225740—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물2-(Benzofuran-2-carbonylamino)-4-(4-methyl-3-nitro-phenyl)thiophene-3-carboxylic acidHCID 5953601481.7%

반응 단계

tert-butyl 2-(benzofuran-2-carbonylamino)-4-(trifluoromethylsulfonyloxy)thiophene-3-carboxylate (82, 50 mg, 0.102 mmol), 4-methyl-3-nitrophenylboronic acid (28 mg, 0.153 mmol), Tetrakis(triphenylphosphine)palladium(0) (1.0 mg, 0.001 mmol), and sodium carbonate (42 mg, 0.407 mmol), 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 84 as a white powder (35.2 mg, 43%). 1H NMR (500 MHz, DMSO d6) δ=13.48 (br, 1 H), 12.57 (br, 1 H), 7.96 (s, 1 H), 7.86 (m, 2 H), 7.76 (d, 1 H), 7.64 (d, 1 H), 7.57 (t, 1 H), 7.49 (d, 1 H), 7.42 (t, 1 H), 2.55 (s, 3 H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383670B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-6156b26d4eae44c9b33fb49456e4944e
출처 메모uspto-grants-2013_02