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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1510288생성일: 2026년 10월 25일

Potassium Carbonate → 4-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

https://huagongshe.com/reaction/1510288

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물6-Fluoronicotinic AcidHCID 242819—
반응물2-Phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (4-piperidin-4-yl-phenyl)-amideHCID 52937157—
용매Dimethyl SulfoxideHCID 679—
생성물4-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acidHCID 4683380815.1%

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온도135 °C

반응 단계

A mixture of 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (4-piperidin-4-yl-phenyl)-amide (208 mg, 0.5 mmol) and 6-fluoronicotinic acid (72 mg, 0.5 mmol) in DMSO (2 L) containing potassium carbonate (135 mg, 1 mmol) was heated in a microwave at 135° C. for 35 minutes. The mixture was extracted with ethyl acetate and 0.1N hydrochloric acid. The organic layer was washed with water and brine. Solvents were evaporated and the residue was purified through ISCO column chromatography (silica gel, ethyl acetate in hexanes, 10% to 100% linear gradient). The collected fractions were concentrated and the white crystalline material was filtered to give 4-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-carboxylic acid (40.5 mg). LC-MS for C28H23F3N4O4 (m/e) calcd 536, obsd 537 (M+H). 1H-NMR is consistent with the desired structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08211914B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-b0af23d89d404c2b87ee4f40c3a1a8f9
출처 메모uspto-grants-2012_07