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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 632226생성일: 2026년 10월 25일

Cesium carbonate → 5-Cyclopropyl-6-(tetrahydro-furan-2-ylmethoxy)-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/632226

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Potassium cyclopropyltrifluoroborateHCID 23697338—
반응물5-Bromo-6-(tetrahydro-furan-2-ylmethoxy)-pyridine-2-carboxylic acidHCID 71087728—
촉매palladium(II) acetateHCID 167845—
촉매Bis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물5-Cyclopropyl-6-(tetrahydro-furan-2-ylmethoxy)-pyridine-2-carboxylic acidHCID 7108725436%

반응 조건

온도120 °C

반응 단계

Palladium(II)acetate (1.19 mg, 5.3 μmol), butylbis(tricyclo[3.3.1.13,7]dec-1-yl)-phosphine (2.85 mg, 7.94 μmol, CAN 321921-71-5), potassium cyclopropyltrifluoroborate (39.6 mg, 267 μmol) and cesium carbonate (259 mg, 794 μmol) were combined to give a white solid. To this solid a degassed solution of 5-bromo-6-(tetrahydro-furan-2-ylmethoxy)-pyridine-2-carboxylic acid (80 mg, 265 μmol) in toluene (2.02 mL)/water (224 μL) was added through a septum cap. The reaction mixture was heated to 120° C. and stirred for 20 h. After cooling to ambient temperature the reaction mixture was diluted with water (2 mL), poured onto 20 mL ice water/brine/1 N HCl, extracted with isopropyl acetate (2×40 mL), and washed with 20 mL ice water/brine. The organic layers were dried with Na2SO4 and concentrated in vacuo to give a light brown oily residue which was purified by preparative TLC (silica gel, 2.0 mm, DCM/MeOH, 49:1). The title compound (25 mg, 36%) was isolated as light yellow liquid; MS (ESI): 262.0 [M−H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321727B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-615d170423664c159ec739c99c748ac9
출처 메모uspto-grants-2016_04