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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1020821생성일: 2026년 10월 23일

Water → 5-Cyclopropyl-6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(4-oxopentyloxy)nicotinonitrile

https://huagongshe.com/ko/reaction/1020821

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-olHCID 57968699—
반응물6-Chloro-5-cyclopropyl-2-(4-oxopentyloxy)nicotinonitrileHCID 86661729—
용매Dimethyl SulfoxideHCID 679—
생성물5-Cyclopropyl-6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(4-oxopentyloxy)nicotinonitrileHCID 66726180—

반응 조건

온도40 °C

반응 단계

A mixture of 6-chloro-5-cyclopropyl-2-(4-oxopentyloxy)nicotinonitrile (360 mg, 1.29 mmol), compound benzo[c][1,2]oxaborole-1,5(3H)-diol (232 mg, 1.55 mmol) and Cs2CO3 (505 mg, 1.55 mmol) in DMSO (20 mL) was stirred at 40° C. overnight. The mixture was diluted by water, extracted by EtOAc, the separated organic layer was concentrated in vacuo and the residue was purified by column chromatography (Petroleum ether:EtOAc=10:1˜3:1) to afford 5-cyclopropyl-6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-(4-oxopentyloxy)nicotinonitrile. (200 mg, 40%). 1H-NMR (400 MHz, DMSO-d6) δ (ppm) 9.20 (s, 1H), 7.86 (s, 1H), 7.75 (d, J=8.0, 1H), 7.24 (d, J=2.0, 1H), 7.16 (dd, J=8.0, 2.0, 1H), 4.97 (s, 2H), 3.94 (t, J=7.8, 2H), 3.29 (t, J=7.8, 2H), 2.02 (m, 4H), 1.65 (t, J=7.8, 2H), 0.92 (m, 2H), 0.77 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08716478B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-857a57b80c944aacbcb62f82c18ab102
출처 메모uspto-grants-2014_05