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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1471583생성일: 2026년 10월 25일

Hydrochloric Acid → 5-Hydroxy-6-(1-hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-nicotinonitrile

https://huagongshe.com/reaction/1471583

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl EtherHCID 3283—
반응물6-(1-Hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-5-methoxymethoxy-nicotinonitrileHCID 67439660—
용매MethanolHCID 887—
생성물5-Hydroxy-6-(1-hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-nicotinonitrileHCID 6743987041.9%

반응 조건

온도65 °C

반응 단계

To a suspension of 6-(1-hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-5-yloxy)-5-methoxymethoxy-nicotinonitrile (0.28 g, 0.89 mmol) in methanol (4 mL) was added 1 M HCl in ether (1.79 mL, 1.79 mmol) at 0° C. The reaction was heated at 65° C. for 2 hours. Methanol was removed under reduced pressure and the product was purified by reverse phase prep HPLC using CH3CN/H2O (0.1% AcOH) as the eluent to yield the title compound (0.10 g, 41%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 9.22 (s, 1 H), 8.02 (s, 1 H), 7.76 (d, J=7.8 Hz, 1 H), 7.57 (s, 1 H), 7.19 (s, 1 H), 7.15-7.09 (m, 1 H), 4.98 (s, 2 H); MS (ES) m/z: 267 (M−1)−; HPLC purity 92.91% (Maxplot), 92.41% (220 nm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012431B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-5e816acf4b4041ce9aa99b4fa52c9eca
출처 메모uspto-grants-2015_04