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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7768생성일: 2026년 10월 24일

Hydrochloric Acid → 7-Fluoro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazole hydrochloride

https://huagongshe.com/ko/reaction/7768

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Amino-6-fluorophenolHCID 643562—
반응물Trimethyl(phosphooxy)silaneHCID 16133246—
반응물3-Methoxy-4-(pyridin-2-yl)benzoic acidHCID 21956515—
용매Diethyl EtherHCID 3283—
생성물7-Fluoro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazole hydrochlorideHCID 10309038—

반응 조건

온도200 °C

반응 단계

To 7 mL trimethylsilyl polyphosphate was added 2-amino-6-fluorophenol (166 mg, 1.31 mmol) and 3-methoxy-4-pyridin-2-ylbenzoic acid (300 mg, 1.31 mmol). The mixture was heated at 200° C. for 2 h, quenched over ice, and made basic (pH 14) with 1N NaOH. The aqueous phase was extracted with EtOAc (3×150 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The resultant oil was taken up in ether and reconcentrated to give a tan solid. The free base was dissolved in ether and HCl (1N in ether) was added. The solution was filtered to give 7-fluoro-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazole hydrochloride as a yellow solid. 1H NMR (DMSO-d6, 300 MHz) δ 8.71 (d, 1H), 8.00 (t, 1H), 7.97–7.84 (m, 4H), 7.70 (d, 1H), 7.49–7.37 (m, 3H), 4.00 (s, 3H); MS (ESI) 321 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-9836977a6c9943028d1255113ebbcc1a
출처 메모uspto-grants-2006_08