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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7751생성일: 2026년 10월 23일

1,2-Dimethoxyethane → 2-[3-Methoxy-4-(pyridin-3-ylmethyl)phenyl]-1,3-benzoxazole

https://huagongshe.com/ko/reaction/7751

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참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Potassium CarbonateHCID 11430—
반응물3-Pyridinylboronic acidHCID 2734378—
반응물2-[4-(Bromomethyl)-3-methoxyphenyl]-1,3-benzoxazoleHCID 21990991—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물2-[3-Methoxy-4-(pyridin-3-ylmethyl)phenyl]-1,3-benzoxazoleHCID 10236648—

반응 조건

온도80 °C

반응 단계

A mixture of 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole (190 mg, 0.58 mmol), 3-pyridylboronic acid (70 mg, 0.58 mmol), Pd(Ph3P)4 (70 mg, 0.06 mmol), K2CO3 (200 mg, 1.5 mmol), DME (6 mL) and H2O (3 mL) was degassed with bubbling Ar for 15 min. The mixture was heated at 80° C. for 1 h. The reaction was poured into H2O (40 mL) and extracted with CH2Cl2 (2×30 mL). The organic extracts were dried (MgSO4) and concentrated to afford a colorless solid. Purification of the solid by flash chromatography on silica gel (EtOAc:hexanes 3:1) afforded the desired 2-[3-methoxy-4-(pyridin-3-ylmethyl)phenyl]-1,3-benzoxazole as a yellow solid: 1H NMR (CDCl3, 300 MHz) δ 8.56 (br s, 1H), 8.45 (br d, 1H), 7.74–7.80 (m, 3H), 7.50–7.58 (m, 2H), 7.32–7.37 (m, 2H), 7.17–7.24 (m, 2H), 4.00 (s, 2H), 3.93 (s, 3H). MS (ESI) 317 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-a07ed9330a9844e9a2231169eeda2c61
출처 메모uspto-grants-2006_08