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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7783생성일: 2026년 10월 23일

2-Bromo-6-methoxypyridine → 2-[3-Methoxy-4-(6-methoxypyridin-2-yl)phenyl]-1,3-benzoxazole

https://huagongshe.com/ko/reaction/7783

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참여 물질

역할이름HCID투입량
반응물2-Bromo-6-methoxypyridineHCID 256810—
반응물2-[4-(6-Bromopyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazoleHCID 10309389—
반응물2-[3-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3-benzoxazoleHCID 21990986—
생성물2-[3-Methoxy-4-(6-methoxypyridin-2-yl)phenyl]-1,3-benzoxazoleHCID 10286618—

반응 단계

Utilizing the general procedure outlined in the synthesis of 2-[4-(6-bromopyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazole, 2-[3-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3-benzoxazole (200 mg, 0.57 mmol) was reacted with 2-bromo-6-methoxypyridine (65 μL, 0.57 mmol) to afford the desired 2-[3-methoxy-4-(6-methoxypyridin-2-yl)phenyl]-1,3-benzoxazole as a colorless solid: 1H NMR (CDCl3, 300 MHz) δ 7.96–7.95 (m, 2H), 7.89 (s, 1H), 7.82–7.79 (m, 1H), 7.67–7.60 (m, 3H), 7.39–7.36 (m, 2H), 7.14–7.12 (m, 1H), 4.00 (s, 3H), 2.65 (s, 3H). MS (ESI) 333 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-79f8843a1ec24cb78062ca26ed9f8d6e
출처 메모uspto-grants-2006_08