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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7784생성일: 2026년 10월 23일

4-Chlorophenyl trifluoromethanesulphonate → 2-[4-(5-Chloropyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazole

https://huagongshe.com/ko/reaction/7784

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorophenyl trifluoromethanesulphonateHCID 581424—
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-[4-(5-Chloropyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazoleHCID 10308751—

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 (100 mg, 0.28 mmol) was reacted with 4-chlorophenyl trifluoromethanesulfonate (74 mg, 0.28 mmol) to afford the desired 2-[4-(5-chloropyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazole as a colorless solid: 1H NMR (CDCl3, 300 MHz) δ 8.69–8.68 (d, 1H), 7.98 (s, 2H), 7.94–7.90 (m, 2H), 7.86–7.78 (m, 1H), 7.74–7.73 (m, 1H), 7.65–7.58 (m, 1H), 7.40–7.37 (m, 2H), 4.03 (s, 3H). MS (ESI) 337 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-e4addf6843844e34bf17ccec7031bdb4
출처 메모uspto-grants-2006_08