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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407219생성일: 2026년 10월 24일

Water → 2-Chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-3-(difluoromethoxy)pyridin-4-amine

https://huagongshe.com/ko/reaction/407219

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium fluorideHCID 25953—
반응물2-(4-Chloro-2-fluoro-3-methoxyphenyl)-1,3,2-dioxaborinaneHCID 57782419—
반응물6-Bromo-2-chloro-3-(difluoromethoxy)pyridin-4-amineHCID 86675404—
촉매HCID 178418476HCID 178418476—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-Chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-3-(difluoromethoxy)pyridin-4-amineHCID 8667540584.2%

반응 단계

6-Bromo-2-chloro-3-(difluoromethoxy)pyridin-4-amine (368 mg, 1.346 mmol), 2-(4-chloro-2-fluoro-3-methoxyphenyl)-1,3,2-dioxaborinane (395 mg, 1.615 mmol), PdCl2(PPh3)2 (47.2 mg, 0.067 mmol), and CsF (409 mg, 2.69 mmol) were combined in DME (2 mL) and H2O (2 mL) and heated in a Biotage microwave reactor at 110° C. for 15 min. The cooled reaction mixture was partitioned between EtOAc and H2O. The organic phase was dried, concentrated onto silica gel, and purified by flash chromatography (SiO2, EtOAc/hexane gradient). This process yielded the title compound as a white solid (0.4 g, 84%): mp 152-154° C.; 1H NMR (300 MHz, DMSO-d6) δ 7.63-7.50 (m, 1H), 7.42 (dd, J=8.7, 1.6, 1H), 7.16 (d, J=1.8, 1H), 7.02 (t, J=73.4, 1H), 6.70 (s, 2H), 3.93 (d, J=0.8, 3H); ESIMS m/z 354 ([M+H]+), 352 ([M−H]−).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754229B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-67c9ae402d9048d795b7fd9de05e6325
출처 메모uspto-grants-2014_06