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HRID 407219作成日:2026年10月26日

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

https://huagongshe.com/reaction/407219

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cesium fluorideHCID 25953—
反応物2-(4-Chloro-2-fluoro-3-methoxyphenyl)-1,3,2-dioxaborinaneHCID 57782419—
反応物6-Bromo-2-chloro-3-(difluoromethoxy)pyridin-4-amineHCID 86675404—
触媒HCID 178418476HCID 178418476—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-3-(difluoromethoxy)pyridin-4-amineHCID 8667540584.2%

反応手順

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]−).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754229B2
出典データセットuspto-grants-2014_06
ORD IDord-67c9ae402d9048d795b7fd9de05e6325
出典メモuspto-grants-2014_06