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HRID 333859作成日:2026年10月26日

Pyridine → 5-{2-[2-Chloro-4-(4-fluoro-3-methoxy-phenoxy)-phenyl]-1-hydroxy-1-trifluoromethyl-propyl}-1-methyl-1H-pyridin-2-one

https://huagongshe.com/reaction/333859

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物(4-Fluoro-3-methoxyphenyl)boronic acidHCID 44558185—
反応物5-[2-(2-Chloro-4-hydroxy-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-1-methyl-1H-pyridin-2-oneHCID 57421314—
触媒Cupric acetateHCID 8895—
溶媒DichloromethaneHCID 6344—
生成物5-{2-[2-Chloro-4-(4-fluoro-3-methoxy-phenoxy)-phenyl]-1-hydroxy-1-trifluoromethyl-propyl}-1-methyl-1H-pyridin-2-oneHCID 5742131651.7%

反応手順

To a solution of 5-[2-(2-chloro-4-hydroxy-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-1-methyl-1H-pyridin-2-one (Example 196, 200 mg) in CH2Cl2 (4 ml) were added 4-fluoro-3-methoxyphenylboronic acid (282 mg), copper-(II)-acetate (307 mg), molecular sieve and pyridine (219 mg). The mixture was stirred at room temperature under an air atmosphere with exclusion of moisture for 7 days. The mixture was filtered, diluted with CH2Cl2 and washed with 1M aqueous HCl. The organic phase was dried (MgSO4), filtered and concentrated to dryness. The product was purified by chromatography (SiO2, cyclohexane/EtOAc 1:0=>0:1) to give the title compound (139 mg) as an off-white solid. MS (m/e)=486.3 [M+H+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883786B2
出典データセットuspto-grants-2014_11
ORD IDord-1022c9cfb3b3434f9a2212bd4e65af53
出典メモuspto-grants-2014_11