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HRID 1166356作成日:2026年10月27日

3-Bromo-1,1,1-trifluoro-2-propanone → 2-[4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]pyridine

https://huagongshe.com/reaction/1166356

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 178504797HCID 178504797—
溶媒IsopropanolHCID 3776—
生成物2-[4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]pyridineHCID 2299798818%

反応条件

温度77.5 °C

反応手順

To a mixture of the amidine of step 1 (4.4 g, 16 mmol) and sodium bicarbonate (2.7 g, 32 mmol) in isopropanol (400 ml), 3-bromo-1,1,1-trifluoroacetone (2.5 ml, 24 mmol) was added. After heating at 75-80° C. for 24 hours, the reaction mixture was cooled and filtered. The residue was washed with methylene chloride and the combined organic fractions were dried over sodium sulfate, filtered and concentrated. The crude product (16.2 g) was purified by chromatography (silica gel, ethyl acetate/toluene 1/1) to give 2-[4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]pyridine (1.1 g, 18%) as a white solid: mp 195-198° C. Anal. Calc'd. for C16H14N3SO3F3: C, 49.87, H, 3.66, N, 10.90. Found: C, 50.13, H, 3.66, N, 10.30.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06613789B2
出典データセットuspto-grants-2003_09
ORD IDord-c8412f9c37364d1bb9972e301cd154c8
出典メモuspto-grants-2003_09