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HRID 1352944作成日:2026年10月27日

p-Toluenesulfonic acid monohydrate → 2-Benzo[1,3]dioxol-5-yl-1-(4-methanesulfonyl-phenyl)-4-trifluoromethyl-1H-imidazole

https://huagongshe.com/reaction/1352944

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物5-[1-[4-(methylsulfonyl)phenyl]-4-hydroxy-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl)-1,3-benzodioxoleHCID 10598616—
溶媒TolueneHCID 1140—
生成物2-Benzo[1,3]dioxol-5-yl-1-(4-methanesulfonyl-phenyl)-4-trifluoromethyl-1H-imidazoleHCID 1078769880%

反応手順

A mixture of 5-[1-[4-(methylsulfonyl)phenyl]-4-hydroxy-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]-1,3-benzodioxole from Step 2 (1.26 g, 2.9 mmol) and p-toluenesulfonic acid monohydrate (200 mg) in toluene (50 mL) was heated to reflux for 72 hours. The reaction mixture was cooled and the solvent removed under reduced pressure. The crude residue was redissolved in methylene chloride and washed with water, aqueous sodium bicarbonate and brine. After drying (Na2SO4), filtration and concentration in vacuo, the crude mixture (1.34 g) was purified by chromatography on silica gel using toluene/ethyl acetate 1/1 to give pure 5-(1-(4-(methylsulfonyl)phenyl)-4-(trifluoromethyl)-1H-imidazol-2-yl]-1,3-benzodioxole (940 mg, 80%) as a white solid: mp (DSC) 165° C. Anal Calc'd. for C18H13N2SO4F3: C, 52.68; H, 3.19; No 6.83. Found: C, 53.05; H, 3.19; N, 6.65.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07220770B2
出典データセットuspto-grants-2007_05
ORD IDord-b95842a6bb264da6b999789e4e395504
出典メモuspto-grants-2007_05