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HRID 52304作成日:2026年10月24日

p-Chlorophenacyl bromide → 2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole

https://huagongshe.com/ja/reaction/52304

反応式

関与物質

役割名称HCID仕込み量
反応物p-Chlorophenacyl bromideHCID 68303—
反応物Sodium BicarbonateHCID 516892—
反応物4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
溶媒IsopropanolHCID 3776—
生成物2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazoleHCID 2214896955%

反応手順

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (700 mg, 2.24 mmol) and sodium bicarbonate (376 mg, 4.48 mmol) in isopropanol (30 mL), 4-chlorophenacyl bromide (1.05 g, 4.48 mmol) was added. After heating the reaction mixture at 80°-85° C. for 18 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was chromatographed (silica gel, hexane/ethyl acetate, 6/4) to give 2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole (545 mg, 55%) as a pale yellow solid: mp 169°-171° C. Anal. Calc'd. for C22H16N2SO2Cl12 : C, 59.60, H, 3.64, N, 6.32, S, 7.23. Found: C, 59.86, H, 3.80, N, 6.10, S, 7.27.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616601
出典データセットuspto-grants-1997_04
ORD IDord-ac86626c127242c192cab62d8b87aacd
出典メモuspto-grants-1997_04