戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2057294作成日:2026年10月27日

Imidazole → HCID 178463970、化合物

https://huagongshe.com/reaction/2057294

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 178464455HCID 178464455—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物HCID 178463970HCID 17846397010.2%

反応条件

温度50 °C

反応手順

400 mg (8.4 mmol) trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide were suspended in toluene and evaporated (3×), redissolved in 1 ml DMF and treated with 102.4 mg (1.5 mmol, 1.8 eq) imidazole. At 0° C., 176 mg (11.7 mmol, 1.4 eq) TBDMSCl in 2 ml DMF were added, and the reaction mixture was stirred at 50° C. for 1 h. The solution was added to an aqueous solution of NaHCO3 and extracted with ether. The organic layer was washed with water and brine, and dried over Na2SO4. 509 mg crude trans-N-[4-(5-{[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-ethyl-amino}-pentyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide were isolated as light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07335687B2
出典データセットuspto-grants-2008_02
ORD IDord-da79b530870943d2a64eeb5900391ac8
出典メモuspto-grants-2008_02