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HRID 1418425作成日:2026年10月25日

Trifluoromethanesulfonic anhydride → 1-(2-(Thien-2-yl) pyrid-5-ylmethyl)-5-(4-cyanobenzyl)imidazole

https://huagongshe.com/reaction/1418425

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物DiisopropylethylamineHCID 81531—
反応物(6-Thien-2-ylpyrid-3-yl)methanolHCID 15411145—
反応物1-Trityl-4-(4-cyanobenzyl)imidazoleHCID 15837533—
溶媒DichloromethaneHCID 6344—
生成物1-(2-(Thien-2-yl) pyrid-5-ylmethyl)-5-(4-cyanobenzyl)imidazoleHCID 9906709—

反応条件

温度-78 °C

反応手順

To a solution of 2-(thien-2-yl)-5-hydroxymethylpyridine (255 mg, 1.33 mmol) and diisopropylethylamine (0.464 mL, 2.66 mmol) in dichloromethane (7 mL) at -78° C. is added trifluoromethanesulfonic anhydride (0.224 mL, 1.33 mmol) and the mixture stirred at -78° C. for 1 hour. To this mixture is added a solution of 1-trityl-4-(4-cyanobenzyl)-imidazole (566 mg, 1.33 mmol) in dichloromethane (5 mL). The mixture is allowed to warm to ambient temperature and stirred for 2 hours. The solvent is evaporated in vacuo. The residue is dissolved in methanol (50 mL), heated at reflux for 1 hour, and the solvent is evaporated in vacuo. The residue is partitioned between dichloromethane and sat. aq. NaHCO3 solution. The organic layer is dried, (Na2SO4) and the solvent evaporated in vacuo. The residue is chromatographed to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05883105
出典データセットuspto-grants-1999_03
ORD IDord-bf3697adbfb64a4dbdec293f7204f8f8
出典メモuspto-grants-1999_03