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HRID 1450436作成日:2026年10月25日

Triethylamine → [Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanone

https://huagongshe.com/reaction/1450436

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物alpha-[1-(2-Phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanolHCID 18930341—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
生成物[Benzo[b]thiophene-2-yl][1-(2-phenylethyl)-4-piperidinyl]methanoneHCID 18930331—

反応条件

温度-78 °C

反応手順

Dissolve oxalyl chloride (4.22 g, 33.28 mmol) in methylene chloride (200 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, dimethylsulfoxide (5.42 g, 69.33 mmol) and stir at -78° C. for 15 minutes. Add, by dropwise addition, a solution of α-[1-(2-phenylethyl)-4-piperidinyl]-2-benzo[b]thiophenemethanol in dimethylsulfoxide (150 mL). Stir at -78° C. for 30 minutes, add triethylamine (15.18 g, 0.150 mol) and stir at -78° C. for 1 hour. Remove the ice bath and stir for an additional 1.5 hours. Evaporate the solvent in vacuo and recrystallize (isopropanol) to give the title compound as a fluffy white crystalline solid; mp 129°-130° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602147
出典データセットuspto-grants-1997_02
ORD IDord-ab9e7411503545679f9b56bfd49fdf54
出典メモuspto-grants-1997_02