戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1364441作成日:2026年10月25日

Triethylamine → 2-[1-(3-Iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile

https://huagongshe.com/reaction/1364441

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Iodobenzoyl chlorideHCID 74378—
反応物2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochlorideHCID 66924378—
生成物2-[1-(3-Iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrileHCID 6692444195%

反応手順

A mixture of 2-fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride (200 mg; 0.7 mmol) (Example 123, Step 3) was stirred at room temperature with 3-iodobenzoyl chloride (187 mg; 0.7 mmol) and triethylamine (0.3 mL; 2.1 mmol) for 16 hours. Reaction was cooled and quenched with dilute HCl and mixture extracted with ethyl acetate (2×20 mL). Combined organics washed with water, saturated sodium bicarbonate, brine and dried over Na2SO4. Crude solid was obtained as 2-[1-(3-iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile. (310 mg; 95% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07888366B2
出典データセットuspto-grants-2011_02
ORD IDord-1214fe052fb740e9b9578e18bc2f4443
出典メモuspto-grants-2011_02