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HRID 1364438作成日:2026年10月27日

3,4-Dichlorobenzyl chloride → 2-[1-(3,4-Dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile

https://huagongshe.com/reaction/1364438

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-Dichlorobenzyl chlorideHCID 7609—
反応物TriethylamineHCID 8471—
反応物2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochlorideHCID 66924378—
生成物2-[1-(3,4-Dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrileHCID 6692434373%

反応手順

A mixture of 2-fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride (240 mg; 0.89 mmol) (Example 126, Step 3) was heated with 3,4-dichlorobenzyl chloride (0.15 mL; 2.0 mmol) and triethylamine (0.3 mL; 2.0 mmol) to 50° C. 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 material was purified by chromatography using 0.5-2% methanol/DCM gradient to afford 2-[1-(3,4-dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile as a yellow oil. (280 mg; 73% 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-fd3d1fab9574435f909db733cffa76f3
出典メモuspto-grants-2011_02