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HRID 1963723作成日:2026年10月27日

Diisopropylethylamine → N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1963723

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-Methylpiperidine-4-carbonyl chlorideHCID 436503—
反応物2-Amino-4-chloropyridineHCID 581866—
溶媒DichloromethaneHCID 6344—
生成物N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamideHCID 69008397—

反応条件

温度0 °C

反応手順

A flask was flame dried and placed under a nitrogen atmosphere. 1-methylpiperidine-4-carbonyl chloride (1 eq) in anhydrous methylene chloride was added to the flask and brought to 0° C. To this was added the solution containing 4-chloropyridin-2-amine (1 eq), and diisopropylethylamine (5 eq) in anhydrous methylene chloride, which was stirred for 1 hour at 0° C. Reaction concentrated and partitioned between water and ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated to give the crude product. Purification on silica gel, 10% methanol in methylene chloride to yield N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide as a slightly yellow crystal solid. HPLC=2.39 min; MS: MH+=254.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415382B2
出典データセットuspto-grants-2013_04
ORD IDord-d29a842058d24a01b12bd799e6ec409a
出典メモuspto-grants-2013_04