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HRID 983058作成日:2026年10月25日

Oxalyl chloride → 1-Piperidinepropanoyl chloride

https://huagongshe.com/reaction/983058

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物1-Piperidinepropanoic acidHCID 117782—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1-Piperidinepropanoyl chlorideHCID 22561913—

反応手順

To a solution of 3-piperidin-1-yl-propionic acid (472 mg, 3 mmol) in DCM (15 mL) at 0° C. was added oxalyl chloride (4.5 mmol) followed by one drop of DMF. After stirring for 2 hours at rt, the solvent was removed to give 3-piperidin-1-yl-propionyl chloride as a white solid. To a solution of 1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepine (347 mg, 2.55 mmol) in DCM (10 mL) was added TEA (1 eq.) and 1-piperidinepropionic acid chloride. The mixture was stirred at rt for overnight. The reaction was diluted with DCM, washed with NaHCO3, brine, dried and concentrated. The residue was purified on a silica gel column to give 230 mg of 3-piperidin-1-yl-1-(5,6,7,8-tetrahydro-1H-pyrrolo[3,2-b]azepin-4-yl)-propan-1-one as a light brown gel.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06861418B2
出典データセットuspto-grants-2005_03
ORD IDord-57cc1dd9d8cc4eceb216ee373141d977
出典メモuspto-grants-2005_03