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HRID 30314作成日:2026年10月26日

Dimethylformamide → N-benzyl-2-(morpholin-4-carbonyl)-morpholine hydrochloride

https://huagongshe.com/reaction/30314

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物MorpholineHCID 8083—
反応物Oxalyl chlorideHCID 65578—
反応物4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 2776352—
溶媒1,1-DichloroethaneHCID 6365—
生成物N-benzyl-2-(morpholin-4-carbonyl)-morpholine hydrochlorideHCID 68436268—

反応条件

温度62.5 °C

反応手順

A 250 mL reactor under N2 is successively loaded with 91 (5 g, 19.41 mmol), dichloroethane (50 mL), DMF (0.014 mL, 1% mol) and oxalyl chloride (1.86 mL, 21.35 mmol). The mixture is heated up to 60-65° C. for 2 h, before being cooled to 0° C. Then, morpholine (6.93 g, 79.60 mmol) in dichloroethane (20 mL) is added over 15 min keeping the temperature below 10° C. The heterogeneous solution is post-agitated for 1 h 30 min at room temperature and quenched with water (30 mL). The biphasic mixture is filtered on a Hyflo Super Cel® (10 g), then after separation, the organic layer is concentrated under reduce pressure. The mixture is taken up with isopropanol (80 mL) and 12N HClaq (1.61 mL, 19.41 mmol), stirred for 10 min and concentrated under reduce pressure. The mixture is taken up with isopropanol (13 mL), heated to reflux until a homogeneous solution is formed, then it is cooled to room temperature. The precipitate is filtered, rinsed with isopropanol (10 mL) and dried under vacuum at 40° C. overnight to obtain 92 as an off-white powder with 79% overall yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423037B2
出典データセットuspto-grants-2008_09
ORD IDord-427226a221e043c0b74882f62f2c6aba
出典メモuspto-grants-2008_09