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HRID 379609作成日:2026年10月26日

Thionyl Chloride → Benzamide

https://huagongshe.com/reaction/379609

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物2,5-Dimethylpiperazine, trans-HCID 220672—
反応物Tetraethylammonium fluoride hydrateHCID 16211652—
反応物4-((3-((Tert-butyldimethylsilyl)oxy)phenyl)(hydroxy)methyl)-N,N-diethylbenzamideHCID 22350014—
生成物BenzamideHCID 2331—

反応手順

4-(3-(tert-Butyldimethylsilyloxy)-α-hydroxybenzyl)-N,N-diethylbenzamide (Example 1, infra) was treated with thionyl chloride and trans-2,5-dimethylpiperazine as described in Example 5. The crude mixture of diastereomers was purified by chromatography on silica gel (Waters Prep 500) with dichloromethane:ethanol:triethylamine (100:0.25:0.1). The less mobile isomer (1.28 g, 2.5 mmol) was dissolved in acetonitrile and treated with tetraethylammonium fluoride hydrate (0.6 g, 4.0 mmol) as in Example 7 to give 0.46 g of (±)-N,N-diethyl-4-((αR*)-3-hydroxy-α-((2R*, 5S*)-2,5-dimethyl-1-piperazinyl)benzyl)benzamide as a white solid, mp 175-177° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300332B1
出典データセットuspto-grants-2001_10
ORD IDord-e00d84cdcfe6456ca6342548a2d6eb36
出典メモuspto-grants-2001_10