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HRID 458385作成日:2026年10月25日

2-Naphthalenesulfonyl chloride → 4-Hydroxy-1-(naphthalene-2-sulfonyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/458385

反応式

関与物質

役割名称HCID仕込み量
反応物2-Naphthalenesulfonyl chlorideHCID 7125—
反応物3-Piperidinecarboxylic acid, 4-oxo-, ethyl ester, hydrochloride (1:1)HCID 107315—
溶媒TetrahydrofuranHCID 8028—
溶媒HexamethyldisilazaneHCID 13838—
生成物4-Hydroxy-1-(naphthalene-2-sulfonyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl esterHCID 6943232897.9%

反応条件

温度140 °C

反応手順

A suspension of 31.15 g (150 mmol) 3-Ethoxycarbonyl-4-piperidone hydrochloride was suspended in 400 ml hexamethyldisilazane and heated under reflux (140° C.) for 2.5 h. The solution was evaporated complete, the residue dissolved in 400 ml THF and treated with 34 g (150 mmol) of naphthalene-2-sulfonylchloride in 150 ml THF. The reaction was stirred 16 h at room temperature, evaporated, treated with 400 ml aqueous 10% NaCl, stirred for 10 min and extracted with EtOAc (3×400 ml). The organic phase was dried (Na2SO4) and evaporated and crystallized from Et2O at 5° C. to give 53.1 g (90%) of 4-hydroxy-1-(naphthalene-2-sulfonyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester, MS: 362 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189756B2
出典データセットuspto-grants-2007_03
ORD IDord-5b798cdf8ee94f53ae60e11e60566366
出典メモuspto-grants-2007_03