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HRID 1866643作成日:2026年10月26日

Acetic Acid → (+)-Ethyl [6-(3,5-difluorophenyl)-3,3-dimethyl-2-oxopiperazin-1-yl]acetate

https://huagongshe.com/reaction/1866643

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Glycine ethyl ester, hydrochlorideHCID 2723640—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Methyl 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]amino}-2-methylpropanoateHCID 66955347—
溶媒MethanolHCID 887—
生成物(+)-Ethyl [6-(3,5-difluorophenyl)-3,3-dimethyl-2-oxopiperazin-1-yl]acetateHCID 77577680—

反応手順

A mixture of methyl 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]amino}-2-methylpropanoate from Step A (8.60 g, 31.7 mmol), glycine ethyl ester hydrochloride (44.3 g, 317 mmol), and AcOH (5.71 mL, 95 mmol) in MeOH (300 mL) was stirred at ambient temperature for 10 min. NaCNBH3 (2.39 g, 38.0 mmol) was added and the pH of the mixture was checked and adjusted to pH ˜5 as necessary. The reaction mixture was heated to 50° C. for 18 h. Additional AcOH (4 mL) was added and the reaction mixture was heated to 60° C. for 6 h then allowed to cool and concentrated in vacuo to a volume of ca. 150 mL. The resulting mixture was carefully quenched with saturated aqueous NaHCO3 (300 mL) and then extracted with CH2Cl2 (1 L). The organic extract was washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with hexane:EtOAc—100:0 to 0:100, to give the title compound. MS: m/z=327 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07629338B2
出典データセットuspto-grants-2009_12
ORD IDord-2eca8ff6a6e64cd487df3214728fdc4c
出典メモuspto-grants-2009_12