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HRID 1767289作成日:2026年10月26日

Ammonium formate → Gabapentin Enacarbil

https://huagongshe.com/reaction/1767289

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物Allyl 1-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-1-Cyclohexane AcetateHCID 9999163—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Gabapentin EnacarbilHCID 9883933—

反応手順

To a stirred suspension of ammonium formate (3.4 g, 54 mmol) in ethanol (34 mL), was added compound (15) (10 g, 27 mmol) together with 10% Pd/C (1 g) under a nitrogen atmosphere. After one hour, the reaction mixture was filtered and the catalyst washed with ethanol (2×10 mL). The filtrates were combined and evaporated. The crude product was dissolved in diethyl ether (150 mL) and the organic phase was washed with 2N HCl (100 mL), water (100 mL) and brine (100 mL). The ether layer was dried over anhydrous sodium sulfate and concentrated to give a viscous liquid that crystallized upon standing. The product was recrystallized using 1:10 ethyl acetate:heptane (100 mL) to give the product (11) as a white, crystalline solid (7.9 g, 88%), m.p 63–64° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07232924B2
出典データセットuspto-grants-2007_06
ORD IDord-2f6a36ef9d804b6f8ca88b24d51148a4
出典メモuspto-grants-2007_06