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HRID 30518作成日:2026年10月26日

Ammonium formate → Gabapentin Enacarbil

https://huagongshe.com/reaction/30518

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US07423169B2
出典データセットuspto-grants-2008_09
ORD IDord-191ae72a0ffa4cf7a192af7f165a1881
出典メモuspto-grants-2008_09