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HRID 1767290作成日:2026年10月27日

Morpholine → Gabapentin Enacarbil

https://huagongshe.com/reaction/1767290

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物Allyl 1-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-1-Cyclohexane AcetateHCID 9999163—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒AcetonitrileHCID 6342—
生成物Gabapentin EnacarbilHCID 9883933—

反応手順

To a stirred solution of compound (15) (1 g, 2.7 mmol) in acetonitrile (10 mL) under nitrogen was added (10 mg, 0.008 mmol) of tetrakis(triphenylphosphine) palladium (0) followed by morpholine (0.28 mL, 0.28 g, 3.2 mmol). After one hour, the solvent was removed in vacuo. The resulting oil was dissolved in diethyl ether (50 mL) and the organic phase was washed with 2N HCl (20 mL), water (20 mL) and brine (20 mL). The ether layer was dried over anhydrous sodium sulfate and concentrated to give an oil, which was purified by column chromatography on silica gel, eluting with 30% ethyl acetate:hexane. The desired product (11) was isolated as a white crystalline solid (0.75 g, 84% yield), 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-67c2575901d44143b82ddf25c02faef2
出典メモuspto-grants-2007_06