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HRID 2077823作成日:2026年10月25日

Triphenyl phosphite → (S)-methyl6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazine-3-carboxylate

https://huagongshe.com/reaction/2077823

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenyl phosphiteHCID 7540—
反応物(S)-Methyl 6-(2-(methoxycarbonyl)pyrrolidin-1-yl)-5-nitronicotinateHCID 58324504—
触媒PlatinumHCID 23939—
触媒Ammonium metavanadateHCID 516859—
溶媒DichloromethaneHCID 6344—
生成物(S)-methyl6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazine-3-carboxylateHCID 5832444980%

反応手順

(S)-Methyl 6-(2-(methoxycarbonyl)pyrrolidin-1-yl)-5-nitronicotinate (1.45 g, 46.9 mmol) and triphenyl phosphite (5.00 mg, 0.0161 mmol) were dissolved in dichloromethane (12 mL). Ammonium metavanadate (50 mg, 0.427 mmol) and Pt/C (5% wt., 200 mg) were added and the reaction mixture was stirred under hydrogen (80 psi) for 5 h. The reaction mixture was filtered through a small plug of celite and the precipitate was washed multiple times with hot dichloromethane until it was free from white precipitate. The filtrate was concentrated in vacuo and crystallized with ethyl ether (15 mL). The resulting solid was filtered off and dried in vacuum to afford the title compound as an off-white solid (0.930 g, 80%). [M+H] calc'd for C12H13N3O3, 248; found, 248.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07928105B2
出典データセットuspto-grants-2011_04
ORD IDord-074bf43c9a2542dbbbce01c07b292215
出典メモuspto-grants-2011_04