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HRID 1644927作成日:2026年10月27日

Triphenyl phosphite → (S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylate

https://huagongshe.com/reaction/1644927

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)piperidin-1-yl)-5-nitronicotinateHCID 58324510—
反応物HCID 178418361HCID 178418361—
触媒PlatinumHCID 23939—
触媒Ammonium metavanadate [UN2859] [Poison]HCID 62684—
溶媒DichloromethaneHCID 6344—
生成物(S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylateHCID 5832449589%

反応手順

In a bomb hydroginator, (S)-methyl 6-(2-(methoxycarbonyl)piperidin-1-yl)-5-nitronicotinate (1.95 g, 6.03 mmol), triphenyl phosphite (0.019 ml, 0.060 mmol), ammonium vanadate (0.056 g, 0.483 mmol) and platinum (5% on carbon, 0.235 g, 0.060 mmol) were mixed in dichloromethane (Volume: 30.2 ml) to give a suspension. The bomb was sealed and pressurized to 110 psi with hydrogen gas. The reaction was stirred at 110 psi 16 h, depressurized, diluted with DCM (100 mL) and refluxed 10 minutes. The hot mixture was filtered through celite and washed with DCM (50 mL). The filtrate was concentrated in vacuo to yield 1.4 g (89%) of the product as a white solid and used without further purification. [M+H] calc'd for C13H15N3O3, 262. found, 262.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124606B2
出典データセットuspto-grants-2012_02
ORD IDord-ee24a82408f34591809e559ef685ca1a
出典メモuspto-grants-2012_02