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HRID 2077866Erstellt: 26. Oktober 2026

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/2077866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenyl phosphiteHCID 7540—
Edukt(S)-methyl 6-(2-(methoxycarbonyl)piperidin-1-yl)-5-nitronicotinateHCID 58324510—
EduktHCID 178418361HCID 178418361—
KatalysatorPlatinumHCID 23939—
KatalysatorAmmonium metavanadate [UN2859] [Poison]HCID 62684—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylateHCID 5832449589%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07928105B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-89d0ab0bf7f042f18ad8dde0f1c0a40e
Quellennotizuspto-grants-2011_04