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HRID 245359Erstellt: 24. Oktober 2026

Barbituric Acid → (2r,4s,4As)-8-acetyl-9,10-difluoro-2,4-dimethyl-1,2,4,4a-tetrahydro-2'h,6h-spiro[1,4-oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'h,3'h)-trione

https://huagongshe.com/de/reaction/245359

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBarbituric AcidHCID 6211—
Edukt5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehydeHCID 58847058—
LösungsmittelIsopropanolHCID 3776—
Produkt(2r,4s,4As)-8-acetyl-9,10-difluoro-2,4-dimethyl-1,2,4,4a-tetrahydro-2'h,6h-spiro[1,4-oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'h,3'h)-trioneHCID 58847042—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a solution of 5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde (Intermediate 11, 3.0 g, 9.17 mmol) in IPA was added barbituric acid (1.4 g, 11.00 mmol), and the mixture was heated at 85° C. for 12 hours. Solvents were evaporated and the residue was purified over neutral alumina using a gradient of methanol in CH2Cl2 to give the title compound as a racemic mixture in the form of an off-white solid. Yield: 3.0 g (75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658641B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-3a2ef7a8c82541e096659b691eb6fea3
Quellennotizuspto-grants-2014_02