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Barbituric Acid → (2R,4S,4aS)-rel-11-fluoro-2,4,8-trimethyl-1,2,4,4a-tetrahydro-2'H,6H-spiro[isoxazolo[4,5-g][1,4]oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'H,3'H)-trione

HRID 578009
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 578009
[CH3:1][C@@H:2]1[CH2:7][N:6]([C:8]2[C:17]([CH:18]=O)=[CH:16][C:11]3[C:12]([CH3:15])=[N:13][O:14][C:10]=3[C:9]=2[F:20])[CH2:5][C@H:4]([CH3:21])[O:3]1.[NH:22]1[C:27](=[O:28])[CH2:26][C:25](=[O:29])[NH:24][C:23]1=[O:30]>C(O)(C)C.CO>[F:20][C:9]1[C:10]2[O:14][N:13]=[C:12]([CH3:15])[C:11]=2[CH:16]=[C:17]2[C:8]=1[N:6]1[CH2:5][C@@H:4]([CH3:21])[O:3][C@@H:2]([CH3:1])[C@@H:7]1[C:26]1([C:25](=[O:29])[NH:24][C:23](=[O:30])[NH:22][C:27]1=[O:28])[CH2:18]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 6211Barbituric AcidHCID 866580566-((2R,6S)-2,6-dimethylmorpholino)-7-fluoro-3-methylbenzo[d]isoxazole-5-carbaldehyde2×

Produkt 1

HCID 45381704(2R,4S,4aS)-rel-11-fluoro-2,4,8-trimethyl-1,2,4,4a-tetrahydro-2'H,6H-spiro[isoxazolo[4,5-g][1,4]oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'H,3'H)-trioneAusbeute 71 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887Methanol
Lösungsmittel
HCID 3776IsopropanolLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a stirred solution of 6-((2R,6S)-2,6-dimethylmorpholino)-7-fluoro-3-methylbenzo[d]isoxazole-5-carbaldehyde (Intermediate 34, 543 mg, 1.86 mmol) in isopropanol (50 ml) was added pyrimidine-2,4,6(1H,3H,5H)-trione (238 mg, 1.86 mmol), and the reaction mixture was stirred for 16 hours at 80° C. Solvent was removed and the residue was triturated with isopropanol. The solid was filtered, washed with isopropanol, and dried in vacuo. The filtrate was concentrated and purified on silica gel (30-50% EtOAc in hexanes). The product thus obtained was combined with the filtered solid in methanol and concentrated to give the title compound (528 mg, 71%) as a racemic mixture.

Aufarbeitung

  1. customSolvent was removed
  2. customthe residue was triturated with isopropanol
  3. filtrationThe solid was filtered
  4. washwashed with isopropanol
  5. customdried in vacuo
  6. concentrationThe filtrate was concentrated
  7. custompurified on silica gel (30-50% EtOAc in hexanes)
  8. customThe product thus obtained
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-76579a391f164837a42e15b302a5a9a1
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09040528B2

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