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Triethylamine → Methyl (R)-3-(N-Cyclobutyl-N-isopropylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxylate

HRID 1738322
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1738322
[CH:1]1([N:5]([C@@H:9]2[CH2:14][C:13]3[C:15](OS(C(F)(F)F)(=O)=O)=[CH:16][CH:17]=[C:18]([F:19])[C:12]=3[O:11][CH2:10]2)[CH:6]([CH3:8])[CH3:7])[CH2:4][CH2:3][CH2:2]1.[C]=O.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C.CN([CH:69]=[O:70])C.[CH3:71][OH:72]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:1]1([N:5]([C@@H:9]2[CH2:14][C:13]3=[C:15]([C:71]([O:70][CH3:69])=[O:72])[CH:16]=[CH:17][C:18]([F:19])=[C:12]3[O:11][CH2:10]2)[CH:6]([CH3:8])[CH3:7])[CH2:4][CH2:3][CH2:2]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 8471TriethylamineHCID 812191,3-Bis(diphenylphosphino)propaneHCID 21901440N,N-dimethylformamide methanolHCID 54082177(R)-3-(N-Cyclobutyl-N-isopropylamino)-8-fluoro-5-trifluoromethylsulfonyloxy-3,4-dihydro-2H-1-benzopyranHCID 178418416HCID 178418416, Verbindung

Produkt 1

HCID 53695439
Methyl (R)-3-(N-Cyclobutyl-N-isopropylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxylate
Ausbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 167845palladium(II) acetateKatalysator

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

(R)-3-(N-Cyclobutyl-N-isopropylamino)-8-fluoro-5-trifluoromethylsulfonyloxy-3,4-dihydro-2H-1-benzopyran (1.65 g, 4.01 mmol) was dissolved in a solution of DMF/methanol (6:2, 30 mL) and then degassed followed by the inlet of carbon monoxide (×3). With a slight positive pressure of carbon monoxide, palladium(II)-acetate (30 mg), 1,3-bis(diphenylphosphino)propane (55 mg) and triethylamine (1.25 mL, 8.8 mmol) were added and the reaction mixture was degassed and subjected to carbon monoxide once again. The reaction was heated to 70° C. under carbon monoxide atmosphere with vigorous stirring for 6 h. The reaction was allowed to cool and the solvent was removed in vacuo. The remains were taken into a 2M solution of NH3 and then extracted, twice, with diethyl ether. The combined ether portions were dried (MgSO4), filtered, and the solvent removed in vacuo to give the crude residue. Chromatography on silica (eluent: 8% ethyl acetate/hexane) gave 1.18 mg (92% yield) of the title compound as a clear oil. [α]21D =-139.1° (C=0.1; CHCl3). GC-MS (70 eV) M=321 (3%).

Aufarbeitung

  1. customdegassed
  2. customthe reaction mixture was degassed
  3. temperatureto cool
  4. customthe solvent was removed in vacuo
  5. extractionextracted
  6. dry with materialThe combined ether portions were dried (MgSO4)
  7. filtrationfiltered
  8. customthe solvent removed in vacuo
  9. customto give the crude residue

Quellen und Nachweise

ORD-Eintrag
ord-47739388784340e198437b62b867618a
Quelldatensatz
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05962514

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