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Acetic Acid → Methyl (5R)-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-L-prolinate

HRID 2264832
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2264832
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[CH2:17][CH2:18][C@@H:19]([C:21]([O:23][CH3:24])=[O:22])[N:20]=2)=[N:14][CH:15]=1.C(O)(=O)C.FC(F)(F)C(O)=O>C(OCC)(=O)C.[Pt]>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]([C@@H:16]2[NH:20][C@H:19]([C:21]([O:23][CH3:24])=[O:22])[CH2:18][CH2:17]2)=[N:14][CH:15]=1
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Komponenten

6

Edukt 3

HCID 176Acetic AcidHCID 6422Trifluoroacetic acidHCID 59596699Methyl (2S)-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-3,4-dihydro-2H-pyrrole-2-carboxylate

Produkt 1

HCID 59596692Methyl (5R)-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-L-prolinateAusbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23939
Platinum
Katalysator
HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

To a solution of methyl (2S)-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-3,4-dihydro-2H-pyrrole-2-carboxylate (D85, 300 mg, 0.91 mmol) in ethyl acetate was added platinum on activated carbon (70 mg, 5 wt. % dry basis Degussa type F101 RAW) and the mixture was stirred under hydrogen atmosphere (P=1 atm) for 4 hours. After a further addiction of acetic acid (0.4 ml) and stirring for 12 hours the reaction wasn't complete. A further addiction of catalyst (70 mg) and trifluoroacetic acid was required before the reaction was complete. The catalyst was filtered off, the solvent removed under reduced pressure and the residue filtered on scx cartridge. The residue was purified by chromatography on silica gel using cyclohexane/ethyl acetate (7:3 to 6:4) to afford the title compound as a colourless oil (180 mg, 60%). Rt (HPLC): 3.69 min; MS: (ES/+) m/z: 331 [MH]+ C18H19FN2O3 requires 330; 1H NMR (400 MHz, CDCl3) δ (ppm): 8.27-8.43 (m, 1H); 7.45-7.56 (m, 1H); 7.38-7.44 (m, 1H); 7.31-7.38 (m, 1H); 7.24-7.31 (m, 1H); 7.15-7.23 (m, 1H); 7.08-7.15 (m, 1H); 5.18 (s, 2H); 4.32-4.41 (m, 1H); 3.98-4.05 (m, 1H); 3.79 (s, 3H); 2.19-2.31 (m, 2H); 2.04-2.13 (m, 1H); 1.77-1.90 (m, 1H).

Aufarbeitung

  1. filtrationThe catalyst was filtered off
  2. customthe solvent removed under reduced pressure
  3. filtrationthe residue filtered on scx cartridge
  4. customThe residue was purified by chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-9c0a893f68924d1fb9574b2392269750
Quelldatensatz
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07855218B2

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