Pyridine → Cetilistat

HRID 1169575Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1169575
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].ClC([O-])=O.Cl[C:17]([O:19][CH3:20])=O.N1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(OCC)(=O)C.CCCCC>[CH2:17]([O:19][C:20]1[O:5][C:4](=[O:6])[C:3]2[CH:7]=[C:8]([CH3:11])[CH:9]=[CH:10][C:2]=2[N:1]=1)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:4][CH2:3][CH2:2][CH2:10][CH3:9]

Komponenten

7

Edukt 4

HCID 1049PyridineHCID 6586Methyl chloroformateHCID 762552-Amino-5-methylbenzoic acidHCID 21226386Carbonochloridate

Produkt 1

HCID 9952916CetilistatAusbeute 31 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8003PentaneLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

2-Amino-5-methylbenzoic acid (2.71 g, 17.9 mmol, 0.87 eq.) was dissolved in pyridine (24 ml) and added to the chloroformate solution prepared above. The mixture was stirred at room temperature for 1.75 hours. Methyl chloroformate (13.6 ml, 176 mmol, 8.5 eq) was added slowly, then the mixture was left to stir at ambient temperature overnight. The mixture was diluted with ethyl acetate (20 ml) and washed with water (15 ml) and 10% aqueous citric acid (20 ml). The combined aqueous phases were extracted with ethyl acetate (20 ml). The organic extracts were combined and washed with water (20 ml) and brine (20 ml) then concentrated to give a solid. This was slurried in pentane (5 ml), filtered, then slurried in acetonitrile (5 ml), filtered and purified by flash chromatography on silica (1.5% diisopropylethylamine in dichloromethane) to give a white solid (2.51 g, 31%) δH (400 MHz, CDCl3) 0.87 (3H, t, J 6.8, CH2CH3), 1.24-1.45 (26H, m, 13×CH2), 1.75-1.83 (2H, m, OCH2CH2), 2.41 (3H, s, ArCH3), 4.41 (2H, t, J 6.7, OCH2), 7.30 (1H, d, J 8.3, ArH), 7.51 (1H, dd, J 8.5, 2.0, ArH), 7.90 (1H, d, J 1.1, ArH); m/z (ES+) 402 (MH+); MPt. 72-73° C.

Aufarbeitung

  1. customprepared above
  2. waitthe mixture was left
  3. stirringto stir at ambient temperature overnight
  4. washwashed with water (15 ml) and 10% aqueous citric acid (20 ml)
  5. extractionThe combined aqueous phases were extracted with ethyl acetate (20 ml)
  6. washwashed with water (20 ml) and brine (20 ml)
  7. concentrationthen concentrated
  8. customto give a solid
  9. filtrationfiltered
  10. filtrationfiltered
  11. custompurified by flash chromatography on silica (1.5% diisopropylethylamine in dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-aaabe8ca53394d9d8ae3c24c9a513dac
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07825113B2

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