Sodium Carbonate → 3-Isoquinolinecarboxylic acid, 4-hydroxy-1-methyl-7-phenoxy-, methyl ester

HRID 523974

Reaktionsgleichung

Reaktionsgleichung von HRID 523974
C(O[CH2:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:14]=2)[C:9]([OH:23])=[C:8]([C:24]([O:26][CH3:27])=[O:25])[N:7]=1)(=O)C.C([O-])([O-])=O.[Na+].[Na+]>[Pd].C(OCC)(=O)C>[OH:23][C:9]1[C:10]2[C:15](=[CH:14][C:13]([O:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:12][CH:11]=2)[C:6]([CH3:5])=[N:7][C:8]=1[C:24]([O:26][CH3:27])=[O:25]

Komponenten

5

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A reactor was charged with 3c (16.0 g), Pd/C (2.08 g), anhydrous Na2CO3 (2.56 g) and ethyl acetate (120 mL). The flask was vacuum-purged with nitrogen (3×) and vacuum-purged with hydrogen (3×). The flask was then pressurized with hydrogen and stirred at about 60° C. until completion of reaction. The flask was cooled to 20-25° C., the pressure released to ambient, the head space purged with nitrogen three times and mixture was filtered. The filtrate was concentrated. Methanol was added. The mixture was stirred and then cooled. Product precipitated and was filtered and dried in an oven (Yield: 90%, HPLC: 99.7%).

Aufarbeitung

  1. customThe flask was vacuum-purged with nitrogen (3×)
  2. customvacuum-purged with hydrogen (3×)
  3. temperatureThe flask was cooled to 20-25° C.
  4. customthe head space purged with nitrogen three times and mixture
  5. filtrationwas filtered
  6. concentrationThe filtrate was concentrated
  7. additionMethanol was added
  8. stirringThe mixture was stirred
  9. temperaturecooled
  10. customProduct precipitated
  11. filtrationwas filtered
  12. customdried in an oven (Yield: 90%, HPLC: 99.7%)

Quellen und Nachweise

ORD-Eintrag
ord-2c6110184759494b9fed36e122797728
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09340511B2

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