Sodium Hydroxide → HCID 131732142, Verbindung

HRID 1400078Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1400078
NO.Cl.[OH-].[Na+].CC1[N:8]([C@H:13]2[CH2:20][C@@:19]3([C:21]([O:23][CH2:24][C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=4)=[O:22])[C@H:15]([CH2:16][CH2:17][CH2:18]3)[CH2:14]2)C(C)=CC=1>O.CO>[NH2:8][C@H:13]1[CH2:20][C@@:19]2([C:21]([O:23][CH2:24][C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)=[O:22])[C@H:15]([CH2:16][CH2:17][CH2:18]2)[CH2:14]1

Komponenten

6

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

To a aqueous solution of NH2OH.HCl (8.4 g, 121.2 mmol) and NaOH (2.2 g, 19.54 mmol) in H2O (20 mL) was added a solution of Example 48C (2.81 g, 8.36 mmol) in MeOH (70 mL) and the mixture was heated at 65° C. for 8 hours. The mixture was cooled to room temperature, sufficient water was added and MeOH was removed under reduced pressure. The resulting slurry was adjusted to pH=10 with NaOH solution (2.5 N) and extracted with dichloromethane. The combined organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated to give a crude product, which was purified by column chromatography (SiO2, dichloromethane:MeOH from 100:1 to 10:1) to get the title compound.

Aufarbeitung

  1. temperatureThe mixture was cooled to room temperature
  2. customMeOH was removed under reduced pressure
  3. extractionextracted with dichloromethane
  4. washThe combined organic layer was washed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give a crude product, which
  9. customwas purified by column chromatography (SiO2, dichloromethane:MeOH from 100:1 to 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-08a65a1261474907988c5d5c461e5fb4
Quelldatensatz
uspto-grants-2014_12
Patentnummer
US08906911B2

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