StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

HCID 67281758, Verbindung → HCID 67282524, Verbindung

HRID 1187502
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1187502
C([O:8][C:9]1[C:14](=[O:15])[C:13]([CH2:16][C:17]([F:20])([F:19])[F:18])=[CH:12][N:11]([CH3:21])[C:10]=1[CH3:22])C1C=CC=CC=1.[H][H]>CO.[Pd]>[OH:8][C:9]1[C:14](=[O:15])[C:13]([CH2:16][C:17]([F:20])([F:18])[F:19])=[CH:12][N:11]([CH3:21])[C:10]=1[CH3:22]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 67281758HCID 67281758, VerbindungHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 67282524HCID 67282524, VerbindungAusbeute 69 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 887MethanolLösungsmittel2×

Versuchsvorschrift

A clear solution of 3-benzyloxy-1,2-dimethyl-5-(2,2,2-trifluoro-ethyl)-1H-pyridin-4-one (1.1 g, 3.53 mmol) in methanol (32 mL) was debenzylated using Pd/C (10 wt. %, dry basis, on activated carbon, wet, Degussa type E101 NE/W, 0.17 g) as catalyst in a hydrogen atmosphere at a pressure of 50 psi for 30 min. The reaction mixture was diluted with methanol (30 mL), and sonicated for 10 min. A CELITE™ bed was prepared on a sintered glass, and washed with 6M HCl (100 mL), followed by water (7×50 mL) and then methanol (2×50 mL) under suction. The reaction mixture was filtered through the pre-treated CELITE™ bed. The volume of the filtrate was reduced to about 20 mL by evaporation under reduced pressure. HPLC analysis (HPLC Method 1, Example 24) of the filtrate indicated the presence of about 42% (peak percent area) of the starting material. Another 150 mg of Pd/C was added, and the mixture was subjected to the debenzylation reaction condition for a further 20 min, and worked up as described above. The catalyst was filtered off, and the filtrate was evaporated to dryness to afford 3-hydroxy-1,2-dimethyl-5-(2,2,2-trifluoro-ethyl)-1H-pyridin-4-one as a solid product (0.54 g, 69% yield, HPLC Method 1 (Example 24), RT=9.9 min, HPLC purity (peak percent area): 99.3% at λ=280 nm). 1H NMR (DMSO-d5) δ ppm: 7.70 (s, 1H), 3.65 (s, 3H), 3.39 (q, J=11.5 Hz, 2H), 2.26 (s, 3H). MS-ESI (m/z) 222.2 ([M+1]+, 100%), 202.2, 182.2.

Aufarbeitung

  1. customfor 30 min
  2. customsonicated for 10 min
  3. customA CELITE™ bed was prepared on a sintered glass
  4. washwashed with 6M HCl (100 mL)
  5. filtrationThe reaction mixture was filtered through the pre-treated CELITE™ bed
  6. customThe volume of the filtrate was reduced to about 20 mL by evaporation under reduced pressure
  7. additionAnother 150 mg of Pd/C was added
  8. customthe mixture was subjected to the debenzylation reaction condition for a further 20 min
  9. filtrationThe catalyst was filtered off
  10. customthe filtrate was evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-4fa4b9fda53b4d5f9284fcd16e136e78
Quelldatensatz
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08673943B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion