Acetic Anhydride → HCID 136199666, Verbindung

HRID 1699548Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1699548
[C:1]1([C:7]2[N:8]=[C:9]([C:12]3[CH:13]=[N+:14]([O-])[CH:15]=[CH:16][CH:17]=3)[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(OC(=O)C)(=[O:21])C>>[O:21]=[C:13]1[C:12]([C:9]2[S:10][CH:11]=[C:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[N:8]=2)=[CH:17][CH:16]=[CH:15][NH:14]1

Komponenten

3

Edukt 2

HCID 7918Acetic AnhydrideHCID 187071743-(4-phenylthiazol-2-yl)pyridine-N-oxide

Produkt 1

HCID 136199666HCID 136199666, Verbindung

Versuchsvorschrift

In 25 ml of acetic anhydride was dissolved 2.8 g of 3-(4-phenylthiazol-2-yl)pyridine-N-oxide. The solution was refluxed for 6 hours with heating. The solvent was removed by distillation. The residue was treated with ammonia water and extracted with dichloromethane. The extract was water-washed, dried and subjected to solvent removal by distillation. The residue was mixed with a small amount of dichloromethane. The resulting crystals were collected by filtration and recrystallized from methanol to obtain 60 mg of 2-(2-oxopyridin-3-yl)4-phenylthiazole as light brown plate crystals.

Aufarbeitung

  1. temperatureThe solution was refluxed for 6 hours
  2. temperaturewith heating
  3. customThe solvent was removed by distillation
  4. additionThe residue was treated with ammonia water
  5. extractionextracted with dichloromethane
  6. washwashed
  7. customdried
  8. customsubjected to solvent removal by distillation
  9. additionThe residue was mixed with a small amount of dichloromethane
  10. filtrationThe resulting crystals were collected by filtration
  11. customrecrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-34b38acc8eff4a76bb1aff35b51590e4
Quelldatensatz
uspto-grants-2002_02
Patentnummer
USRE037556E1

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