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Ammonium Acetate → HCID 178513844, Verbindung

HRID 1463230
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1463230
[F:1][C:2]1[N:7]=[C:6]2[NH:8][N:9]=[C:10]([C:11]([O:13]C(C)(C)C)=O)[C:5]2=[CH:4][CH:3]=1.C([O-])(=O)C.[NH4+:22]>FC(F)(F)C(O)=O>[F:1][C:2]1[N:7]=[C:6]2[NH:8][N:9]=[C:10]([C:11]([NH2:22])=[O:13])[C:5]2=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 517165Ammonium AcetateHCID 178450870HCID 178450870, Verbindung

Produkt 1

HCID 178513844HCID 178513844, VerbindungAusbeute 89,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

t-Butyl 6-fluoro-1H-pyrazolo[3,4-b]pyridine-3-carboxylate (8.90 g, 37.5 mmole) was dissolved in 30 mL of trifluoroacetic acid and allowed to stand undisturbed for 2 hours. The solvent was then evaporated and the residue was dissolved in 30 mL of DMF. N,N'-Carbonyldiimidazole (7.0 g, 43.2 mmol) was added and the reaction mixture was stirred overnight. Ammonium acetate (8.7 g, 113 mmol) was then added to the resulting suspendion and stirring was continued for 4 hours. The solvent was evaporated under high vacuum and the residue was triturated well with H2O to give 6.02 g (89%) of product after drying. An analytical sample was obtained by recrystallization from HOAc, mp 295° C. (dec).

Aufarbeitung

  1. customThe solvent was then evaporated
  2. dissolutionthe residue was dissolved in 30 mL of DMF
  3. stirringstirring
  4. waitwas continued for 4 hours
  5. customThe solvent was evaporated under high vacuum
  6. customthe residue was triturated well with H2O

Quellen und Nachweise

ORD-Eintrag
ord-600a837bffa34c74a0c4966c53af5ea1
Quelldatensatz
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05300498

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