1,3-Dichloro-5,5-dimethylhydantoin → Methyl 3-amino-2-chloroisonicotinate

HRID 2211004Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2211004
[NH2:1][C:2]1[CH:11]=[N:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[Cl:12]N1C(C)(C)C(=O)N(Cl)C1=O>ClC(Cl)=C(Cl)Cl>[NH2:1][C:2]1[C:11]([Cl:12])=[N:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]

Komponenten

4

Edukt 2

HCID 83601,3-Dichloro-5,5-dimethylhydantoinHCID 1488824Methyl 3-aminopyridine-4-carboxylate

Produkt 1

HCID 2762510Methyl 3-amino-2-chloroisonicotinate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 31373TetrachloroethyleneLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of 18 g (118 mmol) of methyl 3-aminoisonicotinate and 12 g (60 mmol) of 1,3-dichloro-5,5-dimethylhydantoin in 1500 mL of tetrachloroethylene was warmed slowly to 80° C. with stirring and held there for 3 hours. The solution was then cooled, filtered, washed with dilute aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain a dark oil. This oil was purified by careful column chromatography to give 6.7 g (30 percent of theory) of the title compound as a colorless solid melting at 91°-92° C.

Aufarbeitung

  1. temperatureThe solution was then cooled
  2. filtrationfiltered
  3. washwashed with dilute aqueous sodium bicarbonate
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated by evaporation under reduced pressure
  7. customto obtain a dark oil
  8. customThis oil was purified by careful column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-ee0683effdb7440db263893b06dafd16
Quelldatensatz
uspto-grants-1995_10
Patentnummer
US05461161

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