Hydrochloric Acid → HCID 178425411, Verbindung

HRID 275042

Reaktionsgleichung

Reaktionsgleichung von HRID 275042
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([SH:7])[N:3]=1.C(OC(=O)C)(=[O:10])C.ClCl.Cl[C:18]1[C:24]([CH3:25])=[CH:23][CH:22]=[C:21]([Cl:26])[C:19]=1[NH2:20].[ClH:27].[OH2:28]>C(O)(=O)C>[Cl:27][C:18]1[C:24]([CH3:25])=[CH:23][CH:22]=[C:21]([Cl:26])[C:19]=1[NH:20][S:7]([C:4]1[N:3]=[C:2]([NH2:1])[NH:6][N:5]=1)(=[O:10])=[O:28]

Komponenten

8

Edukt 6

HCID 313Hydrochloric AcidHCID 962WaterHCID 7918Acetic AnhydrideHCID 24526ChlorineHCID 1165292,6-Dichloro-3-methylanilineHCID 178509066HCID 178509066, Verbindung

Produkt 1

HCID 178425411HCID 178425411, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel2×

Reaktionsbedingungen

Temperatur
12 °C

Versuchsvorschrift

A mixture of 11.6 g (0.10 mole) of 5-amino-3-mercapto-1,2,4-triazole, 12.75 g (0.0125 moles) of acetic anhydride and 100 ml of acetic acid was prepared and heated at reflux with stirring for 12 hours. Another 50 ml of acetic acid and 10 ml of water were then added and the mixture was cooled to 12° C. Chlorine (21 g, 0.3 mole) was then added to the mixture with stirring over a 15 min. period at 12°-20° C. A yellow solution was obtained. About 100 ml of volatiles were removed by distillation at 50° C. under reduced pressure. The resulting residue was combined with 2,6-dichloro-3-methylaniline (14.1 g, 0.080 mole) and the mixture heated at 115° C. for 4 hours with stirring. Concentrated aqueous hydrochloric acid (50 ml) was then added and the mixture was heated at reflux with stirring for another 5 hours. It was then allowed to cool to ambient temperature and the solids present were collected by filtration. The collected solids were placed in 200 ml of 10 percent aqueous sodium hydroxide. The insoluble material was removed by filtration and the pH of the filtrate was adjusted to 4.5 with hydrochloric acid to reprecipitate the title compound. The solids were recovered by filtration, washed with water, and dried under reduced pressure to obtain 10.1 g (28.9 percent of theory) of the title compound assaying 95 percent by high pressure liquid chromatography.

Aufarbeitung

  1. customwas prepared
  2. temperatureheated
  3. temperatureat reflux
  4. stirringwith stirring over a 15 min. period at 12°-20° C
  5. customA yellow solution was obtained
  6. customAbout 100 ml of volatiles were removed by distillation at 50° C. under reduced pressure
  7. temperaturethe mixture heated at 115° C. for 4 hours
  8. stirringwith stirring
  9. temperaturethe mixture was heated
  10. temperatureat reflux
  11. stirringwith stirring for another 5 hours
  12. temperatureto cool to ambient temperature
  13. filtrationthe solids present were collected by filtration
  14. customThe insoluble material was removed by filtration
  15. filtrationThe solids were recovered by filtration
  16. washwashed with water
  17. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-1a35c5ae88114c1da25b6c61355db467
Quelldatensatz
uspto-grants-1995_02
Patentnummer
US05391759

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