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5-Amino-2-chloropyridine → 6-chloro-N-methylpyridin-3-amine

HRID 1585008
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1585008
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:8])=[N:6][CH:7]=1.[CH:9]([O-])([O-])OCC>>[Cl:8][C:5]1[CH:4]=[CH:3][C:2]([NH:1][CH3:9])=[CH:7][N:6]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 793055-Amino-2-chloropyridineHCID 53630039Ethylorthoformate

Produkt 1

HCID 155151186-chloro-N-methylpyridin-3-amine

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

To 5.0 g (0.039 mole) of 5-amino-2-chloropyridine was added 40 ml of ethyl orthoformate and the mixture was refluxed for 5 hours. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in 50 ml of EtOH. After addition of 1.8 g of sodium borohydride, the mixture was stirred at 70-80° C. for 3 hours. The reaction mixture was concentrated and after addition of 50 ml of iced water and 5 ml of concentrated hydrochloric acid, the mixture was adjusted to pH 7-8 with NaHCO3 and extracted with AcOEt (50 ml×3). The AcOEt layers were pooled, washed with water and dried over MgSO4. The AcOEt was distilled off and hexane was added to the crystalline residue. The crystals are collected by filtration, washed with hexane and dried to give 5.1 g of the title compound as white crystals.

Aufarbeitung

  1. temperaturethe mixture was refluxed for 5 hours
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. dissolutionthe residue was dissolved in 50 ml of EtOH
  4. additionAfter addition of 1.8 g of sodium borohydride
  5. concentrationThe reaction mixture was concentrated
  6. additionafter addition of 50 ml of iced water and 5 ml of concentrated hydrochloric acid
  7. extractionextracted with AcOEt (50 ml×3)
  8. washwashed with water
  9. dry with materialdried over MgSO4
  10. distillationThe AcOEt was distilled off
  11. additionhexane was added to the crystalline residue
  12. filtrationThe crystals are collected by filtration
  13. washwashed with hexane
  14. customdried

Quellen und Nachweise

ORD-Eintrag
ord-1aa976f4d75f46708dcd060c090a96b3
Quelldatensatz
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05935981

Notizen zur Reaktion

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