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Hydrochloric Acid → (6-Chloro-2-methylpyridin-3-YL)methanamine

HRID 241689
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 241689
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([CH3:10])[N:3]=1.[BH4-].[Na+].B(F)(F)F.Cl>C1COCC1.CO>[Cl:1][C:2]1[N:3]=[C:4]([CH3:10])[C:5]([CH2:6][NH2:7])=[CH:8][CH:9]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 6356Boron trifluorideHCID 4311764Sodium borohydrideHCID 123877376-Chloro-2-methylnicotinonitrile

Produkt 1

HCID 59534442(6-Chloro-2-methylpyridin-3-YL)methanamine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887Methanol
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 6-Chloro-2-methyl-nicotinonitrile (6 g) in THF (120 ml) at 25° C. was added NaBH4 (3 g) followed by the dropwise addition of BF3 etherate (6 ml). The reaction mixture was stirred for 3 h. MeOH (100 ml) and 2N HCl (100 ml) was added and refluxed for 1 h. The organic solvent was removed in vacuum and conc. NaOH (40 ml) was added followed by extraction with diethyl ether. The organic layer was separated, dried and concentrated in vacuum followed by filtration over silica gel (EtOAc/MeOH 80:20). The title compound was crystallized from MeOH/HCl (5.5 g)

Aufarbeitung

  1. temperaturerefluxed for 1 h
  2. customThe organic solvent was removed in vacuum and conc. NaOH (40 ml)
  3. additionwas added
  4. extractionfollowed by extraction with diethyl ether
  5. customThe organic layer was separated
  6. customdried
  7. concentrationconcentrated in vacuum
  8. filtrationfollowed by filtration over silica gel (EtOAc/MeOH 80:20)
  9. customThe title compound was crystallized from MeOH/HCl (5.5 g)

Quellen und Nachweise

ORD-Eintrag
ord-5b72cf9b45d1488ab094354e00ccb3ff
Quelldatensatz
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08653075B2

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