Reaktion #2816

ord-09f79ec740dc49de8727d8657531ecd2

Reaktionsgleichung

CN
methylamine
OCCC#Cc1cccnc1
XII
OCCC#Cc1cccnc1
4-(3-Pyridinyl)-3-butyne-1-ol
CNCCC#Cc1cccnc1
XIII
CNCCC#Cc1cccnc1
N-Methyl-4-(3-pyridinyl)-3-butyne-1-amine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat 45° C
  2. 2
    Extraktionthe reaction mixture was extracted with chloroform (10×5 mL)
  3. 3
    TrocknenThe combined organic extracts were dried over anhydrous sodium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated
  6. 6
    SonstigeThe residue obtained
  7. 7
    Sonstigewas chromatographed on a silica gel column
  8. 8
    workup.ADDITIONwith a chloroform: methanol mixture containing 1% triethylamine as eluent

Vorschrift

An aqueous methylamine solution (5 mL, 40%, 58.7 mmole) was mixed with XII (200 mg, 0.08 mmole) and stirred for 3 hr. in a sealed tube at 45° C. After the reaction was complete, water (10 mL) was added to the cooled reaction mixture, and the reaction mixture was extracted with chloroform (10×5 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The residue obtained was chromatographed on a silica gel column using methanol:chloroform (1:9) and then with a chloroform: methanol mixture containing 1% triethylamine as eluent. About 70 mg of XIII was obtained as a slightly yellow syrup, which was distilled at 110°-112° C., 0.04 mm Hg. XIII was converted to its mono fumarate salt form, which exhibits a melting point of 103°-104° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731314uspto-grants-1998_03