Reaktion #70451

ord-7373e526e63343878cd0b20258e7f221

Reaktionsgleichung

CCN(CC)CC.Cl
triethylamine hydrochloride
CCN(CC)CC
Triethylamine
N#Cc1ccc(Cl)nc1
6-chloro-nicotinonitrile
C[C@H]1CNCCN1
(S)-2-methyl-piperazine
C[C@H]1CN(c2ccc(C#N)cn2)CCN1
desired product
Ausbeute 69.2%
C[C@H]1CN(c2ccc(C#N)cn2)CCN1
6-((S)-3-Methyl-piperazin-1-yl)-nicotinonitrile
Ausbeute 69.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe organic layer is separated
  2. 2
    Trocknendried over sodium sulfate
  3. 3
    Einengenconcentrated under reduced pressure to a white residue
  4. 4
    SonstigeThe solid is further dried under high vacuum

Vorschrift

Triethylamine (4.13 g, 3 mL, 40.8 mmol, 4 eq) is added to a solution of 6-chloro-nicotinonitrile (1.38 g, 10 mmol, 1 eq), (S)-2-methyl-piperazine (1.00 g, 10 mmol, 1 eq) in DMF (15 mL), and the resulting solution is stirred at rt for 14 h. A white precipitate of triethylamine hydrochloride forms in the course of the reaction. Water (15 mL) and EtOAc (100 mL) are added, the organic layer is separated, dried over sodium sulfate and concentrated under reduced pressure to a white residue. The solid is further dried under high vacuum to yield the desired product as a white solid (1.4 g, 69%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08536168B2uspto-grants-2013_09