反応 #70451

ord-7373e526e63343878cd0b20258e7f221

反応方程式

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
収率 69.2%
C[C@H]1CN(c2ccc(C#N)cn2)CCN1
6-((S)-3-Methyl-piperazin-1-yl)-nicotinonitrile
収率 69.2%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the organic layer is separated
  2. 2
    乾燥dried over sodium sulfate
  3. 3
    濃縮concentrated under reduced pressure to a white residue
  4. 4
    その他The solid is further dried under high vacuum

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08536168B2uspto-grants-2013_09