Triethylamine → 6-((2R,5S)-2,5-Dimethyl-piperazin-1-yl)-nicotinonitrile

HRID 42175

Reaktionsgleichung

Reaktionsgleichung von HRID 42175
[CH3:1][C@H:2]1[CH2:7][NH:6][C@H:5]([CH3:8])[CH2:4][NH:3]1.Cl[C:10]1[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][N:11]=1.C(N(CC)CC)C>CN1CCCC1=O>[CH3:1][C@@H:2]1[CH2:7][NH:6][C@@H:5]([CH3:8])[CH2:4][N:3]1[C:10]1[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][N:11]=1

Komponenten

5

Edukt 3

HCID 8471TriethylamineHCID 2206722,5-Dimethylpiperazine, trans-HCID 51520946-Chloro-3-pyridinecarbonitrile

Produkt 1

HCID 574716106-((2R,5S)-2,5-Dimethyl-piperazin-1-yl)-nicotinonitrileAusbeute 9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 13387N-methyl-2-pyrrolidoneLösungsmittel

Versuchsvorschrift

Combine (2S,5R)-2,5-dimethyl-piperazine (200 mg, 1.75 mmol), 6-chloro-nicotinonitrile (1.75 mmol) and triethylamine (5.25 mmol) in a 0.875 M solution of 1-methyl-2-pyrrolidinone. Microwave reaction mixture for 30 min at 150° C. Partition between ethyl acetate and water, collecting organic phase. Wash aqueous layer again with ethyl acetate and combine organics. Dry with sodium sulfate, filter and concentrate. Purify on preparative HPLC to give the title compound. (9% yield)

Aufarbeitung

  1. customMicrowave reaction mixture for 30 min at 150° C
  2. customPartition between ethyl acetate and water
  3. customcollecting organic phase
  4. dry with materialDry with sodium sulfate
  5. filtrationfilter
  6. concentrationconcentrate
  7. customPurify on preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-bc5f400ac57641de862139b65cf0bb17
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08536168B2

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