Ammonium Acetate → (S)-N-{3-[4-(4-(1-Cyano-cyclopropylmethylidene)-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

HRID 750932

Reaktionsgleichung

Reaktionsgleichung von HRID 750932
O=C1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:18][C@H:17]([CH2:19][NH:20][C:21](=[O:23])[CH3:22])[O:16][C:15]3=[O:24])=[CH:10][C:9]=2[F:25])[CH2:4][CH2:3]1.[CH:26]1([CH2:29][C:30]#N)[CH2:28][CH2:27]1.[C:32]([O-])(=O)C.[NH4+:36]>C1(C)C=CC=CC=1>[C:32]([C:26]1([CH:29]=[C:30]2[CH2:7][CH2:6][N:5]([C:8]3[CH:13]=[CH:12][C:11]([N:14]4[CH2:18][C@H:17]([CH2:19][NH:20][C:21](=[O:23])[CH3:22])[O:16][C:15]4=[O:24])=[CH:10][C:9]=3[F:25])[CH2:4][CH2:3]2)[CH2:27][CH2:28]1)#[N:36]

Komponenten

5

Versuchsvorschrift

The mixture of (S)-N-{3-[4-(4-oxo-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide (2.86 mmol), cyclopropylacetonitrile (5.73 mmol), ammonium acetate (catalytic) in 100 ml of toluene was heated at reflux temperature for 5 to 6 hours. The reaction mixture was cooled to room temperature and extracted with ethyl acetate water mixture, dried and evaporated to give crude product. The crude product was recrystallized from ethyl acetate to furnish title compound in 69% yield.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat reflux temperature for 5 to 6 hours
  3. extractionextracted with ethyl acetate water mixture
  4. customdried
  5. customevaporated
  6. customto give crude product
  7. customThe crude product was recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-9afbb5837de94abc90f0dfb3b34b7efb
Quelldatensatz
uspto-grants-2008_07
Patentnummer
US07405228B2

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