5-Aminovaleric acid → 4-(2-Oxopiperidinomethyl)-nitrobenzene

HRID 1374817

Reaktionsgleichung

Reaktionsgleichung von HRID 1374817
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[NH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=O.C([BH3-])#N.[Na+].Cl>CO.O>[O:19]=[C:17]1[CH2:16][CH2:15][CH2:14][CH2:13][N:12]1[CH2:8][C:7]1[CH:10]=[CH:11][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=1

Komponenten

7

Versuchsvorschrift

6.4 g (42 mmol) of 4-nitrobenzaldehyde are dissolved in 150 ml of methanol and combined with 4.9 g (42 mmol) of 5-aminovaleric acid and 1.8 g (29 mmol) of sodium cyanoborohydride. The mixture is stirred for 18 hours at ambient temperature and then carefully mixed with 20 ml of conc. hydrochloric acid. The solvent is eliminated in vacuo, the residue is taken up in water and extracted with dichloromethane. The residue obtained after evaporation is chromatographed on silica gel (dichloromethane/methanol, 4:1). A mixture of methyl 5-(4-nitrobenzylamino)-pentanoate and 4-(2-oxopiperidinomethyl)-nitrobenzene is obtained which is dissolved in 100 methanol and combined with 50 ml of 1 N sodium hydroxide solution. The mixture is stirred for one hour at ambient temperature, 50 ml of 1 N hydrochloric acid are added and the reaction solution is evaporated down to 100 ml. The aqueous phase thus obtained is extracted with dichloromethane. The combined organic phases are dried over sodium sulphate and evaporated to dryness.

Aufarbeitung

  1. extractionextracted with dichloromethane
  2. customThe residue obtained
  3. customafter evaporation
  4. customis chromatographed on silica gel (dichloromethane/methanol, 4:1)
  5. additionA mixture of methyl 5-(4-nitrobenzylamino)-pentanoate

Quellen und Nachweise

ORD-Eintrag
ord-975a988f6a744c18ac49fa4ca54dbc0b
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07166615B2

Verknüpfte Notizen

Wird geladen…