Dicyclohexylcarbodiimide → (S)-Benzyl 2-(dimethylcarbamoyl)pyrrolidine-1-carboxylate

HRID 1285001

Reaktionsgleichung

Reaktionsgleichung von HRID 1285001
[CH2:1]([O:8][C:9]([N:11]1[CH2:18][CH2:17][CH2:16][C@H:12]1[C:13](O)=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1C=CC2N(O)N=NC=2C=1.C1CC[CH:32]([N:35]=[C:36]=NC2CCCCC2)CC1.O1CCCC1.CNC>C1COCC1.C(OCC)(=O)C>[CH2:1]([O:8][C:9]([N:11]1[CH2:18][CH2:17][CH2:16][C@H:12]1[C:13]([N:35]([CH3:36])[CH3:32])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

7

Edukt 4

HCID 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 101987Benzyloxycarbonyl-L-prolineHCID 22320367Dimethylamine tetrahydrofuran

Produkt 1

HCID 13564352(S)-Benzyl 2-(dimethylcarbamoyl)pyrrolidine-1-carboxylateAusbeute 88,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

In 80 ml of dry THF were dissolved 4.9 g (20 m mol) of N-benzyloxycarbonyl-L-proline (29) and 3.5 g (26 m mole) of HOBT and then 4.53 g (22 m mol) of DCC was slowly added to the solution at 0° C. After stirring the mixture for 30 minutes at the same temperature, 10 ml of solution of 2M dimethylamine tetrahydrofuran was added. The resulting mixture was allowed to stand for 12 hours at room temperature. THF was distilled off from the reaction mixture under reduced pressure, the residue thus formed was dissolved in 200 ml of ethyl acetate, and the solution was washed, in succesion, with 75 ml of an aqueous solution of 0.5N hydrochloric acid, 75 ml of a saturated aqueous sodium hydrogencarbonate solution, and 50 ml of water. After drying the organic layer with anhydrous magnesium sulfate, ethyl acetate was distilled off and the residue thus formed was purified by silica gel column chromatography (400 ml of Wako gel C-200, ethyl acetate) to provide 4.8 g of (S)-1-benzyloxycarbonyl-N,N-dimethyl-2-pyrrolidinecarboxamide (88) having a melting point of 66°-67° C.

Aufarbeitung

  1. additionwas added
  2. distillationTHF was distilled off from the reaction mixture under reduced pressure
  3. customthe residue thus formed
  4. washthe solution was washed, in succesion, with 75 ml of an aqueous solution of 0.5N hydrochloric acid, 75 ml of a saturated aqueous sodium hydrogencarbonate solution, and 50 ml of water
  5. dry with materialAfter drying the organic layer with anhydrous magnesium sulfate, ethyl acetate
  6. distillationwas distilled off
  7. customthe residue thus formed
  8. customwas purified by silica gel column chromatography (400 ml of Wako gel C-200, ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-b2fa269d95504e74b9b3fe3c39d34b28
Quelldatensatz
uspto-grants-1986_01
Patentnummer
US04564609

Verknüpfte Notizen

Wird geladen…