1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-[(R)-1-{3-(1-tert-butoxycarbonyl-4-piperidyl)propionyl}-3-piperidylcarbonyl]-3-ethynyl-beta-alanine ethyl ester

HRID 843733Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 843733
Cl.NC[CH:4](C#C)[C:5]([O:7][CH2:8][CH3:9])=[O:6].[C:12]([O:16][C:17]([N:19]1[CH2:24][CH2:23][CH:22]([CH2:25][CH2:26][C:27]([N:29]2[CH2:34][CH2:33][CH2:32][C@@H:31](C(O)=O)[CH2:30]2)=[O:28])[CH2:21][CH2:20]1)=[O:18])([CH3:15])([CH3:14])[CH3:13].[OH:38]N1C2C=CC=CC=2N=N1.C(N=C=N[CH2:53][CH2:54][CH2:55][N:56]([CH3:58])C)C>CN(C)C=O.O>[CH2:8]([O:7][C:5](=[O:6])[CH2:4][CH:55]([C:54]#[CH:53])[NH:56][C:58]([C@@H:31]1[CH2:32][CH2:33][CH2:34][N:29]([C:27](=[O:28])[CH2:26][CH2:25][CH:22]2[CH2:21][CH2:20][N:19]([C:17]([O:16][C:12]([CH3:13])([CH3:14])[CH3:15])=[O:18])[CH2:24][CH2:23]2)[CH2:30]1)=[O:38])[CH3:9]

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a mixture of ethyl 3-amino-2-ethynylpropionate hydrochloride (0.5 g), (R)-1-[3-(1-tert-butoxycarbonyl-4-piperidyl)propionyl]-3-piperidinecarboxylic acid (1.04 g) and 1-hydroxybenztriazole (0.38 g) in N,N-dimethylformamide (5 ml) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (0.51 ml) under stirring at 0° C. After stirring at ambient temperature overnight, the mixture was poured into water and extracted with ethyl acetate. The extract was washed with water, brine and dried over MgSO4, and evaporated in vacuo. The residue was purified by chromatography on silica gel eluting with CHCl3:MeOH=(100:1) to give N-[(R)-1-{3-(1-tert-butoxycarbonyl-4-piperidyl)propionyl}-3-piperidylcarbonyl]-3-ethynyl-β-alanine ethyl ester as an oil (1.38 g).

Aufarbeitung

  1. stirringAfter stirring at ambient temperature overnight
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with water, brine
  4. dry with materialdried over MgSO4
  5. customevaporated in vacuo
  6. customThe residue was purified by chromatography on silica gel eluting with CHCl3

Quellen und Nachweise

ORD-Eintrag
ord-d7c9d268afa44dc3a8129143b0ad6cff
Quelldatensatz
uspto-grants-2002_04
Patentnummer
US06380215B1

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