Dicyclohexylcarbodiimide → N-(1-Carboxyethyl)-L-alanyl-L-proline

HRID 2418411Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2418411
C(C(N[C@H](C(O)=O)C)C)(OCC1C=CC=CC=1)=O.Cl.C(OC(=O)[C@@H]1CCCN1)C1C=CC=CC=1.C1(N=C=NC2CCCCC2)CCCCC1.[C:50]([CH:60]([NH:62][C@H:63]([C:65]([N:67]1[CH2:74][CH2:73][CH2:72][C@H:68]1[C:69]([OH:71])=[O:70])=[O:66])[CH3:64])[CH3:61])([O:52]CC1C=CC=CC=1)=[O:51]>N1C=CC=CC=1.C(N(CC)CC)C>[C:50]([CH:60]([NH:62][C@H:63]([C:65]([N:67]1[CH2:74][CH2:73][CH2:72][C@H:68]1[C:69]([OH:71])=[O:70])=[O:66])[CH3:64])[CH3:61])([OH:52])=[O:51]

Komponenten

7

Versuchsvorschrift

Dissolve 0.75 g of N-(1-carbobenzoxyethyl)-L-alanine in pyridine and add 7.5 ml of 1M triethylamine in pyridine. Cool, and add 1.09 g L-proline benzyl ester hydrochloride and 0.678 g dicyclohexylcarbodiimide. Store at 0° C. for 20 hours. Filter, then concentrate the reaction mixture in vacuo. Dissolve the residue in ethyl acetate and wash this solution with saturated K2CO3, then brine. Dry the organic phase, concentrate in vacuo, then chromatograph the residue on silica gel with ethyl acetate-hexane to isolate the diastereoisomeric mixture of N-(1-carbobenzoxyethyl)-L-alanyl-L-proline.

Aufarbeitung

  1. temperatureCool
  2. filtrationFilter
  3. concentrationconcentrate the reaction mixture in vacuo
  4. dissolutionDissolve the residue in ethyl acetate
  5. washwash this solution with saturated K2CO3
  6. customDry the organic phase
  7. concentrationconcentrate in vacuo
  8. customchromatograph the residue on silica gel with ethyl acetate-hexane to isolate

Quellen und Nachweise

ORD-Eintrag
ord-ae4272277d824605abc03a06461be78b
Quelldatensatz
uspto-grants-1984_09
Patentnummer
US04472380

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