4-Methylmorpholine → Ethyl 2-(2-((tert-butoxycarbonyl)amino)propanamido)-3-oxobutanoate

HRID 1930111Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1930111
CN1CCOCC1.[C:8]([O:12][C:13]([NH:15][CH:16]([CH3:20])[C:17]([OH:19])=O)=[O:14])([CH3:11])([CH3:10])[CH3:9].ClC(OCC(C)C)=O.S(C1C=CC(C)=CC=1)(O)(=O)=O.[NH2:40][CH:41]([C:47](=[O:49])[CH3:48])[C:42]([O:44][CH2:45][CH3:46])=[O:43]>C1COCC1>[C:8]([O:12][C:13]([NH:15][CH:16]([CH3:20])[C:17]([NH:40][CH:41]([C:47](=[O:49])[CH3:48])[C:42]([O:44][CH2:45][CH3:46])=[O:43])=[O:19])=[O:14])([CH3:9])([CH3:10])[CH3:11]

Komponenten

6

Edukt 4

HCID 79724-Methylmorpholine2×HCID 62365Isobutyl chloroformateHCID 2684712-N-Boc-aminopropionic acidHCID 86636663Butanoic acid, 2-amino-3-oxo-, ethyl ester, 4-methylbenzenesulfonate (1:1)

Produkt 1

HCID 57992159Ethyl 2-(2-((tert-butoxycarbonyl)amino)propanamido)-3-oxobutanoateAusbeute 68,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
-25 °C

Versuchsvorschrift

A solution of 4-methylmorpholine (900 g) in THF (15 L) was added to 2-(tert-butoxycarbonylamino)propanoic acid (1690 g, 8933.17 mmol). The mixture was cooled to −25° C. and isobutyl chloroformate (1.164 L, 8933.17 mmol) was added. After 20 minutes the second equivalent of 4-methylmorpholine (900 g) was added followed by ethyl 2-amino-3-oxobutanoate Tosylate salt (see J-P. Genet et al, Eur. J. Org. Chem., 2004, 3017-3026) (2700 g, 8507.78 mmol) suspended in THF (2.5 L). The mixture was stirred at −25° C. for 30 minutes and then left to warm to ambient temperature overnight. The reaction was quenched with water (15 L), extracted with EtOAc (3×5 L) and the combined extracts washed with 50% saturated brine (5 L). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 50 to 80% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford ethyl 2-(2-(tert-butoxycarbonylamino)propanamido)-3-oxobutanoate (1850 g, 68.7%).

Aufarbeitung

  1. waitleft
  2. temperatureto warm to ambient temperature overnight
  3. customThe reaction was quenched with water (15 L)
  4. extractionextracted with EtOAc (3×5 L)
  5. washthe combined extracts washed with 50% saturated brine (5 L)
  6. dry with materialThe organic layer was dried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customto afford crude product
  10. customThe crude product was purified by flash silica chromatography, elution gradient 50 to 80% EtOAc in isohexane
  11. customPure fractions were evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-ec8584dd9c77493fbd3557fc79beef21
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08188092B2

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