4-Methylmorpholine → N1-(2-amino-2-methylpropyl)-N2-phenylacetylglycinamide
Reaktionsgleichung
[C:1]1([CH2:7][C:8]([NH:10][CH2:11][C:12]([OH:14])=O)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CN1CCOCC1.ClC(OCC)=O.[NH2:28][CH2:29][C:30]([NH2:33])([CH3:32])[CH3:31].C(=O)([O-])[O-].[K+].[K+]>O.C(Cl)(Cl)Cl>[NH2:33][C:30]([CH3:32])([CH3:31])[CH2:29][NH:28][C:12](=[O:14])[CH2:11][NH:10][C:8](=[O:9])[CH2:7][C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Komponenten
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- -23 °C
Versuchsvorschrift
A mixture of phenylacetylglycine (10.0 g.), N-methyl morpholine (5.78 ml.) and chloroform (60 ml.) was stirred for 5 minutes. After cooling to -23° C., ethyl chloroformate (4.7 ml.) was added rapidly to the mixture during 1 minute, whereupon the temperture of the mixture rose to -15° C. After stirring for 1 minute, 1,2-diamino-2-methyl-propane (5.4 ml.) was added rapidly to the reaction mixture and the temperature was allowed to rise to room-temperature. After 1 hour at room temperature, the reaction mixture was poured into water (50 ml.) and the organic layer discarded. The aqueous layer was basified with excess potassium carbonate, and extracted with chloroform (4×100 ml.). The combined extracts were dried (MgSO4) and evaporated. Trituration and filtration of the solid residue with ether gave N1 -(2-amino-2-methylpropyl)-N2 -phenylacetylglycinamide as a solid (8.8 g.), m.p. 150°-155° C.
Aufarbeitung
- customrose to -15° C
- stirringAfter stirring for 1 minute
- waitAfter 1 hour at room temperature
- extractionextracted with chloroform (4×100 ml.)
- dry with materialThe combined extracts were dried (MgSO4)
- customevaporated
- filtrationTrituration and filtration of the solid residue with ether
Quellen und Nachweise
- ORD-Eintrag
- ord-8244ff0c080246bba8faaf64ab9b70dd
- Quelldatensatz
- uspto-grants-1981_12
- Patentnummer
- US04303649
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