Reaktionsgleichung
[NH2:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4].C(N(CC)CC)C.FC(F)(F)C([N:19]([CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH3:51])[C:20]1[CH:35]=[CH:34][C:23]([C:24](ON2C(=O)CCC2=O)=[O:25])=[CH:22][CH:21]=1)=O.[OH-].[Na+]>O.C(O)C>[CH2:36]([NH:19][C:20]1[CH:21]=[CH:22][C:23]([C:24]([NH:1][C:2]([CH3:7])([CH3:6])[C:3]([OH:5])=[O:4])=[O:25])=[CH:34][CH:35]=1)[CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH3:51]Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a stirred solution of 103 mg. of 2-aminoisobutyric acid and 4.5 ml. of triethylamine in 1.5 ml. of water is added a solution of 550 mg. of N-[N-trifluoroacetyl-4-(hexadecylamino)benzoyloxy]succinimide in 4.5 ml. of ethanol. The mixture is stirred for 23 hours at room temperature, treated with 2 ml. of 2N sodium hydroxide solution, and then acidified. The mixture is diluted with water and then filtered. Recrystallization from ether-hexane affords the title compound as a white solid.
Aufarbeitung
- additiontreated with 2 ml
- filtrationfiltered
- customRecrystallization from ether-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-28b5aee9d0e04b4d954528db4260888d
- Quelldatensatz
- uspto-grants-1979_01
- Patentnummer
- US04136256
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