Reaktionsgleichung
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][S:9]([C:12]2[CH:20]=[CH:19][C:15](C(O)=O)=[CH:14][CH:13]=2)(=[O:11])=[O:10])=[CH:4][C:3]=1[C:21]([F:24])([F:23])[F:22].Cl.[CH2:26]([O:28][C:29](=[O:35])[C@H:30]([C@@H:32]([CH3:34])[OH:33])[NH2:31])[CH3:27].O.[OH:37][C:38]1C2N=NNC=2C=CC=1.C(N(CC)CC)C.C1(N=C=NC2CCCCC2)CCCCC1>>[CH2:26]([O:28][C:29](=[O:35])[CH:30]([NH:31][C:38](=[O:37])[C:13]1[CH:14]=[CH:15][CH:19]=[CH:20][C:12]=1[S:9](=[O:11])(=[O:10])[NH:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[C:3]([C:21]([F:22])([F:24])[F:23])[CH:4]=1)[CH:32]([OH:33])[CH3:34])[CH3:27]Komponenten
6
Edukt 5
Produkt 1
Versuchsvorschrift
Under the conditions of Example 2(a), 3.633 g (10 mmol) of 4-[N-(4-Fluoro-3-trifluoromethylphenyl)sulfamoyl]benzoic acid, 1.736 g (10 mmol) of L-threonine ethyl ester hydrochloride, 1.531 g (10 mmol) of hydroxybenzotriazole, hydrate, as well as 1.012 g (10 mmol) of triethylamine and 2.063 g (10 mmol) of dicyclohexylcarbodiimide are reacted and worked up analogously. The crude product is chromatographed on silica gel. The title compound is eluted with ethyl acetate.
Aufarbeitung
- customThe crude product is chromatographed on silica gel
- washThe title compound is eluted with ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-97698e87395e4adf8687f2c0fbc7cbbd
- Quelldatensatz
- uspto-grants-1993_05
- Patentnummer
- US05210290
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