Reaktionsgleichung
C([O:5][C:6](=[O:48])[CH:7]([NH:14][C:15](=[O:47])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[S:22][S:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[C:30](=[O:46])[NH:31][CH:32]([C:39]([O:41]C(C)(C)C)=[O:40])[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)(C)(C)C.ClCCl.FC(F)(F)C(O)=O>CCOCC.CCCCCC>[C:6]([CH:7]([NH:14][C:15]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[S:22][S:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[C:30]([NH:31][CH:32]([C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1)[C:39]([OH:41])=[O:40])=[O:46])=[O:47])[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([OH:48])=[O:5]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
This compound was prepared according to the procedure described in Example 50 using [R-(R*,R,)] (2-{2-[(tert-butoxycarbonyl-phenyl-methyl)-carbamoyl]phenyldisulfanyl}-benzoylamino)-phenyl-acetic acid tert-butyl ester (0.2 g, 0.3 mmol) from Example 38, 10 mL dichloromethane, and 10 mL trifluoroacetic acid. The crude product was stirred with ether/hexane and filtered to afford 73.0 mg of the title compound, mp 231°-232° C.
Aufarbeitung
- customThis compound was prepared
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-09afff73385444c29d7f2be986c88092
- Quelldatensatz
- uspto-grants-1997_09
- Patentnummer
- US05668291
Verknüpfte Notizen
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