Reaktionsgleichung
C([O:5][C:6](=[O:39])[C@@H:7]([NH:29][S:30]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)(=[O:32])=[O:31])[CH2:8][NH:9][C:10](=[O:28])[C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][NH:20]C(OC(C)(C)C)=O)=[CH:13][CH:12]=1)(C)(C)C.O1CCOCC1.[ClH:46]>>[ClH:46].[NH2:20][CH2:19][CH2:18][O:17][C:14]1[CH:15]=[CH:16][C:11]([C:10]([NH:9][CH2:8][C@H:7]([NH:29][S:30]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)(=[O:32])=[O:31])[C:6]([OH:39])=[O:5])=[O:28])=[CH:12][CH:13]=1Komponenten
4
Versuchsvorschrift
A suspension of 2-3 (105 mg, 0.19 mmol) in 6N HCl (5 mL) was treated with dioxane (5 mL) to effect a homogeneous solution. After stirring for 20 h at ambient temperature, the solvents were evaporated and the resulting residue azeotroped with toluene to afford 12-1 as a colorless solid.
Aufarbeitung
- customthe solvents were evaporated
- customthe resulting residue azeotroped with toluene
Quellen und Nachweise
- ORD-Eintrag
- ord-3545c1a839b84107a6729d4bc39d022f
- Quelldatensatz
- uspto-grants-1999_07
- Patentnummer
- US05929120
Verknüpfte Notizen
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