1,2-Dichloroethane → HCID 131727147, Verbindung
Reaktionsgleichung
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:24]([OH:26])=O)[CH2:13][CH2:14][CH2:15][NH:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:27]([O:31][C:32](=[O:39])[NH:33][CH2:34][CH:35]([OH:38])[CH2:36][NH2:37])([CH3:30])([CH3:29])[CH3:28].C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1>CN(C)C=O>[CH2:1]([O:8][C:9](=[O:10])[NH:11][C@H:12]([C:24]([NH:37][CH2:36][CH:35]([OH:38])[CH2:34][NH:33][C:32]([O:31][C:27]([CH3:29])([CH3:28])[CH3:30])=[O:39])=[O:26])[CH2:13][CH2:14][CH2:15][NH:16][C:17]([O:19][C:20]([CH3:21])([CH3:22])[CH3:23])=[O:18])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Preparation takes place in analogy to Example 79A from 300 mg (0.82 mmol) of N2-[(benzyloxy)carbonyl]-N5-(tert-butoxycarbonyl)-L-ornithine and 202 mg (1.06 mmol) of tert-butyl(3-amino-2-hydroxypropyl)carbamate in 6 ml of dimethylformamide with the addition of 204 mg (1.06 mmol) of EDC and 33 mg (0.25 mmol) of HOBt.
Aufarbeitung
- customPreparation
Quellen und Nachweise
- ORD-Eintrag
- ord-287500946745438cb232d3f2a03e0e04
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07446102B2
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