Parabanic acid → HCID 22174530, Verbindung
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[CH3:23])=[O:16])=[C:11]([Cl:24])[CH:10]=2)=[C:4]([CH2:25][O:26][CH2:27][CH2:28]O)[CH:3]=1.[C:30]1([NH:37][C:35](=[O:36])[NH:34][C:32]1=[O:33])=[O:31]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[CH3:23])=[O:16])=[C:11]([Cl:24])[CH:10]=2)=[C:4]([CH:3]=1)[CH2:25][O:26][CH2:27][CH2:28][N:34]1[C:32](=[O:33])[C:30](=[O:31])[NH:37][C:35]1=[O:36]Komponenten
3
Versuchsvorschrift
Compound 158 (47 mg, 0.1 mmol) and parabanic acid (16 mg, 0.14 mmol) were treated as described in the preparation of compound 219. Purification was done by flash chromatography (CH2Cl2/ethyl acetate 4:1) to provide the title compound, which was impure. The product was further purified by preparative TLC (CH2Cl2/ethyl acetate 20:1) to furnish the title compound as yellow oil.
Aufarbeitung
- customPurification
Quellen und Nachweise
- ORD-Eintrag
- ord-8b5f0d860ff944248aa6200d56379d4d
- Quelldatensatz
- uspto-grants-2006_04
- Patentnummer
- US07034015B2
Notizen zur Reaktion
Wird geladen…