Reaktionsgleichung
[NH:1]1[CH2:6][CH2:5][C:4](=[C:7]2[C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[CH2:11][CH2:10][C:9]3[CH:18]=[CH:19][CH:20]=[CH:21][C:8]2=3)[CH2:3][CH2:2]1.Cl.[N:23]1[CH:28]=[CH:27][C:26]([CH2:29][C:30](O)=[O:31])=[CH:25][CH:24]=1.C1C=CC2N(O)N=NC=2C=1>CN(C=O)C>[N:23]1[CH:28]=[CH:27][C:26]([CH2:29][C:30]([N:1]2[CH2:2][CH2:3][C:4](=[C:7]3[C:8]4[CH:21]=[CH:20][CH:19]=[CH:18][C:9]=4[CH2:10][CH2:11][C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][C:13]3=4)[CH2:5][CH2:6]2)=[O:31])=[CH:25][CH:24]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Dissolve 0.15 g (0.6 m mole) of 10,11-dihydro-5-(4-piperidylidene)-5H-dibenzo[a,d]cycloheptene, 0.096 g (0.55 m mole) of 4-pyridylacetic acid hydrochloride, 0.16 g (0.83 m mole) of DEC and 0.075 g (0.55 m mole) of HOBT in 5 mL of DMF and stir at room temperature for 18 hours under nitrogen. Concentrate under vacuo and partition between 100 mL each of EtOAc and 10% aqueous sodium hydrogenphosphate. Dry the organic layer over MgSO4 and concentrate under vacuo. The resulting residue is chromatographed on silica gel using 98% dichloro methane and 2% MeOH, saturated with ammonia as the solvent, giving the product as a white waxy solid, mp=162.8°-163.4° C.
Aufarbeitung
- concentrationConcentrate under vacuo
- custompartition between 100 mL each of EtOAc and 10% aqueous sodium hydrogenphosphate
- dry with materialDry the organic layer over MgSO4
- concentrationconcentrate under vacuo
- customThe resulting residue is chromatographed on silica gel using 98% dichloro methane and 2% MeOH, saturated with ammonia as the solvent
- customgiving the product as a white waxy solid, mp=162.8°-163.4° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-55ba33b294a944578b799c6f726e633d
- Quelldatensatz
- uspto-grants-1998_02
- Patentnummer
- US05714609
Verknüpfte Notizen
Wird geladen…