Reaktionsgleichung
Cl[C:2]1[N:7]=[N:6][C:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:4][CH:3]=1.[N-:13]=[C:14]=[O:15].[K+].[C:17]([OH:21])([CH3:20])([CH3:19])[CH3:18].COCCOCCOC>CN(C=O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:17]([O:21][C:14]([NH:13][C:2]1[N:7]=[N:6][C:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:4][CH:3]=1)=[O:15])([CH3:20])([CH3:19])[CH3:18]Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of ethyl 6-chloro-3-pyridazine carboxylate (6.5 g) [British patent number 856, 409], potassium isocyanate (3.5 g), tert-butanol (6.0 ml), tetrakis(triphenylphosphine)palladium (400 mg) and diglyme (6 ml) in DMF (50 ml) was heated at reflux for 2 hours, cooled and partitioned between diethyl ether and water. The organic layer was dried (MgSO4), filtered through silica gel and evaporated. The resulting solid was purified by crystallisation from iso-hexane to give ethyl 6-(tert-butoxycarbonylamino)-3-pyridazine carboxylate (2.4 g), mp 87°-88° C.
Aufarbeitung
- temperaturewas heated
- temperatureat reflux for 2 hours
- temperaturecooled
- custompartitioned between diethyl ether and water
- dry with materialThe organic layer was dried (MgSO4)
- filtrationfiltered through silica gel
- customevaporated
- customThe resulting solid was purified by crystallisation from iso-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-cb5abc9447dc4bcd929602a6aed871a5
- Quelldatensatz
- uspto-grants-1998_12
- Patentnummer
- US05843942
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