Methanol → HCID 20144947, Verbindung
Reaktionsgleichung
O1[C:5](=O)[CH:4]=[NH+:3][N-]1.C([C:9]1[C:13](=[O:14])O[N-][N+:10]=1[CH3:15])=O.N/[C:17](/[CH3:23])=[CH:18]\[C:19](OC)=O.[C:24](OC)(=O)[CH2:25]C(C)=O.C[OH:33]>>[C:17]1([C:5]2[O:14][C:13]([CH2:9][NH:10][CH:15]=[O:33])=[N:3][CH:4]=2)[CH:23]=[CH:25][CH:24]=[CH:19][CH:18]=1Komponenten
5
Versuchsvorschrift
To 0.78 g (5 mmol) 2-pyridine-N-oxide carboxaldehyde (1) in 15 ml methanol was added 0.58 g (5 mmol) methyl 3-aminocrotonate and 0.58 g (5 mmol) methyl acetoacetate and the resulting solution was refluxed for 18 hours. The cooled reaction mixture was filtered to give a yellow solid that was triturated with hexane to give pure (2), m.p. 225°-228°.
Aufarbeitung
- temperaturethe resulting solution was refluxed for 18 hours
- customThe cooled reaction mixture
- filtrationwas filtered
- customto give a yellow solid
- customthat was triturated with hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-abc5a1c0339a4f79895802651dcf62c8
- Quelldatensatz
- uspto-grants-1988_04
- Patentnummer
- US04735956
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