4,7-Dihydro-4,7-dioxo-6-ethoxy-1-ethyl-1H-cyclohepta[b]pyridine-2-carboxylic Acid → 4,7-Dihydro-4,7-dioxo-6-ethoxy-1H-cyclohepta[b]pyridine-2-carboxylic Acid
Reaktionsgleichung
[O:1]=[C:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[N:5](CC)[C:4]2[CH:13]=[CH:14][C:15](=[O:21])[C:16]([O:18][CH2:19][CH3:20])=[CH:17][C:3]1=2>Cl>[O:1]=[C:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[NH:5][C:4]2[CH:13]=[CH:14][C:15](=[O:21])[C:16]([O:18][CH2:19][CH3:20])=[CH:17][C:3]1=2Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 4,7-dihydro-4,7-dioxo-6-ethoxy-1-ethyl-1H-cyclohepta[b]pyridine-2-carboxylic acid (5.3 g, described in Example 13) and 19% hydrochloric acid (50 ml) is refluxed for 1 hr and cooled to room temperature. The precipitate is collected and washed with water to give the title compound, mp > 280° C.
Aufarbeitung
- temperatureis refluxed for 1 hr
- customThe precipitate is collected
- washwashed with water
Quellen und Nachweise
- ORD-Eintrag
- ord-813ce1290e1f401783c37957ab593ba6
- Quelldatensatz
- uspto-grants-1978_12
- Patentnummer
- US04130649
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