HCID 178498786, Verbindung → methyl 7-amino-4H-5-oxa-3,9b-diazacyclopenta[a]naphthalene-6-carboxylate
Reaktionsgleichung
[NH2:1][C:2]1[CH:18]=[CH:17][C:5]2[N:6]=[C:7]([NH:10][CH2:11][CH:12](OC)OC)[CH2:8][O:9][C:4]=2[C:3]=1[C:19]([O:21][CH3:22])=[O:20]>Cl.CO>[NH2:1][C:2]1[CH:18]=[CH:17][C:5]2[N:6]3[CH:12]=[CH:11][N:10]=[C:7]3[CH2:8][O:9][C:4]=2[C:3]=1[C:19]([O:21][CH3:22])=[O:20]Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of methyl 7-amino-3-(2,2-dimethoxyethylamino)-2H-benzo[1,4]oxazine-8-carboxylate (Intermediate 27, 0.910 g) in concentrated aqueous hydrochloric acid (8 mL) and methanol (10 mL) was heated to reflux for 3 hours. After cooling, the mixture was concentrated in vacuo and the residue was dissolved in a mixture of ethyl acetate and water and basified with 2M aqueous sodium hydroxide solution. The layers were separated and the aqueous layer was extracted several times with ethyl acetate. The combined organic layers were dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 50-100% and then a mixture of methanol and ethyl acetate (5%) to give methyl 7-amino-4H-5-oxa-3,9b-diazacyclopenta[a]naphthalene-6-carboxylate (0.383 g) as a sandy coloured solid.