3-Amino-1-propanol → Dipyridodiazepinone deriv. 24

HRID 53550

Reaktionsgleichung

Reaktionsgleichung von HRID 53550
Cl[C:2]1[CH:3]=[C:4]([CH3:20])[C:5]2[NH:6][C:7](=[O:19])[C:8]3[CH:18]=[CH:17][CH:16]=[N:15][C:9]=3[N:10]([CH2:13][CH3:14])[C:11]=2[N:12]=1.[NH2:21][CH2:22][CH2:23][CH2:24][OH:25]>>[CH2:13]([N:10]1[C:9]2[N:15]=[CH:16][CH:17]=[CH:18][C:8]=2[C:7](=[O:19])[NH:6][C:5]2[C:4]([CH3:20])=[CH:3][C:2]([NH:21][CH2:22][CH2:23][CH2:24][OH:25])=[N:12][C:11]1=2)[CH3:14]

Komponenten

3

Edukt 2

HCID 90863-Amino-1-propanolHCID 463144Dipyridodiazepinone deriv. 15

Produkt 1

HCID 463151Dipyridodiazepinone deriv. 24

Versuchsvorschrift

The title compound, m.p. 222°-224° C., was synthesized from 2-chloro-5,11-dihydro-11-ethyl-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one and 3-aminopropanol using procedures analogous to those described above, except that the mixture was heated in a pressure bottle at 210° C. for 40 min., and the product was crystallized from ethyl acetate.

Quellen und Nachweise

ORD-Eintrag
ord-5844411c24cd4bec8e690adcbf227b5e
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05620974

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