HCID 14372129, Verbindung → HCID 14372146, Verbindung
Reaktionsgleichung
[S:1]([C:5]1[O:13][C:12]2[CH:11]=[CH:10][N:9]=[C:8]([O:14]C)[C:7]=2[CH:6]=1)(=[O:4])(=[O:3])[NH2:2]>Cl>[S:1]([C:5]1[O:13][C:12]2[CH:11]=[CH:10][NH:9][C:8](=[O:14])[C:7]=2[CH:6]=1)(=[O:3])(=[O:4])[NH2:2]Komponenten
3
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
Alternate Procedure: A suspension of 2-sulfamoyl-4-methoxyfuro[3,2-c]pyridine (0.75 g, 3.3 mmol) in 10% aqueous hydrochloric acid (40 ml) was heated at 100° C. for 41/2 hours. Upon cooling, the product precipitated and was collected by filtration, washed with ethanol and diethyl ether to give 0.53 g (76% yield), m.p. 286°-289° C.
Aufarbeitung
- temperatureUpon cooling
- customthe product precipitated
- filtrationwas collected by filtration
- washwashed with ethanol and diethyl ether
- customto give 0.53 g (76% yield), m.p. 286°-289° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-15a743b8f9f34950ab9a807d78b7956e
- Quelldatensatz
- uspto-grants-1989_02
- Patentnummer
- US04808595
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