Hydrochloric Acid → methyl 6-bromo-1H-indazole-4-carboxylate
Reaktionsgleichung
Cl.[Br:2][C:3]1[CH:4]=[C:5]([C:12]([OH:14])=[O:13])[C:6]2[CH:7]=[N:8][NH:9][C:10]=2[CH:11]=1.[CH3:15]O>>[Br:2][C:3]1[CH:4]=[C:5]([C:12]([O:14][CH3:15])=[O:13])[C:6]2[CH:7]=[N:8][NH:9][C:10]=2[CH:11]=1Komponenten
4
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
Concentrated hydrochloric acid (46.9 ml, 1543 mmol) was added to a stirred suspension of 6-bromo-1H-indazole-4-carboxylic acid (4.65 g, 19.29 mmol, available from Sinova) in methanol (100 ml) and the reaction mixture was heated to 70° C. for 18 h. The reaction mixture was allowed to cool to RT resulting in the precipitation of a solid. The mixture was cooled in ice and the yellow precipitate filtered off and washed with methanol to give the title compound as a yellow solid (2.54 g).
Aufarbeitung
- temperatureto cool to RT
- customresulting in the precipitation of a solid
- temperatureThe mixture was cooled in ice
- filtrationthe yellow precipitate filtered off
- washwashed with methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-bb1057ad54f042b3ad221420156e2f68
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09326987B2
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