Thionyl Chloride → 4-Bromothiazole-2-carbohydrazide
Reaktionsgleichung
[Br:1][C:2]1[N:3]=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.O=S(Cl)Cl.O.[NH2:15][NH2:16]>CO>[Br:1][C:2]1[N:3]=[C:4]([C:7]([NH:15][NH2:16])=[O:9])[S:5][CH:6]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of the 4-bromothiazole-2-carboxylic acid (2.0 g, 9.8 mmol) in MeOH (10 mL) was added SOCl2 (710 μL, 9.8 mmol) and the reaction was refluxed for 3 hours. The reaction was concentrated, the residue was suspended in EtOH (10 mL), hydrazine hydrate (2.4 mL, 49 mmol) was added and the reaction was heated to reflux for 90 minutes. The reaction was concentrated, suspended in CH3CN, filtered, and the solids were washed with CH3CN, Et2O, and dried to afford of 4-bromothiazole-2-carbohydrazide as a yellow solid. M+1=222.1
Aufarbeitung
- temperaturethe reaction was refluxed for 3 hours
- concentrationThe reaction was concentrated
- temperaturethe reaction was heated
- temperatureto reflux for 90 minutes
- concentrationThe reaction was concentrated
- filtrationfiltered
- washthe solids were washed with CH3CN, Et2O
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-7a1e2be7825a4e7aab52039a1b0115c1
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09169243B2
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