Methane → HCID 178518411, Verbindung
Reaktionsgleichung
ClC1N=[C:4](NC2C=C(C=CC=2)C(O)=O)[C:5]2[S:10][CH2:9][CH2:8][C:6]=2N=1.[NH2:21][C:22]([NH2:24])=[O:23].C.[OH-:26].[Na+]>>[N:21]1[C:6]2[CH:8]=[CH:9][S:10][C:5]=2[C:4]([OH:26])=[N:24][C:22]=1[OH:23]Komponenten
5
Versuchsvorschrift
10.0 g (64.0 mmol) of methylester 3-aminothiophene-2-carboxylate (I) and 19.0 g (31.60 mmol) of urea are mixed and melted for 2 hours at 200° C. After cooling, the reaction mixture is dissolved in 1 molar sodium hydroxide solution and decolorized with activated charcoal. It is filtered and the filtrate is cooled and acidified with 4M hydrochloric acid. The precipitate formed is suction filtered and dried. 8.03 g of product II (75%) is obtained as a powder.
Aufarbeitung
- temperatureAfter cooling
- filtrationIt is filtered
- temperaturethe filtrate is cooled
- customThe precipitate formed
- filtrationfiltered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-af2a06948cb2485f8b3359544a4488d2
- Quelldatensatz
- uspto-grants-2013_01
- Patentnummer
- US08354531B2
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