Reaktionsgleichung
[Br:1][C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[C:9]([NH:12][C:13]1[CH:17]=[CH:16][S:15][C:14]=1[C:18](O)=[O:19])(=O)[CH3:10].P(Cl)(Cl)Cl>N1C=CC=CC=1>[CH3:10][C:9]1[N:4]([C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=2[Br:1])[C:18](=[O:19])[C:14]2[S:15][CH:16]=[CH:17][C:13]=2[N:12]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 105 °C
Versuchsvorschrift
To a mixture of pyridine (6 mL), 2-bromoaniline (1.03 g, 6 mmol), and 3-acetamidothiophene-2-carboxylic acid (0.555 g, 3 mmol) was added phosphorus trichloride (0.03 mL, 3.45 mmol). The reaction was heated to 105° C. for 4 hours, cooled to ambient temperature and partitioned between chloroform and water (an insoluble precipitate was removed by filtration). Phases were separated and the aqueous layer was extracted with chloroform. The combined organic phase was washed with water and brine, dried over magnesium sulfate and concentrated to a dull yellow film. This residue was flash chromatographed on silica gel (30×125 mm) eluting with 15-25% ethyl acetate/hexane to afford 0.411 g (47%) of 2-methyl-3-(2-bromophenyl)-3H-thieno[3,2-d]pyrimidin-4-one as a yellow foam.
Aufarbeitung
- temperaturecooled to ambient temperature
- custompartitioned between chloroform and water (an insoluble precipitate
- customwas removed by filtration)
- customPhases were separated
- extractionthe aqueous layer was extracted with chloroform
- washThe combined organic phase was washed with water and brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated to a dull yellow film
- customchromatographed on silica gel (30×125 mm)
- washeluting with 15-25% ethyl acetate/hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-8b0145d477cd4b0a9aa4447538ad2cc6
- Quelldatensatz
- uspto-grants-1999_10
- Patentnummer
- US05962457
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