Acetic Acid → 5,7-Dihydrothieno[3,4-d]pyrimidine-2,4-diol
Reaktionsgleichung
C(S[C:4]1[NH:5][C:6](=[O:13])[C:7]2[CH2:12][S:11][CH2:10][C:8]=2[N:9]=1)C.Cl.CC(O)=[O:17]>O>[NH:9]1[C:8]2[CH2:10][S:11][CH2:12][C:7]=2[C:6](=[O:13])[NH:5][C:4]1=[O:17]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To the suspension of 2-(ethylthio)thieno[3,4-d]pyrimidin-4-(3H, 5H, 7H)-one (2.88 g, 13.45 mmol) in water (20 mL) was added 2.0 mL of cone. HCl and 4.0 mL of AcOH. The reaction was heated at reflux overnight then cooled and the solid collected by filtration, washed with water and methanol, evaporated and dried to obtain a white solid thieno[3,4-d]pyrimidine-2,4-(1H, 3H, 5H, 7H)-dione (1.80 g, 80%). Without further purification, the crude product was used directly in the next step.
Aufarbeitung
- additionwas added 2.0 mL of cone
- temperatureThe reaction was heated
- temperatureat reflux overnight
- temperaturethen cooled
- filtrationthe solid collected by filtration
- washwashed with water and methanol
- customevaporated
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-e4e56741e6b54b6a9f8cb47a7dfc6b7f
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09242993B2
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