2-Propanol, reaction products with ammonia, distn. residues → 7-Bromothieno[3,2-d]pyrimidin-2-amine
Reaktionsgleichung
[Br:1][C:2]1[C:6]2[N:7]=[C:8](Cl)[N:9]=[CH:10][C:5]=2[S:4][CH:3]=1.C(O)(C)C.[NH3:16]>>[Br:1][C:2]1[C:6]2[N:7]=[C:8]([NH2:16])[N:9]=[CH:10][C:5]=2[S:4][CH:3]=1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
7-Bromo-2-chlorothieno[3,2-d]pyrimidine (1.0 g, 4.03 mmol) was dissolved in 2.0 M ammonia isopropanol (10 mL) and stirred at 100° C. for 48 hours in a sealed reactor. The reaction mixture was cooled to room temperature and then concentrated. Purification by chromatography (50% ethyl acetate/hexane) yielded a brown solid compound (560 mg, 60% yield).
Aufarbeitung
- temperatureThe reaction mixture was cooled to room temperature
- concentrationconcentrated
- customPurification by chromatography (50% ethyl acetate/hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-9862b7860b4f439c99102ef99dba6a4b
- Quelldatensatz
- uspto-grants-2013_11
- Patentnummer
- US08586580B2
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