Allylamine → HCID 15908146, Verbindung

Reaktionsgleichung

Cl[C:2]1[N:3]=[C:4]([NH:14][CH3:15])[C:5]2[S:10][CH:9]=[C:8]([CH:11]([CH3:13])[CH3:12])[C:6]=2[N:7]=1.[CH2:16]([NH2:19])[CH:17]=[CH2:18].C(=O)([O-])O.[Na+]>>[CH2:16]([NH:19][C:2]1[N:3]=[C:4]([NH:14][CH3:15])[C:5]2[S:10][CH:9]=[C:8]([CH:11]([CH3:13])[CH3:12])[C:6]=2[N:7]=1)[CH:17]=[CH2:18]

Komponenten

Edukt 3

HCID 7853Allylamine

HCID 516892Sodium Bicarbonate

HCID 15908145HCID 15908145, Verbindung

Produkt 1

HCID 15908146HCID 15908146, VerbindungAusbeute 91,7 %

Versuchsvorschrift

90 mg (0.37 mmol) of 2-chloro-7-isopropyl-4-methylaminothieno[3,2-d]pyrimidine and 340 mg (5.96 mmol) of allylamine were heated in a sealed tube at 160° C. for 16 hours. After completion of the reaction, the reaction mixture was allowed to resume room temperature, followed by adding a saturated aqueous sodium hydrogen carbonate solution thereto and extraction with ethyl acetate (50 ml×2). After the organic layer was washed with brine and dried over anhydrous sodium sulfate, the solvent was distilled off. The residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1/4) to give 89 mg (yield: 91.1%) of the title compound.