Dimethylformamide → (3-Propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene)methylamine
反応式
[CH2:1]([N:4]1[C:9](=N)[C:8]2[CH:11]=[CH:12][S:13][C:7]=2[N:6]=[C:5]1[O:14][CH2:15][CH2:16][CH3:17])[CH2:2][CH3:3].CI.C(=O)([O-])[O-].[K+].[K+].[CH3:26][N:27](C=O)C>>[CH2:1]([N:4]1[C:9](=[CH:26][NH2:27])[C:8]2[CH:11]=[CH:12][S:13][C:7]=2[N:6]=[C:5]1[O:14][CH2:15][CH2:16][CH3:17])[CH2:2][CH3:3]参加物
5
実験手順
In a sulfonation flask 4.5 g (0.018 mol) 3-propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene amine, 5.1 g (0.036 mol) CH3I, 5.0 g (0.036 mol) powdered potassium carbonate and 80 ml of absolute DMF are stirred for 4 hours at an internal temperature of 90-100° C. Then the solvent is distilled off in vacuum, the residue taken up in ethylacetate and the organic phase twice washed with water. After drying the organic phase over Na2SO4 the ethylacetate is distilled off in a water jet vacuum and the residue purified by column chromatography over silica gel (eluant: hexane/ethylacetate 1:6). Yield: 4.4 g of (3-propyl-2-propoxy-3H-thieno[2,3-d]pyrimidine-4-ylidene)methylamine in the form of a brown oil.