Pyridine → N1-[4-(4-amino-7-tetrahydro-2H-4-pyranyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-2-methoxyphenyl]benzamide

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Reaktionsschritte

5-(4-Amino-3-methoxyphenyl)-7-tetrahydro-2H-4-pyranyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (80 mg, 0.236 mmol) was dissolved in dichloromethane (2.0 mL). Pyridine (2.0 mL) was added followed by benzoyl chloride (41 uL, 0.353 mmol). After stirring at room temperature for 2 hours, the solvent was removed and the residue was dissolved in 1 ml DMSO, methanol (1 mL) was added and precipitate was formed. The solid was collected by filtration to give N1-[4-(4-amino-7-tetrahydro-2H-4-pyranyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-2-methoxyphenyl]benzamide (64 mg, 0.144 mmol). 1H NMR (CDCl3-d) δ 2.12(m, 4H), 3.67(m, 2H), 3.99(s, 3H), 4.17(m, 2H), 4.99(m, 1H), 7.03(s, 1H), 7.04(s, 1H), 7.14(d, J=8.2 Hz, 1H), 7.53(m, 3H), 7.94(d, J=7.8 Hz, 1H), 8.33(s, 1H), 8.58(s, 1H), 8.63(d, J=8.2 Hz, 1H). LC/MS: MH+=444.

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