(R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(cyclopentyl)amino)butanoate → HCID 24739252、化合物

関与物質

反応条件

反応手順

Methyl (2R)-2-[(2-chloro-5-nitro-pyrimidin-4-yl)-cyclopentyl-amino]butanoate 1m (1 g, 3 mmol) was dissolved in 10 mL of acetic acid followed by the addition of Raney nickel (0.50 g), filled with hydrogen three times, then heated to 75-80° C. and stirred for 12 hours. The reaction mixture was filtered, washed with dichloromethane (50 mL). The filtrate was concentrated under reduced pressure, added with 100 mL ethyl acetate, washed with water (50 mL×3) and saturated sodium chloride solution (50 mL×3) successively. The combined organic phase was dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound (7R)-2-chloro-8-cyclopentyl-7-ethyl-7,8-dihydro-5H-pteridin-6-one 1n (0.56 g, yield: 66.7%) as a white solid.

情報源と証拠