2,2',2'',2'''-[(4-ピペリジノピリミド[5,4-d]ピリミジン-2,6-ジイル)ジニトリロ]テトラキスエタノール

2,2',2'',2'''-[(4-ピペリジノピリミド[5,4-d]ピリミジン-2,6-ジイル)ジニトリロ]テトラキスエタノール 化学特性,用途語,生産方法

• Originator

  Rapenton,Thomae,W. Germany,1980

• Manufacturing Process

  3.9 g (0.06 mol) of zinc powder were introduced into a solution of 5.0 g (0.01 mol) of 2,6-bis-(diethanolamino)-4,8-dipiperidino-pyrimido-[5,4-d]-pyrimidine (dipyridamole; see entry under that name for its synthesis) in 120 cc of aqueous 10% formic acid. The resulting mixture was heated on a water bath, while occasionally stirring, until the intense yellow color of the starting compound disappeared, which occurred after about 30 to 40 minutes. Thereafter, the unconsumed zinc powder was separated by vacuum filtration, the virtually colorless filtrate was essentially an aqueous solution of 2,6-bis- (diethanolamino)-8-piperidino-1,2,3,4-tetrahydropyrimido-[5,4-d]pyrimidine.
  The filtrate was adjusted to a pH of 9 by adding concentrated ammonia, and then a 1 N aqueous iodine-potassium iodide solution was added dropwise, whereby the tetrahydropyrimido[5,4-d]pyrimidine obtained by hydrogenation with zinc in formic acid was converted by oxidation into 2,6-bis- (diethanolamino)-8-piperidino-pyrimido-[5,4-d]-pyrimidine. The completion of the oxidation was checked by means of a starch solution. The major amount of the oxidation product already separated out as a deep yellow crystalline precipitate during the addition of the iodine solution. After the oxidation reaction was complete, the reaction mixture was allowed to stand for a short period of time, and then the precipitate was separated by vacuum filtration,washed with water and dried. It had a melting point of 157°C to 158°C. The yield was 8.0 g, which corresponds to 95% theory.

• Therapeutic Function

  Platelet aggregation inhibitor

2,2',2'',2'''-[(4-ピペリジノピリミド[5,4-d]ピリミジン-2,6-ジイル)ジニトリロ]テトラキスエタノール 上流と下流の製品情報

2,2',2'',2'''-[(4-ピペリジノピリミド[5,4-d]ピリミジン-2,6-ジイル)ジニトリロ]テトラキスエタノール 生産企業

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