1,3,4,6,7,11b-ヘキサヒドロ-2H-ピラジノ[2,1-a]イソキノリン

1,3,4,6,7,11b-ヘキサヒドロ-2H-ピラジノ[2,1-a]イソキノリン 価格

1,3,4,6,7,11b-ヘキサヒドロ-2H-ピラジノ[2,1-a]イソキノリン 化学特性,用途語,生産方法

• Originator

  Azaquinzole,Onbio Inc.

• Manufacturing Process

  2 Methods of producing of 1,2,3,6,7,11b-hexahydro-4H-pyrazino-[2,1- a]isoquinoline:
  1). 214.0 g diethyl ester of oxalic acid are mixed with a solution of 238.0 g 1- aminomethyl-1,2,3,4-tetrahydroisoquinoline in 200 ml alcohol are boiled for 7 h. After cooling, the obtained crystals of 1,2,3,6,7,11b-hexahydro-4Hpyrazino[ 2,1-a]isoquinoline-3,4-dione are vacuum-filtered and washed with acetone and dried, melting point 220°C. Yield: 240.0 g.
  55.0 g lithium aluminum hydride are dissolved in 650 ml absolute tetrahydrofuran and mixed dropwise with a suspension of 120.0 g 1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline-3,4-dione in 300 ml absolute tetrahydrofuran. After 7 h of boiling, the residual hydride is decomposed by the addition of water, and the reaction solution is worked up. The obtained 1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline is distilled in vacuum, boiling point 98°-100°C/0.01 mm. Yield: 86.0 g.
  2). 16.2 g 1-aminomethyl-1,2,3,4-tetrahydroisoquinoline and 18.7 g ethylene dibromide are boiled for 4 h in n-butanol, with the addition of 13.8 g potassium carbonate. After the solvent is evaporated, the residue is treated with water, mixed with sodium hydroxide solution, and shaken out with chloroform. The chloroform solution is dried, concentrated by evaporation, and the resulting 1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline is distilled at 98°-100°C/0.01 mm. The yield amounts to 7.5 g.

• Therapeutic Function

  CNS depressant

1,3,4,6,7,11b-ヘキサヒドロ-2H-ピラジノ[2,1-a]イソキノリン 上流と下流の製品情報

1,3,4,6,7,11b-ヘキサヒドロ-2H-ピラジノ[2,1-a]イソキノリン 生産企業

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