4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン

4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン 化学構造式
730-68-7
CAS番号.
730-68-7
化学名:
4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン
别名:
4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン;メチオツリアート;メチツラールナトリウム;5-[2-(メチルスルファニル)エチル]-5-(ペンタン-2-イル)-2-(ソジオスルファニル)-1,4,5,6-テトラヒドロピリミジン-4,6-ジオン
英語名:
methitural sodium
英語别名:
Neraval;Sch 3132;Methioturiate;Einecs 211-985-3;methitural sodium;Methitural sodium salt;5-(1-Methylbutyl)-5-(2-(methylthio)ethyl)-2-thiobarbituric acid sodium salt;Barbituric acid, 5-(1-methylbutyl)-5-(2-(methylthio)ethyl)-2-thio-, sodium salt;sodium,5-(2-methylsulfanylethyl)-5-pentan-2-yl-2-sulfanylidenepyrimidin-3-ide-4,6-dione;4,6-Dihydro-5-(1-methylbutyl)-5-[2-(methylthio)ethyl]-2-sodiothio-4,6(1H,5H)-pyrimidinedione
CBNumber:
CB4891019
化学式:
C12H21N2NaO2S2
分子量:
312.42
MOL File:
730-68-7.mol

4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン 物理性質

安全性情報

4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン 化学特性,用途語,生産方法

Originator

Neraval ,Schering,US,1956

Manufacturing Process

A solution of 69 g of sodium in 1,380 cc of absolute alcohol is mixed with 257.4 g of β-methylthioethyl-(1-methyl)-n-butyl-cyano-acetic acid ethyl ester and 114 g of thiourea and the whole mass boiled under reflux with stirring for six hours. After concentration under vacuum the residue is taken up in 1.5 liters of water and shaken up thrice, each time with 300 cc of ether. The aqueous alcoholic layer is stripped, under vacuum, of the dissolved ether and mixed with 300 cc of 30% acetic acid under stirring and ice cooling. The precipitated material is sucked off, washed with water, dried and recrystallized from isopropyl alcohol. The thus obtained β-methyl-thioethyl-(1-methyl)-nbutyl-cyano-acetyl thiourea forms yellowish green crystals having a melting point of 229°C to 230C.
100 g of this product are boiled under reflux for three hours with 1 liter of 20% sulfuric acid. After cooling the mixture is taken up in ether, the ether solution washed with water, dried, filtered, concentrated and drawn off under vacuum. The residue is caused to crystallize by treatment with a mixture of 60 volume parts of methanol and 40 volume parts of petroleum benzene. The isolated crystals are recrystallized from the mentioned solvent mixture and yield thereby 5-β-methyl-thioethyl-5-(1-methyl)-n-butyl-2-thiobarbituric acid having a melting point of 79°C to 81°C.
20 g of the free acid are shaken up (in a machine) for one hour with 69.5 cc n/l (normal) caustic soda. The filtered solution is concentrated under vacuum, the residue is taken up in absolute alcohol and again with drawn under vacuum. After two recrystallizations of the residue from isopropyl alcohol one obtains the readily water-soluble, analytically pure, sodium salt of the 5-βmethyl-thioethyl-5-(1 -methyl)-n-butyl-2-thiobarbituric acid.

Therapeutic Function

Hypnotic, Sedative

4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン 上流と下流の製品情報

原材料

準備製品


4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン 生産企業

Global( 1)Suppliers
名前 電話番号 電子メール 国籍 製品カタログ 優位度
Lanospharma Laboratories Co.,Ltd --
sales@lanospharma.com China 6329 56

  • 730-68-7
  • methitural sodium
  • 4,6-Dihydro-5-(1-methylbutyl)-5-[2-(methylthio)ethyl]-2-sodiothio-4,6(1H,5H)-pyrimidinedione
  • Methioturiate
  • 5-(1-Methylbutyl)-5-(2-(methylthio)ethyl)-2-thiobarbituric acid sodium salt
  • Barbituric acid, 5-(1-methylbutyl)-5-(2-(methylthio)ethyl)-2-thio-, sodium salt
  • Einecs 211-985-3
  • Methitural sodium salt
  • Neraval
  • Sch 3132
  • sodium,5-(2-methylsulfanylethyl)-5-pentan-2-yl-2-sulfanylidenepyrimidin-3-ide-4,6-dione
  • 4,6-ジヒドロ-5-(1-メチルブチル)-5-[2-(メチルチオ)エチル]-2-ソジオチオ-4,6(1H,5H)-ピリミジンジオン
  • メチオツリアート
  • メチツラールナトリウム
  • 5-[2-(メチルスルファニル)エチル]-5-(ペンタン-2-イル)-2-(ソジオスルファニル)-1,4,5,6-テトラヒドロピリミジン-4,6-ジオン
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