メチル硫酸ヘキソシクリウム

メチル硫酸ヘキソシクリウム 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

メチル硫酸ヘキソシクリウム 化学特性,用途語,生産方法

効能

鎮痙薬, ムスカリン受容体拮抗薬

Originator

Tral,Abbott,US,1957

使用

Hexocyclium inhibits muscarinic action of acetylcholine on postganglionic parasympathetic effector regions. It is used for treating stomach ulcers.

Manufacturing Process

In a 2-liter, 3-necked, round-bottomed flask equipped with a stirrer, dropping funnel, and a condenser protected with a calcium chloride drying tube is placed 13.7 grams (0.57 mol) of magnesium turnings and the magnesium is covered with 200 cc of anhydrous ether. A crystal of iodine is added to the flask and 92.9 grams (0.57 mol) of cyclohexyl bromide dissolved in 300 cc of anhydrous ether is added dropwise with stirring while the reaction proceeds. After the addition of the cyclohexyl bromide is completed, the resulting mixture is stirred and heated on a steam bath for 3 hours. The mixture is cooled to room temperature and 49.5 grams (0.227 mol) of N-phenacyl-N'- methylpiperazine dissolved in 50 cc of anhydrous ether is added dropwise and the resulting mixture is stirred and re fluxed for about 16 hours.
The reaction mixture is cooled and 50 grams of ammonium chloride dissolved in 200 cc of water is added dropwise thereto with stirring. The decomposed Grignard complex is then filtered. Benzene is added to the ether filtrate and the solvents are removed therefrom on a steam bath. The residue is fractionated and the base, N-(β-cyclohexyl-β-hydroxy-β-phenyl-ethyl)N'- methylpiperazine, is obtained as a liquid having a boiling point of 196° to 203°C at a pressure of 4.0 mm.
To 3.8 grams of the base dissolved in 35 cc of ethyl alcohol is added 1.6 grams of dimethyl sulfate. The solution is allowed to stand at room temperature for about 12 hours. The salt formed is filtered, recrystallized from ethyl alcohol, and is found to have a melting point of 203° to 204°C.

Therapeutic Function

Spasmolytic

合成

Hexocyclium, 4-(|?-cyclohexyl-|?-hydroxyphenethyl)-1,1-piperazinium methylsulfate (14.1.28), is synthesized by alkylating 1-methylpiperazine with |á-bromacetophenone, which forms 4-methyl-1-phenacylpiperazine (14.1.26). Reacting this with cyclohexylmagnesiumbromide gives 4-(|?-cyclohexyl-|?-hydroxyphenethyl)-1,1-piperazine (14.1.27), the alkylation of which using dimethylsulfate gives hexocyclium [23].

メチル硫酸ヘキソシクリウム 上流と下流の製品情報

原材料

準備製品

メチル硫酸ヘキソシクリウム 生産企業

名前	電話番号	電子メール	国籍	製品カタログ	優位度
TargetMol Chemicals Inc.	+1-781-999-5354 +1-00000000000	marketing@targetmol.com	United States	19892	58
Hangzhou MolCore BioPharmatech Co.,Ltd.	+86-057181025280; +8617767106207	sales@molcore.com	China	49739	58
TargetMol Chemicals Inc.	4008200310	marketing@tsbiochem.com	China	24017	58

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• 115-63-9
• Nsc30256
• Piperazinium, 4-(.beta.-cyclohexyl-.beta.-hydroxyphenethyl)-1,1-dimethyl-, methyl sulfate
• Piperazinium, 4-(2-cyclohexyl-2-hydroxy-2-phenylethyl)-1,1-dimethyl-, methyl sulfate (salt)
• hexocyclium metilsulfate
• Hexocyclium
• Hexocyclium methosulfate
• 4-(.beta.-Cyclohexyl-.beta.-hydroxyphenethyl)-1,1-dimethylpiperazinium methyl sulfate
• Ab 803
• Hexacyclium methyl sulfate
• Hexocyclium methyl sulfate
• 4-(2-Cyclohexyl-2-hydroxy-2-phenylethyl)-1,1-dimethylpiperazin-1-ium Methyl Sulfate
• Traline
• メチル硫酸ヘキソシクリウム
• 4-(2-シクロヘキシル-2-ヒドロキシ-2-フェニルエチル)-1,1-ジメチルピペラジニウム・メチルスルファート
• 1,1-ジメチル-4-(2-フェニル-2-シクロヘキシル-2-ヒドロキシエチル)ピペラジン-1-イウム・メチルスルファート