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HRID 279943作成日:2026年10月27日

Isopropanol → N-methyl-S-methyl-N'-[2-(2-dimethylaminomethylthiazol-4-ylmethylthio)ethyl]isothiourea

https://huagongshe.com/reaction/279943

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Methanesulfonic AcidHCID 6395—
反応物N-Methyl-dithiocarbonimidic acid dimethyl esterHCID 140427—
反応物2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazoleHCID 10977318—
溶媒WaterHCID 962—
生成物N-methyl-S-methyl-N'-[2-(2-dimethylaminomethylthiazol-4-ylmethylthio)ethyl]isothioureaHCID 178484985—

反応手順

Ten g. of 2-dimethylaminomethyl-4-(2-aminoethyl)thiomethylthiazole was dissolved in 100 ml. of isopropanol, and 2.8 ml. of methanesulfonic acid was added, followed by 6.5 g. of methylcarbonimidodithioic acid, dimethyl ester. The mixture was stirred under reflux for 16 hours, and was evaporated under vacuum to obtain a residue, which was taken up in 100 ml. of water. The solution was extracted with two 25 ml. portions of dichloromethane, and the aqueous layer was cooled. Fifty ml. of dichloromethane and 15 ml. of 50% aqueous sodium hydroxide were added. The layers were separated, and the solution was extracted again with 50 ml. of dichloromethane. The organic layers were combined, dried over potassium carbonate and evaporated under vacuum to obtain 10.3 g. of product, substantially identical to that of Example 1, which was 96.7% pure by HPLC analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04587344
出典データセットuspto-grants-1986_05
ORD IDord-9f074c3ff4f94a24bfc6dcc9f5024de8
出典メモuspto-grants-1986_05