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HRID 596368作成日:2026年10月24日

Potassium Iodide → HCID 21437288、化合物

https://huagongshe.com/ja/reaction/596368

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium HydroxideHCID 14797—
反応物(Cyclopropylmethyl)ammonium chlorideHCID 81671—
反応物8-(trifluoromethyl)-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 21330780—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 21437288HCID 21437288—

反応手順

A stirred solution of potassium hydroxide (3.37 g., 0.06 mole) in methanol (30 ml.) is cooled in an ice bath, under nitrogen, and treated with (cyclopropylmethyl)-amine hydrochloride (6.45 g., 0.06 mole). The resulting mixture is kept in the ice bath for 15 minutes, treated with tetrahydrofuran (250 ml.), 8-(trifluoromethyl)-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine (6.86 g., 0.02 mole) and potassium iodide (3.32 g., 0.02 mole) and kept at ambient temperature for 18 hours. The mixture is concentrated and the residue is mixed with water and extracted with methylene chloride. The extract is washed with brine, dried over anhydrous sodium sulfate and concentrated. The product is crystallized once from ethyl acetate and once from methylene chloride ethyl acetate to give 8-(trifluoromethyl)-1-[[(cyclopropylmethyl)amino]methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine. Preparation 28 8 -Chloro-1-[[(cyclopropylmethyl)amino] methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04010177
出典データセットuspto-grants-1977_03
ORD IDord-b85af1f64e684f52a0aff5d18ad57932
出典メモuspto-grants-1977_03