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HRID 596351作成日:2026年10月24日

2-Hydroxyacetohydrazide → alpha-Hydroxytriazolam

https://huagongshe.com/ja/reaction/596351

反応式

関与物質

役割名称HCID仕込み量
反応物2-HydroxyacetohydrazideHCID 350536—
反応物7-chloro 5-(2-chlorophenyl)-1,3-dihydro-2H-(1,4)-benzodiazepine-2-thioneHCID 826703—
溶媒1-ButanolHCID 263—
生成物alpha-HydroxytriazolamHCID 1963—

反応手順

A solution of 1,3-dihydro-7-chloro-5-(o-chlorophenyl)-2H-1,4-benzodiazepine-2-thione (9.63 g., 0.03 mole) and hydroxy-acetic acid hydrazide (6.66 g.) in n-butyl alcohol (300 ml.) is refluxed for about 15 hours with a slow stream of nitrogen bubbling through the reaction mixture for the first hour. The mixture is then cooled and concentrated in vacuo and the resulting residue is suspended in water, treated with a little ether and crystallized. The solid is collected by filtration and dried in vacuo. Recrystallization of this material from methylene chloride-methanol gives 8-chloro-1-(hydroxymethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine in three crops: 4.96 g. of melting point 239°-241° C., 1.58 g. of melting point 236°-239° C., and 0.365 g. of melting point 232°-236° C. The analytical sample has a melting point of 239.5°-241° C. Anal. calcd. for C17H12Cl2N4O: C, 56.84; H, 3.37; Cl, 19.74; N, 15.60. Found: C, 56.27; H, 3.28; Cl, 19.75; N, 15.55. Preparation 2 8-Chloro-1-(hydroxymethyl)-6-phenyl-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-110925dc63aa4b38be6253d683625cd7
出典メモuspto-grants-1977_03