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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 596351생성일: 2026년 10월 25일

2-Hydroxyacetohydrazide → alpha-Hydroxytriazolam

https://huagongshe.com/reaction/596351

반응식

참여 물질

역할이름HCID투입량
반응물2-HydroxyacetohydrazideHCID 350536—
반응물7-chloro 5-(2-chlorophenyl)-1,3-dihydro-2H-(1,4)-benzodiazepine-2-thioneHCID 826703—
용매1-ButanolHCID 263—
생성물alpha-HydroxytriazolamHCID 1963—

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04010177
출처 데이터셋uspto-grants-1977_03
ORD IDord-110925dc63aa4b38be6253d683625cd7
출처 메모uspto-grants-1977_03