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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329220생성일: 2026년 10월 25일

alpha-Hydroxytriazolam → 4-[alpha-Amino-4-chloro-alpha-(o-chlorophenyl)-o-tolyl]-3-hydroxymethyl-5-methyl-4H-1,2,4-triazole

https://huagongshe.com/reaction/329220

반응식

참여 물질

역할이름HCID투입량
반응물alpha-HydroxytriazolamHCID 1963—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물4-[alpha-amino-4-chloro-alpha(o-chlorophenyl)-o-tolyl]-3-cyclopropyl-5-methyl-4H-1,2,4-triazoleHCID 86733716—
용매Diethylene GlycolHCID 8117—
생성물4-[alpha-Amino-4-chloro-alpha-(o-chlorophenyl)-o-tolyl]-3-hydroxymethyl-5-methyl-4H-1,2,4-triazoleHCID 86733717—

반응 단계

A mixture of 10.776 g. 8-chloro-6-(o-chlorophenyl)-1-hydroxymethyl-4H-s-triazolo[4,3-a] [1,4]benzodiazepine (111) (30.0 mmoles) and 7.50 ml. of hydrazine hydrate in 60 ml. of diethylene glycol is heated to 150°-160° C. for about 18 hours. The reaction is then quenched in a cold aqueous 5% sodium hydroxide solution and the product extracted with chloroform. The extracts thus obtained are dried over anhydrous magnesium sulfate and concentrated in vacuo to give 13.0 g. of oil which is crystallized from methanol/ethyl acetate to give 1.93 g. of a mixture of the A and B isomers (ratio 81/19) of 4-[α-amino-4-chloro-α-(o-chlorophenyl)-o-tolyl]-3-(hydroxymethyl)-5-methyl-4H-1,2,4-triazole (I) m.p. 205°-215° C. The mixture thus obtained is recrystallized from the same solvent mixture to give 0.76 g. of 4-[α-amino-4-chloro-α-(o-chlorophenyl)-o-tolyl]-o-tolyl]-3-(hydroxymethyl)-5-methyl-4H-1,2,4-triazole (I), (isomer A) melting at 218° - 223° C., and having infrared (mull) spectral absorptions at 3330, 3240, 3150, 3060, 2680, 1600, 1570, 1530, 1515 and 1485 cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04020085
출처 데이터셋uspto-grants-1977_04
ORD IDord-0dc91a445a504286ac33cca0d4205d3a
출처 메모uspto-grants-1977_04