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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 918263생성일: 2026년 10월 24일

Hydrazine hydrate (1:1) → 4-[alpha-Amino-4-chloro-alpha-(o-chlorophenyl)-o-tolyl]-3-[(dimethylamino)methyl]-5-methyl-4h-1,2,4-triazole

https://huagongshe.com/ko/reaction/918263

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물8-chloro-6-(o-chlorophenyl)-1-cyclopropyl-4H-s-triazolo[4,3-a][1,4] benzodiazepineHCID 86733715—
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-[(dimethylamino)methyl]-5-methyl-4h-1,2,4-triazoleHCID 86733714—

반응 단계

A solution of 7.38 g. of 8-chloro-6-(o-chlorophenyl)-1-(dimethylamino)methyl-4H-s-triazolo[4,3 -a][1,4] benzodiazepine (III) (20.0 mmol.) and 5.0 ml. of hydrazine hydrate in 50 ml. of diethylene glycol is heated to about 140° C. for about 18 hours. The reaction is quenched in a cold aqueous 5% sodium hydroxide solution, and the product extracted with chloroform. The extracts are dried and concentrated in vacuo to yield 8.5 g. of oil, which is crystallized from ethyl acetate/hexane mixtures to give 4.0 g. of 4-[α-amino-4-chloro-α-(o-chlorophenyl)-o-tolyl]-3-[(dimethylamino)methyl]-5-methyl-4H-1,2,4 -triazole (I), isomer A, m.p. 142°-144° C., an analytical sample of which melts at 148°-150° C. and has infrared (mull) spectral absorptions at 3380, 3270, 3200, 3070, 2770, 1610, 1590, 1570, 1530 and 1520 cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03970666
출처 데이터셋uspto-grants-1976_07
ORD IDord-dce2467bfab9484b836a4426c9b1c792
출처 메모uspto-grants-1976_07