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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 464288생성일: 2026년 10월 24일

Diethylamine → N,N-diethyl-1-methyl-[1,2,4]triazolo[4,3-a]quinoxalin-4-amine

https://huagongshe.com/ko/reaction/464288

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물DipropylamineHCID 8902—
반응물4-Chloro[1,2,4]triazolo[4,3-a]quinoxalineHCID 1126118—
반응물4-Chloro-1-methyl[1,2,4]triazolo[4,3-a]quinoxalineHCID 2768643—
생성물N,N-diethyl-1-methyl-[1,2,4]triazolo[4,3-a]quinoxalin-4-amineHCID 89950454%

반응 단계

This compound was prepared by the method of Example 11, utilizing 4-chloro-1-methyl-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 3) as starting material in place of 4-chloro-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 2) and diethylamine as reagent in place of di-n-propylamine. The crude product obtained was recrystallized from chloroform and then from cyclohexane to afford 7.2 g. (54% yield) of pure 4-diethylamino-1-methyl-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 123°-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04547501
출처 데이터셋uspto-grants-1985_10
ORD IDord-60902d7a6a584149b5bad04a7a52c7f5
출처 메모uspto-grants-1985_10