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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38821생성일: 2026년 10월 23일

Diisopropylethylamine → 6-Bromo-N'-(4-morpholinylacetyl)-1H-indazole-4-carbohydrazide

https://huagongshe.com/ko/reaction/38821

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Morpholineacetic acidHCID 438968—
반응물6-bromo-1H-indazole-4-carbohydrazideHCID 66692002—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물6-Bromo-N'-(4-morpholinylacetyl)-1H-indazole-4-carbohydrazideHCID 66691612103%

반응 조건

온도20 °C

반응 단계

O-(7-Azabenzotriazol-1-yl)-N,N,N′N′-tetramethyluronium hexafluorophosphate (0.841 g, 2.212 mmol) was dissolved in N,N-dimethylformamide (5 ml) then treated with 4-morpholinylacetic acid (0.304 g, 2.092 mmol) and then N,N-diisopropyethylamine (0.386 ml, 2.212 mmol). The clear solution was stirred at 20° C. for 10 mins then to this was added 6-bromo-1H-indazole-4-carbohydrazide (0.513 g, 2.011 mmol) as a partial solution in N,N-dimethylformamide (8 ml). The clear solution was stirred at 20° C. for 72 h under nitrogen. It was then reduced in volume to ˜1 ml, diluted with methanol (5 ml) and loaded onto an aminopropyl cartridge which had been pre-conditioned with methanol. The fully-loaded cartridge was left to stand for 2 h then eluted with methanol and the eluant evaporated to give an orange oil. This was diluted with dichloromethane (3 ml) and loaded onto a silica (10 g) cartridge. This was eluted with a gradient of methanol and ethyl acetate to give the title compound as a beige solid (0.792 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524751B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-78a8616a601f478ab82f913da2b5f487
출처 메모uspto-grants-2013_09