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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1674902생성일: 2026년 10월 25일

N-(3-formylphenyl)acetamide → N-[3-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]phenyl]acetamide

https://huagongshe.com/reaction/1674902

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-formylphenyl)acetamideHCID 256849—
반응물6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
생성물N-[3-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]phenyl]acetamideHCID 67340176—

반응 단계

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with N-(3-formylphenyl)acetamide was carried out according to General Synthetic Method 7. The crude product was purified by hplc using a Waters XBridge Prep C18 OBD column, 5μ silica, 30 mm diameter, 100 mm length eluted with decreasingly polar mixtures of water (containing 0.1% aqueous ammonia) and acetonitrile as eluents to give N-[3-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]phenyl]acetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003649B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-8497f34117544dc9b025e5eaffb72f7b
출처 메모uspto-grants-2011_08