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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1674822생성일: 2026년 10월 26일

Quinoxaline-6-carboxaldehyde → 6-[[4-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]quinoxaline

https://huagongshe.com/reaction/1674822

반응식

참여 물질

역할이름HCID투입량
반응물Quinoxaline-6-carboxaldehydeHCID 763958—
반응물6-Piperazino-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 1476862—
생성물6-[[4-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]quinoxalineHCID 67339640—

반응 단계

Reductive amination of 6-(piperazin-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine with quinoxaline-6-carbaldehyde was carried out according to General Synthetic Method 5. The crude product was purified by hplc using a Waters XBridge Prep C18 OBD column (5μ silica, 19 mm diameter, 100 mm length) eluted with decreasingly polar mixtures of water (containing 1% aqueous ammonia) and acetonitrile as eluents to give 6-[[4-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]quinoxaline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003649B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-44c1501794454ca69c96faad7bba30ce
출처 메모uspto-grants-2011_08