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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657875생성일: 2026년 10월 26일

1-Butyl-3-methylimidazolium hexafluorophosphate → N*6*,N*6*-Diethyl-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazine-3,6-diamine

https://huagongshe.com/reaction/657875

반응식

참여 물질

역할이름HCID투입량
반응물1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
반응물6-Chloro-7,8-dimethyl-[1,2,4]triazolo[4,3-B]pyridazin-3-amineHCID 58045804—
용매DiethylamineHCID 8021—
생성물N*6*,N*6*-Diethyl-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazine-3,6-diamineHCID 58045894—

반응 단계

6-Chloro-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine (W2.006a, 800 mg and 650 mg divided between 2 microwave vessels) was initially charged each dissolved in 12 ml of diethylamine and admixed with 1-butyl-3-methylimidazolium hexafluorophosphate (150 μl). Subsequently, they were placed into the microwave at 180° C. for 4 h. In order to complete the reaction, they were placed again into the microwave at 180° C. for 4 h and then left to stand overnight. The two reaction mixtures were combined in a round-bottom flask and dried. The residue was admixed with water and extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was purified by means of preparative HPLC (met. F), and the clean product fractions were combined, freed of the acetonitrile under reduced pressure, alkalized with saturated potassium carbonate solution and extracted repeatedly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated. 900 mg of the title compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076336B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-cf89ee8961294bbca38c75059dd07309
출처 메모uspto-grants-2011_12