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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-Butyl-3-methylimidazolium hexafluorophosphate | HCID 2734174 | — |
| 반응물 | 6-Chloro-7,8-dimethyl-[1,2,4]triazolo[4,3-B]pyridazin-3-amine | HCID 58045804 | — |
| 용매 | Diethylamine | HCID 8021 | — |
| 생성물 | N*6*,N*6*-Diethyl-7,8-dimethyl-[1,2,4]triazolo[4,3-b]pyridazine-3,6-diamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08076336B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-cf89ee8961294bbca38c75059dd07309 |
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| 출처 메모 | uspto-grants-2011_12 |
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