Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397556생성일: 2026년 10월 24일
Diisopropylethylamine → 6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazine
https://huagongshe.com/ko/reaction/397556
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 6-Chloro-[1,2,4]triazolo[4,3-b]pyridazine | HCID 313624 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 4-(Diphenylmethoxy)-1-piperidinepropaneamine | HCID 10969393 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | 6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazine | HCID 15524150 | 48.8% |
반응 단계
0.464 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine and 1.26 g of 4-(diphenylmethoxy)-1-piperidinepropanamine were suspended in 20 ml of 1-butanol; 0.62 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 12 hours. After ice water and sodium hydrogen carbonate were added, the reaction mixture was extracted with ethyl acetate; the extract was washed with saturated saline and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (90:10:1). The desired fraction was collected and concentrated; the crystal obtained was washed with ethyl acetate and dried to yield 0.648 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06610694B1 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-4d3147e3bb5844ada7c54f1b19c9dd47 |
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| 출처 메모 | uspto-grants-2003_08 |
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