Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1067518생성일: 2026년 10월 23일
Sodium hydride → 6-[2-[2-[4-(Diphenylmethyl)piperazino] ethoxy]ethoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine
https://huagongshe.com/ko/reaction/1067518
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Decloxizine | HCID 71135 | — |
| 반응물 | 6-Chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine | HCID 22989227 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-[2-[2-[4-(Diphenylmethyl)piperazino] ethoxy]ethoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine | HCID 22989283 | 50.9% |
반응 단계
160 mg of 60% sodium hydride in oil was suspended in 20 ml of tetrahydrofuran; 1.20 g of 4-(diphenylmethyl)-1-[2-(2-hydroxyethoxy)ethyl]piperazine was added, followed by heating and refluxing for 1 hour. After cooling, 610 mg of 6-chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 1 hour. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate:methanol (10:1). The desired fraction was collected; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 790 mg of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06248740B1 |
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| 출처 데이터셋 | uspto-grants-2001_06 |
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| ORD ID | ord-ef8602045b2f469eaa20233b91283dd4 |
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| 출처 메모 | uspto-grants-2001_06 |
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