Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1649101생성일: 2026년 10월 26일
Phosgene → 4,5-dihydro-5-methyl-6-[p-(1-methylprop-2-ynyloxycarbonylamino)-phenyl]-3(2H)-pyridazinone
https://huagongshe.com/reaction/1649101
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | 3-Butyn-2-ol | HCID 16239 | — |
| 반응물 | Ici 109,081 | HCID 161928 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 4,5-dihydro-5-methyl-6-[p-(1-methylprop-2-ynyloxycarbonylamino)-phenyl]-3(2H)-pyridazinone | HCID 12848792 | 23.1% |
반응 단계
3.5 g (49.9 millimoles) of 1-methylprop-2-ynol are added dropwise to a stirred solution of 9.9 g (100 millimoles) of phosgene in 100 ml of absolute ether at -10° C. The reaction solution is then stirred for 1 hour at -10° C. followed by one hour at room temperature, and the excess phosgene is removed by means of a dry stream of nitrogen, after which the ether is removed under reduced pressure at room temperature. The 1-methylprop-2-ynyl chloroformate which is left (5.9 g) is reacted with 5.0 g (24.6 millimoles) of 6-(p-aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone by the method described in Example 31. The reaction mixture is also worked up as described in Example 31. After recrystallizing the product first from ethanol/water, then from ethyl acetate/petroleum ether and finally from dimethylformamide/water, 1.7 g (23% of theory) of 4,5-dihydro-5-methyl-6-[p-(1-methylprop-2-ynyloxycarbonylamino)-phenyl]-3( 2H)-pyridazinone are obtained as colorless crystals of melting point 206°-207° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04415571 |
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| 출처 데이터셋 | uspto-grants-1983_11 |
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| ORD ID | ord-a8a7ca19bc8648dd8ea81dd6ec1ce04a |
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| 출처 메모 | uspto-grants-1983_11 |
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