참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropylamine | HCID 6363 | — |
| 반응물 | 1-Phenyl-2-(2-pyridinyl)ethanone | HCID 74179 | — |
| 반응물 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 반응물 | Acetic acid, 2-hydrazinyl-, ethyl ester, hydrochloride (1:1) | HCID 11593468 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | Ethyl-5-phenyl-4-(2-pyridinyl)-1H-pyrazole-1-acetate | HCID 15086050 | 61.6% |
반응 단계
A solution of 26 g (0.132 mol) of 1-phenyl-2-(2-pyridinyl)ethanone and 19.3 mL (0.145 mol) of dimethylformamide dimethylacetal in 100 mL of methyl t-butyl ether was refluxed 4 hr. Because TLC on silica gel with 10% isopropylamine in ethyl acetate showed little reaction, another 20 mL of DMF dimethylacetal was added and the solution refluxed a further 6 hr. The solvent was stripped and the resulting crude, oily β-ketoenamine was dissolved in 400 mL of ethanol. The ethanol solution was heated to 40° with 22 g (0.143 mol) of ethyl hydrazinoacetate hydrochloride for about 1.5 hr. The solvent was stripped, and the resulting impure product was dissolved in a small amount of methylene dichloride and applied to a column of 850 g of silica gel. The column was eluted with 2:1 hexane-ethyl acetate to yield 25 g of yellow solid product, mp 98°-100° C. after evaporation of the solvent.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04925857 |
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| 출처 데이터셋 | uspto-grants-1990_05 |
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| ORD ID | ord-60b73e2681bd476d9b806b0a330e7602 |
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| 출처 메모 | uspto-grants-1990_05 |
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