참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | 5,6-Diphenyl-3(2H)-pyridazinone | HCID 150976 | — |
| 반응물 | Methyl 9-bromononanoate | HCID 554142 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | methyl 6-oxo-3,4-diphenyl-1(6H)-pyridazinenonanoate | HCID 9931844 | 96.2% |
반응 단계
Sodium hydride (840 mg of a 60% dispersion in oil, 20 mmol) was washed twice with hexanes, covered with DMF (25 mL) and 5,6-diphenyl-3(2H)-pyridazinone (4 g, 16 mmol), obtained according to P. Schmidt, et al., Helvetica Chim. Acta., 37, 134-140 (1954), added. After gas evolution had ceased, the mixture was stirred at room temperature for 30 minutes before adding methyl 9-bromononanoate (4.45 g, 18 mmol). The mixture was heated briefly to 110° C. to give a solution and then allowed to cool before being stirred at room temperature for 1 hour. The mixture was diluted with water and extracted with diethyl ether (3×). The combined extracts were washed with water, dried over sodium sulfate and concentrated to leave an oil. Chromatography on a column of silica gel afforded methyl 6-oxo-3,4-diphenyl-1(6H)-pyridazine nonanoate (6.44 g, 95%) as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04992439 |
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| 출처 데이터셋 | uspto-grants-1991_02 |
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| ORD ID | ord-2de90a7cd6704c34a10f3605c9ea7f9c |
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| 출처 메모 | uspto-grants-1991_02 |
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