참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Phosphine oxide, (chloromethyl)dimethyl- | HCID 74224 | — |
| 반응물 | 1-phenyl-3-(1-piperazinyl)-1H-indazole | HCID 9795644 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-Phenyl-1H-indazole | HCID 304268 | — |
반응 단계
A stirred mixture of 4.3 g of 1-phenyl-3-(1-piperazinyl)-1H-indazole (prepared as in Example 2), 2.3 g of potassium carbonate, and 2.3 g of chloromethyldimethylphosphine oxide in 75 ml of dimethylformamide was heated at 90°, under nitrogen, for 16 hrs. Additional chloromethyldimethylphosphine oxide (0.6 g) was added, and the reaction mixture heated at 90° C. for 24 hrs. The reaction mixture was poured into water and the aqueous solution extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated to an oil. Flash chromatography of the oil on silica gel, eluting with dichloromethane/methanol (10%) followed by concentration of the appropriate fractions and trituration with diethyl ether gave 2.5 g (45%) of 3-[4-(dimethylphosphinylmethyl)-1-piperazinyl)]-1-phenyl-1H-indazole.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04999356 |
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| 출처 데이터셋 | uspto-grants-1991_03 |
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| ORD ID | ord-27ab6c80aeed430cb91ad43d48f2b095 |
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| 출처 메모 | uspto-grants-1991_03 |
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