関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Phosphine oxide, (chloromethyl)dimethyl- | HCID 74224 | — |
| 反応物 | 1-phenyl-3-(1-piperazinyl)-1H-indazole | HCID 9795644 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-Phenyl-1H-indazole | HCID 304268 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04999356 |
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| 出典データセット | uspto-grants-1991_03 |
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| ORD ID | ord-27ab6c80aeed430cb91ad43d48f2b095 |
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| 出典メモ | uspto-grants-1991_03 |
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