関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phenethyl bromide | HCID 7666 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Ether hydrobromide | HCID 86739792 | — |
| 反応物 | HCID 178480237 | HCID 178480237 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide | HCID 14032511 | 36% |
反応手順
To a stirred mixture of 0.86 g of sodium hydride (50% oil dispersion) in 50 ml of dimethylformamide was added, dropwise, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 15 ml of hot dimethylformamide. The reaction mixture was stirred at ambient temperature for 1 hr and then a solution of 3.33 g of (2-bromoethyl)benzene in 10 ml of dimethylformamide was added dropwise. The reaction mixture was stirred for 21/2 days at ambient temperature, cooled to 0°, and water was added dropwise. The mixture was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and a saturated hydrogen bromide/ether solution was added dropwise. The resultant solid was recrystallized two times from ethanol to yield 2.0 g (36%) of product, mp 163°-164° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04670447 |
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| 出典データセット | uspto-grants-1987_06 |
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| ORD ID | ord-21f347a238924514af23d85af2ba5572 |
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| 出典メモ | uspto-grants-1987_06 |
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