関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N,N-Dimethylaniline | HCID 949 | — |
| 反応物 | Piperazine | HCID 4837 | — |
| 反応物 | 3-(3-Methoxypropoxy)-1-propanol | HCID 66984 | — |
| 反応物 | 4-Chloro-3-methoxy-2-methylpyridine | HCID 10583046 | — |
| 生成物 | 1-(3-Methoxy-2-methyl-4-pyridyl)piperazine | HCID 66835613 | 94.1% |
反応手順
4-Chloro-3-methoxy-2-methyl-pyridine (0.47 g, 3 mmol) was mixed with dipropyleneglycolmonomethylether (3 ml), piperazine (1.1 g, 7.2 mmol) and N,N-dimethylaniline (0.36 g, 3 mmol) and stirred at 140° C. for 72 hours. The solvent was removed under reduced pressure and the residue was purified by column chromatography (prepacked silica column, gradient ethyl acetate/methanol with the addition of 1% ammonia). The raw product was dissolved in 1M NaOH and extracted with a mixture of diethylether, dichloromethane and ethylacetate (1:1:1) several times. The combined organic phases were washed with water, dried over sodium sulfate, and the solvent was removed under reduced pressure to yield 585 mg of a yellow solid (2.8 g, 94%). MS (APCI): m/z=208.0 [M+1]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08883791B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-fd595ac2c5bc423eb5643a5e9bd250f5 |
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| 出典メモ | uspto-grants-2014_11 |
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