関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylamine | HCID 7912 | — |
| 反応物 | 2-Amino-1-butanol | HCID 22129 | — |
| 反応物 | Chlorine | HCID 24526 | — |
| 反応物 | 2,6-Dichloro-4-(trifluoromethyl)nicotinonitrile | HCID 2736726 | — |
| 生成物 | 2-Chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl)pyridine-3-carbonitrile | HCID 86653421 | 55% |
反応手順
Neat 3-cyano-2,6-dichloro-4-trifluoromethylpyridine (0.641 g, 6 mmol) was added by pipette at a dropwise rate over 3 minutes to 2-aminobutanol (1.5 g, 6 mmol). Di-isopropylamine (0.9 g, 7 mmol) was added after 10 minutes and the resultant mixture was heated in a sealed tube at 70° C. for 30 minutes to selectively displace the chlorine at position 6 before quenching in ice-cold water and extracted with dichloromethane. Organic extracts were washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue was washed with diethylether and the resultant solid was used in the next step without further purification. 2-Chloro-6-(2-hydroxybutylamino)-4-(trifluoromethyl)pyridine-3-carbonitrile was isolated in 55% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09131694B2 |
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| 出典データセット | uspto-grants-2015_09 |
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| ORD ID | ord-6dfd08c581e74732b0ee67d9ccb2f6a6 |
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| 出典メモ | uspto-grants-2015_09 |
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