関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 反応物 | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | — |
| 反応物 | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| 反応物 | 2-(Trifluoromethyl)pyridine-4-boronic acid | HCID 45158880 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | (+-)-2-Butanol | HCID 6568 | — |
| 生成物 | (2'-(Trifluoromethyl)-2,4'-bipyridin-5-yl)methanamine | HCID 67208623 | — |
反応手順
To a flask containing (6-chloropyridin-3-yl)methanamine 33-2 (375 mg, 2.63 mmol), 2-(trifluoromethyl)pyridin-4-ylboronic acid 33-1 (500 mg, 2.63 mmol), Pd(OAc)2 (34 mg, 0.15 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (S-Phos) (124 mg, 0.30 mmol) and potassium phosphate (1.90 g, 9.00 mmol) under argon was added 2-butanol (4 mL). The mixture was stirred at 100° C. for 10 hours. After cooling to room temperature, the mixture was filtered through celite cake. The filtrate was diluted with ethyl acetate, washed with H2O and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 5% methanol containing ˜7N ammonia in dichloromethane to give (2′-(trifluoromethyl)-2,4′-bipyridin-5-yl)methanamine 33-3 as a yellow solid. MS m/z 254.1 (M+1)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09181235B2 |
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| 出典データセット | uspto-grants-2015_11 |
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| ORD ID | ord-3bcf7431285b4be586bd389a0b629ac8 |
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| 出典メモ | uspto-grants-2015_11 |
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