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HRID 516021作成日:2026年10月24日
Triethylamine → (R)-Methyl 6-(1-amino-4-methyl-1-oxopentan-2-ylamino)-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate
https://huagongshe.com/ja/reaction/516021
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (R)-2-Amino-4-methylpentanamide | HCID 7271815 | — |
| 反応物 | Methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate | HCID 58317716 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (R)-Methyl 6-(1-amino-4-methyl-1-oxopentan-2-ylamino)-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate | HCID 67239420 | 50.1% |
反応手順
A mixture of methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate (120.7 mg, 0.330 mmol), (R)-2-amino-4-methylpentanamide (67.1 mg, 0.515 mmol), and Et3N (0.1 mL, 0.717 mmol) in DMF (4 mL) was stirred at 60° C. for 14 h. Saturated aq NaHCO3 (20 mL) was added to the mixture, which was subsequently extracted with EtOAc (2×30 mL). The organic layers were washed with saturated aq NaHCO3 (20 mL), water (20 mL) and brine (20 mL), were dried over anhydrous Na2SO4, and filtered (DM1020). The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, hexanes/EtOAc=1/2) and then triturated with IPE to give the title compound (76 mg, 50%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09108970B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-34132de5c7ab469aa455ab8889860309 |
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| 出典メモ | uspto-grants-2015_08 |
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