関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5,6-Dimethyluracil | HCID 96031 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | 2-Hydroxybutanedinitrile | HCID 21253562 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 178467469 | HCID 178467469 | 71% |
反応手順
To dimethyl uracil (10.5 g, 75 mmol) in EtOH (75 mL) was added malonitrile (9.9 g, 150 mmol) and EtONa (2.5 M, 60 mL, 150 mmol). The mixture was refluxed for 2 h and the precipitates were collected and washed with EtOH. The solid was treated with 2N aqueous HCl and extracted with EtOAc to provide 2-ethoxy-6-hydroxy-nicotinonitrile (8.7 g, 71%). A portion of this material (8.2 g, 50 mmol) was dissolved in CH2Cl2 (75 mL) followed by addition of PhNTf2 (19.6 g, 55 mmol) and Et3N (6.06 g, 60 mmol). The mixture was allowed to stir at ambient temperature overnight and washed with water and purified by column chromatography to provide trifluoro-methanesulfonic acid 5-cyano-6-ethoxy-pyridin-2-yl ester (15.9 g, coeluted with PhNHTf). A portion of this material (9.5 g, impure) was dissolved in MeOH (40 mL) followed by addition of PdCl2CH2Cl2dppf (1.4 g, 1.7 mmol) and Et3N (6.5 g, 65 mmol). The mixture was heated at 50° C. under CO (100 psi) for 6 h. The mixture was purified by column chromatography to provide 5-cyano-6-ethoxy-pyridine-2-carboxylic acid methyl ester (2 g, 32% over 2 steps). A portion of this material (1.5 g, 7.3 mmol) was dissolved in EtOH/H2O (5:3, 15 mL) followed by addition of LiOH (640 mg, 15 mmol). The mixture was stirred for 30 min and 2N aqueous HCl was added to adjust the acidity to pH of 1. Precipitates were collected and washed to provide 5-cyano-6-ethoxy-pyridine-2-carboxylic acid (1.0 g, 71%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07888374B2 |
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| 出典データセット | uspto-grants-2011_02 |
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| ORD ID | ord-a3c3e536e6e34ef581c61898c8cee0de |
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| 出典メモ | uspto-grants-2011_02 |
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