関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | 2-Methylquinoline-4,6-diamine | HCID 223995 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Jtc-801 | HCID 5311339 | 59% |
反応手順
To a solution of 2-[(4-ethylphenoxy)methyl]benzoic acid (1.13 g, 4.4 mmol) obtained in Preparation Example 2-1 in chloroform (20 ml) was added oxalyl chloride (0.6 ml, 6.8 mmol) and the mixture was stirred at room temperature for 1 hr. Then the reaction mixture was concentrated under reduced pressure. To the obtained acid chloride were added pyridine (20 ml) and 4,6-diamino-2-methylquinoline (623 mg, 4 mmol) obtained in Preparation Example 1-1 and the mixture was stirred at room temperature for 10 hr. To the reaction mixture was added an aqueous sodium hydrogencarbonate solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over sodium sulfate, and the solvent was evaporated. The obtained crude product was dissolved in ethanol and treated with active charcoal, and the solvent was evaporated. The obtained residue was dissolved in ethyl acetate and 1N hydrochloric acid-ether solution was added. The resulting precipitate was collected by filtration. The obtained solid was heated and dried under reduced pressure to give the title compound (1.06 g, 59%, pale-yellow crystals).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06410561B1 |
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| 出典データセット | uspto-grants-2002_06 |
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| ORD ID | ord-877dd52c90344404af587b56784ff73d |
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| 出典メモ | uspto-grants-2002_06 |
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