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HRID 2187601作成日:2026年10月25日

Methane → Jtc-801

https://huagongshe.com/reaction/2187601

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物EthanolHCID 702—
反応物Oxalyl chlorideHCID 65578—
反応物2-Methylquinoline-4,6-diamineHCID 223995—
反応物Sodium BicarbonateHCID 516892—
溶媒PyridineHCID 1049—
生成物Jtc-801HCID 531133959%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06410561B1
出典データセットuspto-grants-2002_06
ORD IDord-877dd52c90344404af587b56784ff73d
出典メモuspto-grants-2002_06