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HRID 1480089作成日:2026年10月27日

Carbon Dioxide → 5-Cyclopropyl-4-cyclopropylmethoxy-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1480089

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物2-(Dimethylamino)ethanolHCID 7902—
反応物3-Cyclopropyl-4-(cyclopropylmethoxy)pyridineHCID 90203944—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒HexaneHCID 8058—
生成物5-Cyclopropyl-4-cyclopropylmethoxy-pyridine-2-carboxylic acidHCID 9020380966%

反応条件

温度-15 °C

反応手順

To a solution of N,N-Dimethylethanolamine (CAN 108-01-0, 2.372 g, 3.08 mL, 30.6 mmol) in hexane cooled at −15° C. under an argon atmosphere was slowly added BuLi 1.6M in Hexane (38.2 mL, 61.1 mmol). The reaction was stirred at −15° C. during 20 minutes and was then cooled down to −78° C. before addition of 3-cyclopropyl-4-cyclopropylmethoxypyridine (Example 42b, 2.314 g, 12.2 mmol). The reaction was stirred 1 hour at −78° C. followed by addition of carbon dioxide (2.09 g, 47.6 mmol) (pellets from a dry ice dispenser) into the mixture. A white precipitate formed and the reaction was slowly warmed up to −20° C. The reaction was quenched with water, stirred 5 minutes and the volatiles were removed in vacuo. The residue was suspended into ethylacetate and extracted with 19 mL of a 2.0M aqueous solution hydrochloric acid. The organic phase was collected, dried over sodium sulfate and evaporated down to dryness to give an yellow oil. The former oil was dissolved in diethylether which gave a white precipitate. The suspension was stored at 0° C. for 1 hour and the solution was separated from the white solid. The white solid was dried under high vacuum to give the titled compound (815 mg, 66%). MS (ESI, m/z): 234.2 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09409866B2
出典データセットuspto-grants-2016_08
ORD IDord-b3a67b3dd73146539c71f0bea78407be
出典メモuspto-grants-2016_08