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HRID 562913作成日:2026年10月24日

Isopropyl iodide → Methyl 2-(3-cyano-4-isopropoxyphenyl)isonicotinate

https://huagongshe.com/ja/reaction/562913

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl iodideHCID 6362—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 2-(3-cyano-4-hydroxyphenyl)isonicotinateHCID 136368377—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-(3-cyano-4-isopropoxyphenyl)isonicotinateHCID 6699504195.2%

反応手順

In 5 ml of DMF were dissolved 82 mg of methyl 2-(3-cyano-4-hydroxyphenyl)isonicotinate and 66 mg of isopropyl iodide, and the resulting solution was heated at 80° C. for 3 hours in the presence of 72 mg of potassium carbonate and 10 mg of tetra-n-butylammonium bromide. The reaction solution was cooled and then diluted with water, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried and concentrated under reduced pressure. The resulting residue was washed with a mixed solvent (hexane:ethyl acetate=10:1) to obtain 91 mg of methyl 2-(3-cyano-4-isopropoxyphenyl)isonicotinate. (2) Then, 86 mg of the compound was dissolved in a mixed solution of 3 ml of methanol and 3 ml of THF, and 0.35 ml of a 1M aqueous sodium hydroxide solution was added thereto, followed by heating at 60° C. for 1 hour. After being cooled to room temperature, the resulting solution was diluted with diisopropyl ether and water and an aqueous layer was separated. The aqueous layer was neutralized with 1M hydrochloric acid and then extracted with ethyl acetate. After being washed with water, the organic layer was dried and concentrated under reduced pressure to obtain 55 mg of 2-(3-cyano-4-isopropoxyphenyl)isonicotinic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067446B2
出典データセットuspto-grants-2011_11
ORD IDord-f3e080e16a49494697220dc0092501c6
出典メモuspto-grants-2011_11