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HRID 1640200作成日:2026年10月27日

Hydrochloric Acid → 7-[(2-Chloropyridin-4-yl)oxy]-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

https://huagongshe.com/reaction/1640200

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Cesium carbonateHCID 10796—
反応物2-Chloro-4-nitropyridineHCID 735152—
反応物7-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 14541268—
溶媒DimethylformamideHCID 6228—
生成物7-[(2-Chloropyridin-4-yl)oxy]-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 5805521152.1%

反応手順

A mixture of 7-hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (5.62 g, 29.2 mmol); 2-chloro-4-nitropyridine (5.10 g, 32.2 mmol) and cesium carbonate (28.6 g, 87.7 mmol) in DMF (150 mL) was heated at 50° C. for 5 hr. The reaction mixture was allowed to cool to rt and acidified to pH 3 by addition of 1N HCl. The mixture was extracted with EtOAc and the organic solutions were combined, washed with water, dried over Na2SO4 and evaporated. The residue was adsorbed onto silica and purified by filtration through a pad of silica. The product was then triturated with EtOAc to give 7-[(2-chloropyridin-4-yl)oxy]-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (4.62 g, 52.0%). LCMS: (FA) ES+ 304.1, ES− 302.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08110687B2
出典データセットuspto-grants-2012_02
ORD IDord-bf3a1acc90354465b1e8cdbb4a1fe2ab
出典メモuspto-grants-2012_02