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HRID 1640200생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1640200

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Cesium carbonateHCID 10796—
반응물2-Chloro-4-nitropyridineHCID 735152—
반응물7-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 14541268—
용매DimethylformamideHCID 6228—
생성물7-[(2-Chloropyridin-4-yl)oxy]-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 5805521152.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08110687B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-bf3a1acc90354465b1e8cdbb4a1fe2ab
출처 메모uspto-grants-2012_02