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HRID 6599作成日:2026年10月23日

2-Dimethylaminopyridine → 2',3'-Difluoro-4'-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyloxycarbonyl]-phenyl ester

https://huagongshe.com/ja/reaction/6599

反応式

関与物質

役割名称HCID仕込み量
反応物2-DimethylaminopyridineHCID 21885—
反応物4'-(4-Butoxybutoxy)-2',3'-difluorobiphenyl-4-carboxylic acidHCID 22016253—
反応物(R)-(+)-1,1,1-trifluoro-2-octyl 4-benzyloxybenzoateHCID 22850730—
溶媒TetrahydrofuranHCID 8028—
溶媒DiisopropylcarbodiimideHCID 12734—
生成物2',3'-Difluoro-4'-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyloxycarbonyl]-phenyl esterHCID 5867963465%

反応手順

To a solution of 4′-(4-butoxybutoxy)-2′,3′-difluorobiphenyl-4-carboxylic acid (27) (1 equi.), (4-hydroxybenzoic acid (R)-1-trifluoromethyl-heptyl ester (13, Scheme 7) (1 equi.), and DMAP (dimethylaminopyridine) (0.1 equi.) in THF (25 mL/mmole), DIC (diisopropyl carbodiimide) (1.2 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc/hexanes) gave 2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethylheptyloxycarbonyl]-phenyl ester (28) as a white solid (65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07083832B2
出典データセットuspto-grants-2006_08
ORD IDord-66e871d4bd824865a6d3a12ea3da7ade
出典メモuspto-grants-2006_08