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HRID 1712362作成日:2026年10月25日

Biphenyl → Benzyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[3-(3-methoxypropoxy)-4-pyrrolidin-1-ylbenzyloxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/1712362

反応式

関与物質

役割名称HCID仕込み量
反応物BiphenylHCID 7095—
反応物PyrrolidineHCID 31268—
反応物Sodium t-butoxideHCID 23676156—
反応物Benzyl 3-[4-bromo-3-(3-methoxypropoxy)benzyloxy]-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylateHCID 68501756—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物Benzyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[3-(3-methoxypropoxy)-4-pyrrolidin-1-ylbenzyloxy]piperidine-1-carboxylateHCID 68505857—

反応条件

温度90 °C

反応手順

The mixture of 0.019 g of 2-di-t-butylphosphino)biphenyl, 0.005 g of palladium(II) acetate and 0.134 g of sodium tert-butoxide is admixed under argon with the solution of 0.831 g of benzyl 3-[4-bromo-3-(3-methoxypropoxy)benzyloxy]-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate and 0.100 ml of pyrrolidine in 7.0 ml of toluene. The reaction mixture is stirred at 90° C. over 16 hours, subsequently cooled, poured onto water (40 ml) and extracted with tert-butyl methyl ether (2×40 ml). The organic phases are washed with brine (40 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a white foam from the residue by means of flash chromatography (SiO2 60F). Rf=0.22 (1:1 EtOAc-heptane); Rt=5.40.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790715B2
出典データセットuspto-grants-2010_09
ORD IDord-a278ab4c3d0c4689a3cbf72f3a6d77cb
出典メモuspto-grants-2010_09