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HRID 2226作成日:2026年10月24日

Triphenylphosphine → Methyl 4-[1-(4-pyridyl)piperidin-4-yl]oxyphenoxyacetate

https://huagongshe.com/ja/reaction/2226

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Methyl 2-(4-hydroxyphenoxy)acetateHCID 602731—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物1-(Pyridin-4-yl)piperidin-4-olHCID 23447619—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-[1-(4-pyridyl)piperidin-4-yl]oxyphenoxyacetateHCID 18918626—

反応条件

温度4 °C

反応手順

Diethylazodicarboxylate (0.47 ml) was added dropwise over 30 minutes to a stirred mixture of 1-(4-pyridyl)-4-piperidinol (534 mg), methyl 4-hydroxyphenoxyacetate (546 mg), triphenylphosphine (787 mg) and dry THF (30 ml) in an atmosphere of argon and cooled to 4° C. After 1 hour at 4° C., the mixture was allowed to reach ambient temperature and stirred for 48 hours. The solvent was removed by evaporation and the residue purified by flash chromatography on silica eluting with 5% v/v methanol/dichloromethane. Recrystallisation from ethyl acetate/hexane gave the title compound, 532 mg, as a white solid: m.p. 74°-76° C.; NMR (d6DMSO) δ 8.15(2H, bd), 6.89(6H, m), 4.71(2H, s), 4.50(1H, m), 3.70(2H, m), 3.69(3H, s), 3.23(2H, m), 1.96(2H, m), 1.62(2H, m); m/e 343 (M+H)+ ; calculated for C19H22N2O4 : C, 66.7; H, 6.5; N, 8.2. found: C, 66.2; H, 6.7; N, 8.2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728701
出典データセットuspto-grants-1998_03
ORD IDord-0b7d284c41804ff1aae25f00491e423c
出典メモuspto-grants-1998_03