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HRID 2242作成日:2026年10月24日

Triethylamine → 4-[2-[4-(4-Pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetic acid monohydrochloride

https://huagongshe.com/ja/reaction/2242

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Chloropyridine hydrochlorideHCID 81852—
反応物Methyl 4-[2-(piperazin-2-one-1-yl)acetyl]-phenoxyacetateHCID 18918321—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物4-[2-[4-(4-Pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetic acid monohydrochlorideHCID 7007911740.7%

反応手順

A solution of methyl 4-[2-(piperazin-2-one-1-yl)acetyl]-phenoxyacetate (0.347 g), 4-chloropyridine hydrochloride (0.19 g) and triethylamine (0.178 g) in water (8 ml) and dioxan (1 ml) was heated on a steam bath for 2 hours and then evaporated to dryness. The residue was triturated with water (2 ml) and filtered. The solid thus obtained was recrystallised from water to give the title compound (0.187 g), m.p. 275°-277° C.; NMR(d6DMSO δ 8.33(2H,d), 8.0(2H,d), 7.21(2H,d), 7.1(2H,d), 4.97(2H,s), 4.81(2H,s), 3.94(2H,m), 3.59(2H,m); m/e 370(H+H)+ ; calculated for C19H20N3O5Cl. 0.75 H2O: C, 54.4; H, 5.0; N, 10.0. Found: C, 54.5; H, 5.3; N, 9.5%.

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-35a8c2a4b4bc4caeaaf6b411adca67fe
出典メモuspto-grants-1998_03