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HRID 266728作成日:2026年10月27日

Ammonia → 4-(4-(4-Pyridyl)piperazin-1-yl)phenol

https://huagongshe.com/reaction/266728

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物WaterHCID 962—
反応物4-[4-(4-Pyridyl)piperazin-1-yl]anisoleHCID 14986902—
溶媒Hydrogen BromideHCID 260—
生成物4-(4-(4-Pyridyl)piperazin-1-yl)phenolHCID 1498690395.6%

反応手順

The product from step (i) (1.5 g) in concentrated hydrobromic acid (30 ml) was heated under argon at 130°-135° C. for 21/2 hours. The solution was cooled, poured into water (150 ml) and basified with aqueous ammonia. The precipitate was filtered, washed with water and dried to give 4-[4-(4-pyridyl)piperazin-1-yl]phenol (1.36 g) as a solid: m.p. 310°-312° C.; NMR(d6DMSO) δ 8.2(2H,d); 6.8(4H,m); 6.66(2H,d); 3.45(4H,m); 3.08(4H,m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05652242
出典データセットuspto-grants-1997_07
ORD IDord-b813d3b52b0240bb94c2a75089c2e209
出典メモuspto-grants-1997_07