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HRID 614834作成日:2026年10月27日

4-(Phenoxymethyl)piperidine → 2-Amino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-3-nitrobenzene

https://huagongshe.com/reaction/614834

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Phenoxymethyl)piperidineHCID 3017444—
反応物1-(2-Amino-3-nitrophenoxy)-2,3-epoxypropaneHCID 11344838—
溶媒EthanolHCID 702—
生成物2-Amino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-3-nitrobenzeneHCID 21327312—

反応手順

A mixture of 40.0 g. 1-(2-amino-3-nitrophenoxy)-2,3-epoxypropane, 36.2 g. 4-phenoxymethylpiperidine and 450 ml. ethanol is stirred for 18 hours at ambient temperature and the solution thereby obtained of 2-amino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-3-nitrobenzene (m.p. 117°-118° C.) is subsequently hydrogenated at ambient temperature in the presence of 1.0 g. platinum oxide. After filtration, the filtrate obtained is acidified with dilute hydrochloric acid, evaporated and the evaporation residue redissolved in ethanol/ethyl acetate. There are obtained 72.3 g. 2,3-diamino-1-[2-hydroxy-3-(4-phenoxymethylpiperidino)-propoxy]-benzene trihydrochloride (81% of theory) in the form of an amorphous substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04146630
出典データセットuspto-grants-1979_03
ORD IDord-1c919157d63b4789acda1d6d8b1b2d84
出典メモuspto-grants-1979_03