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HRID 482787作成日:2026年10月26日

Nefazodone → Nefazodone Hydrochloride

https://huagongshe.com/reaction/482787

反応式

関与物質

役割名称HCID仕込み量
反応物NefazodoneHCID 4449—
反応物Benzene, (2-bromoethoxy)-HCID 68526—
反応物SodiumHCID 5360545—
溶媒O-XyleneHCID 7237—
生成物Nefazodone HydrochlorideHCID 5491130.7%

反応手順

The sodium salt is pulverized, suspended in 200 ml. of xylene and mixed with phenoxyethyl bromide (10.4 g., 0.052 mole) in 20 ml. of xylene. The resulting mixture is refluxed with stirring for a 64 hr. period and the hot reaction mixture filtered. The filtrate is concentrated under reduced pressure and residual material taken up in ether. Insolubles are collected and the ether filtrate concentrated to afford 22.9 g. (94%) of 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one as the free base. Purification of the product is carried out by acidifying a solution of the free base in ethanol with ethanolic hydrogen chloride, and crystallization to afford hydrated (0.25 mole) 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one hydrochloride, m.p. 175°-177° C. (30.7% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04575555
出典データセットuspto-grants-1986_03
ORD IDord-b87a59b3c9564f8aacedc74b1ae53c34
出典メモuspto-grants-1986_03