関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nefazodone | HCID 4449 | — |
| 反応物 | Benzene, (2-bromoethoxy)- | HCID 68526 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | Nefazodone Hydrochloride | HCID 54911 | 30.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04575555 |
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| 出典データセット | uspto-grants-1986_03 |
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| ORD ID | ord-b87a59b3c9564f8aacedc74b1ae53c34 |
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| 出典メモ | uspto-grants-1986_03 |
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