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Carbon Disulfide → 1-(4-Isothiocyanatophenyl)-4-(4-methoxyphenyl)piperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | Diisopropyl Ether | HCID 7914 | — |
| 反応物 | Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)- | HCID 154406 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1-(4-Isothiocyanatophenyl)-4-(4-methoxyphenyl)piperazine | HCID 15581899 | — |
反応手順
To a stirred and cooled (ice-bath) mixture of 5 parts of N,N'-methanetetraylbis[cyclohexanamine], 25.2 parts of carbon disulfide and 40 parts of pyridine are added 6 parts of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine and the whole is stirred first for 1 hour in an ice-bath and further for 2 hours at room temperature. 35 Parts of 2,2'-oxybispropane are added and the whole is stirred for 30 minutes. The precipitated product is filtered off and crystallized from 4-methyl-2-pentanone. The product is filtered off again and recrystallized from 1,4-dioxane, yielding 2.45 parts of 1-(4-isothiocyanatophenyl)-4-(4-methoxyphenyl)piperazine; mp. 180.6° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04490530 |
| 出典データセット | uspto-grants-1984_12 |
| ORD ID | ord-78468c47499e4d4badf7e5169b0757d3 |
| 出典メモ | uspto-grants-1984_12 |