化工社化工社 化学情報印刷レポート · 研究参考用
N-{4-[4-(4-Nitropyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide → N-{4-[4-(4-Aminopyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-{4-[4-(4-Nitropyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide | HCID 21283530 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-{4-[4-(4-Aminopyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide | HCID 21283535 | 59.7% |
反応手順
A solution of N-{4-[4-(4-nitropyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide (100 mg) in methanol (40 ml) was hydrogenated at 3 bar and 22° C. in the presence of 5% palladium on carbon (20 mg) until no more hydrogen was taken up. The catalyst was filtered off and the filtrate was evaporated. The residue was crystallised from aqueous methanol to give the title compound (55 mg), m.p. 225°-227° C. Found: C,55.50; H,6.04; N,19.66. C16H21N5O2S requires: C,55.31; H,6.09; N,20.16%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04788196 |
| 出典データセット | uspto-grants-1988_11 |
| ORD ID | ord-6871f8c47b3b466dbc9ba3ff4642ab27 |
| 出典メモ | uspto-grants-1988_11 |