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Triethylamine → 4-Amino-N-[1-((4-amino-3-nitro-phenyl)-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-3,5-dichlorobenzenesulphonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Amino-3-nitro-phenylalanyl-(4-methyl-piperidine) | HCID 18659293 | — |
| 反応物 | 4-Amino-3,5-dichlorobenzene-1-sulfonyl chloride | HCID 18975981 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Amino-N-[1-((4-amino-3-nitro-phenyl)-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-3,5-dichlorobenzenesulphonamide | HCID 20089042 | — |
反応手順
3.06 g (10 mMol) of 4-amino-3-nitro-phenylalanyl-(4-methyl-piperidine) are dissolved in 100 ml of methylene chloride and combined with 2.8 ml (20 mMol) of triethylamine. Then at ambient temperature 3.1 g (12 mMol) of 4-amino-3,5-dichloro-benzenesulphonic acid chloride in 20 ml of methylene chloride is slowly added dropwise. After 2 hours the precipitate is suction filtered, washed with methylene chloride and dried at 70° C. For further purification the precipitate is suspended in 100 ml of ethanol, decocted and after cooling suction filtered again.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05391556 |
| 出典データセット | uspto-grants-1995_02 |
| ORD ID | ord-cffdfd0cd4324365967dd6d75102a36f |
| 出典メモ | uspto-grants-1995_02 |