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2-(Morpholin-4-yl)ethane-1-sulfonamide → N-(2-(Morpholino)ethanesulphonyl)-6-[N-(5-chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(Morpholin-4-yl)ethane-1-sulfonamide | HCID 12469816 | — |
| 反応物 | 6-[N-(5-Chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylic acid | HCID 18693249 | — |
| 生成物 | N-(2-(Morpholino)ethanesulphonyl)-6-[N-(5-chloro-2-(2-methylprop-2-en-1-yloxy)benzyl)-N-ethylamino]pyridazine-3-carboxamide | HCID 18693229 | — |
反応手順
The title compound was prepared by reacting 6-[N-(5-chloro-2-(2-methylprop-2-enyloxy)benzyl)-N-ethylamino]pyridazine-3-carboxylic acid (example 19) and 2-(morpholino)ethanesulphonamide using a similar method to that described in example 20 (yield 43%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06100258 |
| 出典データセット | uspto-grants-2000_08 |
| ORD ID | ord-65b49cecad3946bca411afd999ab13db |
| 出典メモ | uspto-grants-2000_08 |