化工社化工社 化学情報印刷レポート · 研究参考用
HRID 21896作成日:2026年10月26日
Hydrochloric Acid → trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxy-N-benzenesulphonylcyclohexanecarboxamide
https://huagongshe.com/reaction/21896
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Benzenesulfonamide | HCID 7370 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxycyclohexanecarboxylic acid | HCID 15728507 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxy-N-benzenesulphonylcyclohexanecarboxamide | HCID 15239633 | 6.7% |
反応手順
trans-2-(4,6-Dimethoxypyrimidin-2-yl)oxycyclohexanecarboxylic acid (1.0 g), prepared as in Example 11, in dry tetrahydrofuran (10 ml) was added dropwise to a stirred solution of 1,1-carbonyldiimidazole (0.57 g) in dry tetrahydrofuran (10 ml) under nitrogen. The reaction mixture was stirred 30 minutes at ambient temperature, heated to reflux for 30 minutes and cooled to ambient temperature. Benzenesulphonamide (0.56 g) was added followed by dropwise addition of 1,8-diazabicyclo (5.4.0) undec-7-ene (0.54) in dry tetrahydrofuran (5 ml). The reaction mixture was stirred for 24 hours at ambient temperature, refluxed for 6 hours then poured into 1N hydrochloric acid (80 ml) and extracted with 3×100 ml portions of diethyl ether. The combined ether extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed on silica-gel, using a 2:1 dichloromethane/ethyl acetate eluant, to give 100 mg of the title compound, melting point 175° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05426090 |
|---|
| 出典データセット | uspto-grants-1995_06 |
|---|
| ORD ID | ord-66998b7f00e74f96b7a19de6d7beba6e |
|---|
| 出典メモ | uspto-grants-1995_06 |
|---|