化工社化工社 化学情報印刷レポート · 研究参考用
alpha-Chloro-o-xylene → 2,3-Dimethyl-8-(2-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | alpha-Chloro-o-xylene | HCID 11093 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 8-Amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide mesylate | HCID 18357435 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2,3-Dimethyl-8-(2-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxamide | HCID 9861426 | 13.2% |
反応手順
8-Amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxamide mesylate (1.0 g, 2.7 mmol), α-chloro-o-xylene (0.38 g, 2.7 mmol) and diisopropylethylamin (0.76 g, 5.9 mmol) in dimethylformamide (7 ml) were stirred at 50° C. for 7 h and at room temperature for 72 h. The solvent was evaporated and the residue was treated with a mixture of methylene chloride, water and a small amount of diisopropylethylamin. The solid that formed was isolated by filtration and washed with ethylacetate to give 0.11 g (13%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06313137B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-5fce369b50d845558544c18f95a8161d |
| 出典メモ | uspto-grants-2001_11 |