化工社化工社 化学情報印刷レポート · 研究参考用
1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → 2-(4-Tert-butyl-3,5-difluorophenoxy)-N-((1R)-1-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride | HCID 10986715 | — |
| 反応物 | N-{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochloride | HCID 66841089 | — |
| 反応物 | (4-tert-Butyl-3,5-difluorophenoxy)acetic acid | HCID 68804332 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 2-(4-Tert-butyl-3,5-difluorophenoxy)-N-((1R)-1-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide | HCID 57762923 | 37% |
反応手順
(4-tert-Butyl-3,5-difluorophenoxy)acetic acid (166 mg, 0.68 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (110 mg, 0.68 mmol), triethylamine (0.5 ml) and N-{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochloride (183 mg, 0.68 mmol) were mixed by the same procedure as described in Example 1(e) to give 115 mg (37%) of the title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07566739B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-958f5bc5e2c7406e8a469acd75604569 |
| 出典メモ | uspto-grants-2009_07 |