化工社化工社 化学情報印刷レポート · 研究参考用
3-Fluorobenzyl chloride → 1-(3-fluorobenzyl)-2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Fluorobenzyl chloride | HCID 9974 | — |
| 反応物 | 18-Crown-6 | HCID 28557 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | 2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine | HCID 67141589 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(3-fluorobenzyl)-2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine hydrochloride | HCID 67142860 | 10% |
反応手順
18-Crown-6 (2.5 mg, 0.0097 mmol) and potassium tert-butoxide (33 mg, 0.291 mmol) were added to a solution of 2,3-dimethyl-7-(4-vinylphenyl)-1H-pyrrolo[2,3-c]pyridine (24 mg, 0.097 mmol) prepared in Example 242 in anhydrous tetrahydrofuran (0.5 ml). The reaction mixture was stirred for 30 minutes at room temperature and 3-fluorobenzyl chloride (20 μl, 0.16 mmol) was added thereto. The reaction mixture was stirred overnight and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography. The resulting product was dissolved in ethyl acetate, saturated with hydrochloric acid gas, and then filtered to give 3.8 mg of the titled compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07662832B2 |
| 出典データセット | uspto-grants-2010_02 |
| ORD ID | ord-95ea7496bed34927bef4b3cdc34fb111 |
| 出典メモ | uspto-grants-2010_02 |