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Triethylamine → 2-[1-(3-Iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-Iodobenzoyl chloride | HCID 74378 | — |
| 反応物 | 2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride | HCID 66924378 | — |
| 生成物 | 2-[1-(3-Iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile | HCID 66924441 | 95% |
反応手順
A mixture of 2-fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride (200 mg; 0.7 mmol) (Example 123, Step 3) was stirred at room temperature with 3-iodobenzoyl chloride (187 mg; 0.7 mmol) and triethylamine (0.3 mL; 2.1 mmol) for 16 hours. Reaction was cooled and quenched with dilute HCl and mixture extracted with ethyl acetate (2×20 mL). Combined organics washed with water, saturated sodium bicarbonate, brine and dried over Na2SO4. Crude solid was obtained as 2-[1-(3-iodo-benzoyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile. (310 mg; 95% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07888366B2 |
| 出典データセット | uspto-grants-2011_02 |
| ORD ID | ord-1214fe052fb740e9b9578e18bc2f4443 |
| 出典メモ | uspto-grants-2011_02 |