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3,4-Dichlorobenzyl chloride → 2-[1-(3,4-Dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride | HCID 66924378 | — |
| 生成物 | 2-[1-(3,4-Dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile | HCID 66924343 | 73% |
反応手順
A mixture of 2-fluoro-6-(piperidin-4-ylmethoxy)-benzonitrile hydrochloride (240 mg; 0.89 mmol) (Example 126, Step 3) was heated with 3,4-dichlorobenzyl chloride (0.15 mL; 2.0 mmol) and triethylamine (0.3 mL; 2.0 mmol) to 50° C. 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 material was purified by chromatography using 0.5-2% methanol/DCM gradient to afford 2-[1-(3,4-dichloro-benzyl)-piperidin-4-ylmethoxy]-6-fluoro-benzonitrile as a yellow oil. (280 mg; 73% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09067897B2 |
| 出典データセット | uspto-grants-2015_06 |
| ORD ID | ord-9575f5bd241f4c0abc2c5beb1af07039 |
| 出典メモ | uspto-grants-2015_06 |