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Triethylamine → N-(3-chloro-4-(3-chlorophenoxy)phenyl)picolinamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Picolinoyl Chloride Hydrochloride | HCID 135033 | — |
| 反応物 | 3-Chloro-4-(3-chlorophenoxy)aniline | HCID 17605534 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(3-chloro-4-(3-chlorophenoxy)phenyl)picolinamide | HCID 42645239 | 51% |
反応手順
According to Scheme 3 Step 3: Picolinoyl chloride hydrochloride (1.52 mmol, 271 mg) and Et3N (3.05 mmol, 0.42 mL) were added sequentially to a solution of 3-chloro-4-(3-chlorophenoxy)aniline (1.02 mmol, 258 mg) in DCM (6 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. The organic phase was washed with a saturated solution of NaHCO3 and with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure. The crude product was purified by flash chromatography over silica gel using cyclohexane/AcOEt (90:10) as eluent to afford N-(3-chloro-4-(3-chlorophenoxy)phenyl)picolinamide (0.52 mmol, 187 mg, 51%) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524726B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-4dd49d5ee1784637a7cfe86cc55f2823 |
| 出典メモ | uspto-grants-2013_09 |