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Chloroform → 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| 反応物 | (2-Aminophenyl)(pyridin-4-yl)methanone | HCID 14005182 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine | HCID 18175249 | — |
反応手順
4-Fluorobenzoyl chloride (78.0 mg, 0.55 mmol) was added to 4-(2-aminobenzoyl)pyridine (12) (100 mg, 0.50 mmol), triethylamine (0.35 mL, 2.52 mL), and chloroform (5.0 mL) at 23° C. under argon. After 24 h at 23° C., the reaction was poured into water (50 mL), extracted with ethyl acetate (3×50 mL), and dried (MgSO4). After concentration in vacuo, the residue was purified by flash chromatography (ethyl acetate:methylene chloride 1:1) to afford 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine (14): Mass Spectrum (CI) 321 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06605634B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-63470f7b151e47ca901cfe17538a4025 |
| 出典メモ | uspto-grants-2003_08 |