HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | (2-Aminophenyl)(pyridin-4-yl)methanone | HCID 14005182 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine | HCID 18175249 | — |
Reaction Steps
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+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605634B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-63470f7b151e47ca901cfe17538a4025 |
| Source note | uspto-grants-2003_08 |