HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-bromo-N-cyclopropyl-2-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 4-Bromo-2-methylbenzoic acid | HCID 99570 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-bromo-N-cyclopropyl-2-methylbenzamide | HCID 22568840 | — |
Reaction Steps
A solution of 4-bromo-2-methylbenzoic acid and SOCl2 was refluxed for 3 hours, cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in 30 mL CH2Cl2 and combined with cyclopropyl amine (810.0 mg, 14.3 mmols) and pyridine (2.05 g, 26.0 mmols). The solution was stirred for 18 hours and then diluted with EtOAc before being washed with 5% aqueous HCl, saturated NaHCO3, and saturated aqueous NaCl. The solution was dried (MgSO4) and concentrated under reduced pressure leaving the title compound as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380256B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-be5d495ce3bd405fafaeb204e4640709 |
| Source note | uspto-grants-2002_04 |