HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 23107570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Veratroyl chloride | HCID 77070 | — |
| Reactant | Methyl 2-amino-5-bromobenzoate | HCID 736224 | — |
| Product | HCID 23107570 | HCID 23107570 | — |
Reaction Steps
Methyl 2-amino-5-bromobenzoate (compound A) (3.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (2.1 ml) and 4-(chloromethyl)benzoyl chloride (compound B) (2.2 ml) were added to the solution at room temperature, and the mixture was stirred at that temperature for one hr. After the completion of the reaction, distilled water was added, followed by separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated to give methyl 5-bromo-2-[3-(chloromethyl)benzoyl]aminobenzoate as a useful intermediate (4.90 g, yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134015B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-ee110e8d1b1040b6b8464c4361847445 |
| Source note | uspto-grants-2012_03 |