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) (2.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (1.0 ml) and 3-(chloromethyl)benzoyl chloride (compound B) (2.0 g) were added to the solution at room temperature, and the mixture was stirred at that temperature for 3 hr. After the completion of the reaction, distilled water was added thereto, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with a saturated aqueous sodium chloride solution, was dried over sodium sulfate and was then concentrated to give methyl 5-bromo-2-[3-(chloromethyl)benzoyl]aminobenzoate as a useful intermediate (3.32 g, yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134015B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-5d25bbfcc2ba47f2b649f4b3bdba1b39 |
| Source note | uspto-grants-2012_03 |