HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-hydroxy-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(Benzyloxy)-5-hydroxybenzoic acid | HCID 24771944 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-hydroxy-2-[(phenylmethyl)oxy]-N-3-pyridinylbenzamide | HCID 51357514 | — |
Reaction Steps
Oxalyl chloride (1.08 ml, 12.28 mmol) was added to a mixture of 5-hydroxy-2-[(phenylmethyl)oxy]benzoic acid (1 g, 4.09 mmol) dissolved in dichloromethane. The mixture was stirred for 2 h, and then concentrated. The residue was dissolved in dichloromethane, and then added to a mixture of pyridin-3-amine (0.39 g, 4.09 mmol) and triethylamine (1.14 ml, 8.19 mmol) in dichloromethane. The mixture was stirred at 40° C. for 3 h. The mixture was filtered, and the filtrate was added to water (10 ml) and extracted with ethyl acetate (30 ml). The organic phase was concentrated to yield the title compound as a crude solid product. 0.72 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778939B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-a8fc597cb15046aeb2447e30592cd120 |
| Source note | uspto-grants-2014_07 |