HuagongsheHuagongshe Chemistry Print Report · For research reference only
n-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide → (2-Amino-3,4,5-trimethoxyphenyl)-n-(5 bromo(2-pyridyl))carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | n-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide | HCID 22596319 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2-Amino-3,4,5-trimethoxyphenyl)-n-(5 bromo(2-pyridyl))carboxamide | HCID 85783824 | 77.7% |
Reaction Steps
To a solution of the compound of N-(5-bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide (790 mg, 1.92 mmol) in ethyl acetate (5 ml) was added tin chloride (II) hydrate (1.73 g, 7.67 mmol). The mixture was stirred under reflux condition for 2 hrs. After filtered by Celite, the filtrate was added 1N sodium hydroxide solution and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-3,4,5-trimethoxyphenyl)-N-(5-bromo(2-pyridyl))carboxamide (570 mg, 77%). MS found for C15H16BrN3O4 M+=382, (M+2)+=384.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108922B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-cebf6d999fb54efda168bf6643d08c58 |
| Source note | uspto-grants-2015_08 |