HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → N-(2-Bromo-6-methoxy-4-methyl-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-(2-bromo-6-methoxy-4-methyl-3-pyridinyl)-2-chloro-3-pyridinecarboxamide | HCID 19960021 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-Bromo-6-methoxy-4-methyl-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide | HCID 19960032 | 44.2% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A mixture of N-(2-bromo-6-methoxy-4-methyl-3-pyridinyl)-2-chloro-3-pyridinecarboxamide (2.1 g), dioxane (10 ml), and ethylamine (0.5 g) was heated to 140° C. in a sealed tube for 5 hours. The cooled mixture was diluted with ethyl acetate, washed with water, and the organic phase was dried (anhydrous magnesium sulfate) and concentrated. The product was purified on a silica gel column (methylene chloride/ethyl acetate, 99:1) and crystallized by trituration with diisopropyl ether to give 0.95 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05366972 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-b78d061dc707459e9140f7cae25b93d4 |
| Source note | uspto-grants-1994_11 |