HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(((4-((5-Bromo-2-pyrimidinyl)oxy)-3-chlorophenyl)amino)carbonyl)-2-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Nitrobenzoyl isocyanate | HCID 12583438 | — |
| Reactant | 4-(5-Bromo-2-pyrimidinyloxy)-3-chloroaniline | HCID 13771440 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(((4-((5-Bromo-2-pyrimidinyl)oxy)-3-chlorophenyl)amino)carbonyl)-2-nitrobenzamide | HCID 128803 | 84.5% |
Reaction Steps
Into a flask, a solution obtained by dissolving 6.80 g of the above 4-(5-bromo-2-pyrimidinyloxy)-3-chloroaniline in 30 ml of dioxane, was introduced, and a solution obtained by dissolving 5.76 g of 2-nitrobenzoylisocyanate in 30 ml of dioxane, was dropwise added thereto, and then the mixture was reacted at room temperature for 9 hours. After the completion of the reaction, the product was poured into water, subjected to filtration and washed with hot water. The crystals thereby obtained were put into methanol, and stirred, and then subjected to filtration again, to obtain 9.42 g of the desired product having a melting point of from 234 to 236° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04727077 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-5d8975024a1740ce98c9290e59b3aec3 |
| Source note | uspto-grants-1988_02 |