HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → [1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitro-phenyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | 2-Methyl-4-nitroaniline | HCID 7441 | — |
| Reactant | 6-(2-Chloro-benzoimidazol-1-yl)-pyrimidin-4-ylamine | HCID 59822455 | — |
| Product | [1-(6-Amino-pyrimidin-4-yl)-1H-benzoimidazol-2-yl]-(2-methyl-5-nitro-phenyl)-amine | HCID 15949047 | — |
Reaction Steps
A solution of 6-(2-chloro-benzoimidazol-1-yl)-pyrimidin-4-ylamine (110 mg, 0.45 mmol), 2-methyl-4-nitro-phenylamine (103 mg, 0.68 mmol), and MeSO3H (58.0 μL, 0.9 mmol) in 1,3-dimethyl-2-imidazolidinone (0.2 ml) is heated at 90° C. After stirring for 2 hours, the reaction mixture is cooled to room temperature and is treated with water (5 mL). Solid is collected via filtration and further purified by flash chromatography on silica gel (0% MeOH/Dichloromethane to 10% MeOH/Dichloromethane gradient). The title compound is obtained as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426404B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-d16c29f5fe4a438bad1e80d39fea7ea1 |
| Source note | uspto-grants-2013_04 |