HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | pyridine-3-sulfonamide | HCID 232710 | — |
| Reactant | Methyl (4,6-dimethylpyrimidin-2-yl)carbamate | HCID 13278970 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide | HCID 13533294 | — |
Reaction Steps
To a slurry of 3-pyridinesulfonamide (1 m mole) in methylene chloride is added 2 m mole of trimethylaluminum. Following methane evolution, the reaction mixture becomes homogeneous, whereupon 1 m mole of methyl (4,6-dimethylpyrimidin-2-yl)carbamate is added, and stirring is continued for 66 hours. Aqueous acetic acid is added and the product is extracted into methylene chloride. The solvent is evaporated and the product is isolated by trituration on chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04544401 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-4aa4af493cc943bd9a2c9a0cd82aa833 |
| Source note | uspto-grants-1985_10 |