HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 2-Chloro-N-[(5-chloro-4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Chloro-3-pyridinesulfonylisocyanate | HCID 13038435 | — |
| Reactant | 2-Amino-5-chloro-5,6-dimethylpyrimidine | HCID 70504730 | — |
| Product | 2-Chloro-N-[(5-chloro-4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide | HCID 20474842 | — |
Reaction Steps
To a stirred suspension of 1.4 g of 2-amino-5-chloro-5,6-dimethylpyrimidine in 20 ml of dry acetonitrile at room temperature is added 2.2 g of 2-chloropyridine-3-sulfonylisocyanate. The mixture is stirred for several hours, evaporated to dryness and the residue is mixed with 30 ml of water and enough 10% sodium hydroxide to adjust the pH to 11. This mixture is filtered and the filtrate adjusted to pH 7 by the addition of 10% hydrochloric acid and then refiltered. Acidification of this filtrate to pH 2 causes the desired compound to precipitate. The desired compound is filtered off and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04342587 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-ae7381d00f9e449496d9db8802d2fc34 |
| Source note | uspto-grants-1982_08 |