HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → 7-Chloro-3-(pyrid-2-yl)amino-4H-1,2,4-benzothiadiazine 1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 7-Chloro-3-methylsulfinyl-4H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 21197903 | — |
| Solvent | 3-Chlorotoluene | HCID 7931 | — |
| Product | 7-Chloro-3-(pyrid-2-yl)amino-4H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 11109629 | — |
Reaction Steps
7-Chloro-3-methylsulfinyl-4H-1,2,4-benzothiadiazine 1,1-dioxide (0.25 g) and 2-aminopyridine (0.25 g) in 3-chlorotoluene (5 mL) was heated at 150° C. for 1 h. After cooling, the white precipitate was collected by filtration and washed with diethylether. The insoluble material was dissolved in 1M NaOH (20 mL), treated with charcoal, filtered, and the filtrate was adjusted to pH 3 with 6N HCl. The precipitate was collected by filtration, washed with water, dissolved in hot DMF (15 mL), mixed with an equal volume of distilled water and cooled. The white precipitate was collected by filtration, washed with water and dried (yield: 0.12 g); m.p. >310° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242443B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-92da720591f6476c88608fb152406d38 |
| Source note | uspto-grants-2001_06 |