HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21913932, compound → HCID 21913266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21913932 | HCID 21913932 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21913266 | HCID 21913266 | 85% |
Reaction Steps
Under a nitrogen atmosphere, 1,8-diazabicyclo[5.4.0]undecene-7 (4.2 mL, 28 mmol) was added to a solution of 3-chloro-N-{2-[2-(8-ethyl-5,6-dimethyl-7H-imidazo[4,5-c]tetrazolo[1,5-a]pyridin-7-yl)ethoxy]ethyl}propane-1-sulfonamide (2.50 g, 5.63 mmol) in DMF (50 mL), and the reaction was stirred overnight at room temperature. The solution was concentrated to about 25 mL under reduced pressure, and water (300 mL) was added. A white precipitate formed, which was isolated by filtration and recrystallized from acetonitrile (20 mL) to provide 1.95 g of 7-{2-[2-(1,1-dioxidoisothiazolidin-2-yl)ethoxy]ethyl}-8-ethyl-5,6-dimethyl-7H-imidazo[4,5-c]tetraazolo[1,5-a]pyridine as white crystals, m. p. 176–178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125890B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-dc0aaf515c1346dcaa597143b8bbade1 |
| Source note | uspto-grants-2006_10 |