HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide → 1-Pentanesulfonamide, 4,4-dimethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide | HCID 10726520 | — |
| Reactant | 6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazine | HCID 11805158 | — |
| Product | 1-Pentanesulfonamide, 4,4-dimethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)- | HCID 3073788 | — |
Reaction Steps
Using 5-hydroxy-4,4-dimethyl-1-pentanesulfonamide and 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction was conducted as in Example 5 to produce the title compound. m.p. 171°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389633 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-55d85fa45f36489eabca2860c9c974a7 |
| Source note | uspto-grants-1995_02 |