HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazine → 3-Methyl-2-{[(7-methyl[1,2,4]triazolo[1,5-b]pyridazin-6-yl)oxy]methyl}butane-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazine | HCID 11805158 | — |
| Reactant | HCID 53813453 | HCID 53813453 | — |
| Product | 3-Methyl-2-{[(7-methyl[1,2,4]triazolo[1,5-b]pyridazin-6-yl)oxy]methyl}butane-1-sulfonamide | HCID 3073795 | — |
Reaction Steps
Using 3-(N,N-dimethylaminomethylene)aminosulfonyl-2-isopropyl-1-propanol and 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction as in Example 6 was conducted to produce the title compound. m.p. 196°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389633 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-f2f08a6109a7481297eb97a18b836d0e |
| Source note | uspto-grants-1995_02 |