HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067605Generated: October 26, 2026
Water → Isopropyl 6-chloro[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylate
https://huagongshe.com/reaction/1067605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylic acid | HCID 22989292 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Isopropyl 6-chloro[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylate | HCID 22989245 | — |
Reaction Steps
2.14 g of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine-2-carboxylic acid and 5.57 ml of N-ethyldiisopropylamine were dissolved in 30 ml of N,N-dimethylformamide; 3.23 ml of isopropyl iodide was added, followed by stirring at room temperature for 10 hours and at 50° C. for 3 hours. After cooling, water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. The dry product was concentrated under reduced pressure; the residue was subjected to silica gel column chromatography and eluted with ethyl acetate. The desired fraction was collected and concentrated under reduced pressure to yield 2.21 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06248740B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-3658b14e961f444c9585efa4a9a0fe50 |
|---|
| Source note | uspto-grants-2001_06 |
|---|