HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 6-Chloroimidazo[1,2-b]pyridazine-8-carboxylic acid hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Ethyl 6-chloroimidazo[1,2-b]pyridazine-8-carboxylate | HCID 57786728 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Chloroimidazo[1,2-b]pyridazine-8-carboxylic acid hydrazide | HCID 57786668 | 57% |
Reaction Steps
To a solution of crude 6-chloro-imidazo[1,2-b]pyridazine-8-carboxylic acid ethyl ester (5.00 g, “22 mmol”) in 40 mL of ethanol at 0-5° C. was added 10 mL of hydrazine hydrate. Yellow solid immediately precipitated. After 15 min. at 0-5° C., the solid was isolated by Buchner filtration, rinsing well with ice-cold ethanol (250 mL total) and dried by sucking air through then in vacuo. A small amount of additional solid precipated from the filtrate and was isolated and dried similarly to the first crop. A total of 2.38 g (57% over three steps) of 6-chloro-imidazo[1,2-b]pyridazine-8-carboxylic acid hydrazide was isolated as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426441B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-7768b1badc6d42ada02d6eae700bea02 |
| Source note | uspto-grants-2013_04 |