HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → Imidazo(1,2-b)pyridazine, 6-chloro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Imidazo(1,2-b)pyridazine, 6-chloro- | HCID 138828 | 70.3% |
Reaction Steps
5.0 g (38.6 mmol) of 3-amino-6-chloropyridazine were heated together with 4.7 mL (40 mmol) of chloroacetaldehyde (55% strength in water) in 15 mL of n-butanol at 120° C. for a period of 5 days. After the reaction was complete, the reaction mixture was added to saturated sodium bicarbonate solution and extracted three times with ethyl acetate. The combined organic phases were then washed with brine and dried over sodium sulfate, and the solvent was removed in vacuo. In the final purification by chromatography on silica gel, 4.17 g (70%) of the desired product were isolated in the form of an amorphous white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409889B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-6f1c10914c7e4d20af5db61142bd97e3 |
| Source note | uspto-grants-2016_08 |