HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Chloro-2-methylimidazo(1,2-b)pyridazine | HCID 10442072 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine | HCID 13712154 | 90% |
Reaction Steps
To a solution of 6-chloro-2-methylimidazo[1,2-b]pyridazine (2.00 g, 11.9 mmol, 1.0 equiv) in chloroform (50 mL) was added N-bromosuccinimide (2.55 g, 14.3 mmol, 1.2 equiv). The reaction was stirred at room temperature for 15 h. Purification by column chromatography using 50% ethyl acetate in hexanes elution gave 2.64 g of the yellow solid, 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09370515B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-640d062234ad42fa8b9b04a620e06e43 |
| Source note | uspto-grants-2016_06 |