HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 5-Bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carbohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Ethyl 5-bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylate | HCID 117727933 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carbohydrazide | HCID 117727835 | — |
Reaction Steps
A mixture of compound 21a (1.6 g, 4.5 mmol) and hydrazine monohydrate (2.6 mL, 27 mmol) in EtOH (20 mL) was heated at reflux overnight. An off-white solid formed, the collected by filtration and dried under reduced pressure to give 5-bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carbohydrazide which was directly used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249163B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-e3ae25c557e94989810abc76a750e79b |
| Source note | uspto-grants-2016_02 |