HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 8-Chloro-6-methyl-imidazo[1,2-a]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 8-Hydroxy-6-methylimidazo[1,2-a]pyrazine | HCID 45788522 | — |
| Product | 8-Chloro-6-methyl-imidazo[1,2-a]pyrazine | HCID 10374814 | 35% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
Pyridine (0.4 mL, 4.9 mmol) was added to a solution of 6-methyl-7H-imidazo[1,2-a]pyrazin-8-one (0.97 g, 6.5 mmol) in POCl3 (19 mL) and the reaction is stirred at 120° C. under N2 atmosphere for 4 h 30 min. The reaction is cooled to 60° C. and poured into 60 g of ice and stirred for 1 h. The solution is neutralized with NaOH (10%), extracted with CHCl3/IPA 9/1, dried with MgSO4 anh., filtered and concentrated. The crude product is purified by column chromatography using a gradient of (DCM/MeOH:99/1 to 95/5) to give 8-chloro-6-methyl-imidazo[1,2-a]pyrazine as a pale yellow solid (0.383 g, 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362018B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-f08c52e6859e49248d2d83f57aac179f |
| Source note | uspto-grants-2013_01 |