HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920954Generated: October 31, 2026
Chloroacetaldehyde → Imidazo(1,2-a)pyrazine
https://huagongshe.com/reaction/920954
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | Imidazo(1,2-a)pyrazine | HCID 2771670 | 50% |
Reaction Steps
Pyrazin-2-amine 4a (5 g, 52 mmol) was dissolved in a 40% 2-chloroacetaldehyde solution (15 mL, 78 mmol), followed by addition of sodium bicarbonate (6.60 g, 78 mmol). After stirring for 48 hours at 100° C., the reaction mixture was cooled to room temperature, added with 100 mL of a saturated potassium carbonate solution, and extracted with dichloromethane (100 mL×3). The organic phase was combined, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to obtain imidazo[1,2-a]pyrazine 4b (3 g, yield 50.0%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273052B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-18e409b58c634ae8986b858380f617b3 |
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| Source note | uspto-grants-2016_03 |
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