HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809179Generated: November 1, 2026
Chloroacetone → 8-Chloro-2-methylimidazo[1,2-a]pyrazine
https://huagongshe.com/reaction/1809179
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-3-chloropyrazine | HCID 276224 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Chloro-2-methylimidazo[1,2-a]pyrazine | HCID 13389082 | 7.9% |
Reaction Steps
A solution of 2-amino-3-chloropyrazine (10 g, 77.5 mmol), chloroacetone (30 mL, 387 mmol) in MeOH (25 mL) is refluxed overnight at 88° C. It is then stirred for 1 h at 0° C. and any solid that forms, is filtered off and washed twice with MeOH (5 mL). The mother liq. are evaporated, diluted with EtOAc, and washed with HCl 2N, water and brine. The water and HCl mother liq. are evaporated to give a yellow solid that is neutralized with a saturated solution of K2CO3 in water, extracted with DCM, dried with MgSO4 anh. filtered and concentrated. The crude material is purified by column chromatography using a gradient of (DCM/MeOH: 1/0 to 99/1) to give 8-Chloro-2-methyl-imidazo[1,2-a]pyrazine as an orange solid (1.02 g, 7.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362018B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-11bc6c510268416392ca4501d243b67c |
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| Source note | uspto-grants-2013_01 |
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