HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809193Generated: November 1, 2026
Imidazole → 8-Hydroxy-6-methylimidazo[1,2-a]pyrazine
https://huagongshe.com/reaction/1809193
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | 1,6-Dimethyl-8-oxo-7,8-dihydro-imidazo[1,2-a]pyrazin-1-ium bromide salt | HCID 86655089 | — |
| Product | 8-Hydroxy-6-methylimidazo[1,2-a]pyrazine | HCID 45788522 | 39.7% |
Reaction Steps
A mixture of 1,6-dimethyl-8-oxo-7,8-dihydro-imidazo[1,2-a]pyrazin-1-ium bromide salt (4.3 g, 16.4 mmol) and imidazole (20.4 g, 310 mmol) is stirred at 175° C. for 20 h. After this time the reaction mixture is cooled down to 100° C. and poured into ice-water with vigorous stirring. No precipitation is observed therefore the solvent is removed and the imidazole distilled off under vacuum at approx. 130° C. The solid remaining is triturated with DCM to give 6-methyl-7H-imidazo[1,2-a]pyrazin-8-one as a brown solid (970 mg). The mother liq. are purified by column chromatography using a gradient of (DMC/MeOH:99/1 to 95/5) to give a further 667 mg of 6-methyl-7H-imidazo[1,2-a]pyrazin-8-one as a pale yellow solid (1.66 g, 68%).
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-2250f6869a814f4cb9ec6237b95b2f5c |
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| Source note | uspto-grants-2013_01 |
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