Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 68642024 | HCID 68642024 | — |
| Product | HCID 68641311 | HCID 68641311 | 84% |
Reaction Steps
In ethanol (200 ml), 1,2,3,4-tetrahydrobenzo[4,5]imidazo[1,2-a]pyrazine-8-carboxylic acid (2.94 g, 13.53 mmol) prepared in the Step 38-1-4 was suspended. Concentrated sulfuric acid (10 ml) was added thereto, and the mixture was heated under reflux for 72 hours. After being allowed to cool, the mixture was concentrated under a reduced pressure. The concentrate was neutralized with a saturated sodium bicarbonate solution and 25% ammonia water and then subjected to extraction with chloroform. The extract was dried over anhydrous magnesium sulfate and then concentrated under a reduced pressure. The concentrate was purified by silica gel column chromatography (chloroform:methanol=10:1) to give the title compound (2.78 g, 84%) as a light-yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200008B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-1af817bebd764d598701fea8ca2599d3 |
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| Source note | uspto-grants-2015_12 |
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