HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742008Generated: October 29, 2026
HCID 19429288, compound → HCID 19429294, compound
https://huagongshe.com/reaction/1742008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19429288 | HCID 19429288 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19429294 | HCID 19429294 | 98% |
Reaction Steps
Ethyl 1-methyl-5,6-dihydroimidazo[1,5-a]pyridine-7-carboxylate (0.90 g) was subjected to catalytic reduction in 30 ml methanol at room temperature for ten hours by using 0.02 g of 5% paradium-carbon as the catalyst. The reaction mixture was filtered, the filtrate was concentrated to dryness under reduced pressure, ethyl acetate was added to the residue, and the resulting mixture was extracted with 0.5N-HCl. The aqueous layer collected was alkalized by addition of potassium carbonate and then extracted with dichloromethane, the organic layer collected was washed with saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure, thus giving 0.89 g (98 %) of ethyl 1-methyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine-7-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05336679 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-b35a5af848d14a2d85c8a10c20d39b50 |
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| Source note | uspto-grants-1994_08 |
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