HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57875Generated: October 29, 2026
tert-butyl 4-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3,6-dihydro-2H-pyridine-1-carboxylate → Tert-butyl 4-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]piperidine-1-carboxylate
https://huagongshe.com/reaction/57875
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl 4-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3,6-dihydro-2H-pyridine-1-carboxylate | HCID 86707059 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butyl 4-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]piperidine-1-carboxylate | HCID 86707071 | — |
Reaction Steps
A mixture of tert-butyl 4-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3,6-dihydro-2H-pyridine-1-carboxylate (125 mg, 0.266 mmol) and palladium on activated carbon, reduced 10% (28 mg, 0.0266 mmol) in ethanol 10.0 mL was stirred under H2 balloon at 40° C. 18 h. The reaction was filtered through celite and wash with MeOH. The crude product was carried to next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434725B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-006e66199ade4683bfde18aa539ff568 |
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| Source note | uspto-grants-2016_09 |
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