HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450552Generated: October 25, 2026
Formic Acid → 2-(tetrahydro-2H-pyran-4-yloxy)pyridin-3-amine
https://huagongshe.com/reaction/450552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 3-Nitro-2-(tetrahydro-2H-pyran-4-yloxy)pyridine | HCID 53256715 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(tetrahydro-2H-pyran-4-yloxy)pyridin-3-amine | HCID 53256608 | — |
Reaction Steps
To a solution of 3-nitro-2-(tetrahydro-2H-pyran-4-yloxy)pyridine (2.31 g, 10.3 mmol) in anhydrous MeOH (20 mL) was added ammonium formate (1.2 g, 19.1 mmol) and palladium hydroxide on carbon (20%, 0.40 g). The mixture was stirred at ambient temperature for 8 hours when an additional aliquot of ammonium formate (1.0 g) was added. The mixture was heated at 50° C. for 4 hours, the solution adjusted to pH 8 with formic acid before further heating at 50° C. for one hour. The reaction was filtered through Celite and the catalyst residue washed with MeOH. The solvent was concentrated in vacuo to give a deep purple solid. The crude product was purified by ion-exchange chromatography (SCX-2 eluting with hydrochloric acid/MeOH ammonia/MeOH). The product crystallised as a white solid (1.8 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486953B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ae76f51eb7ce4f72944d1c3547d07d08 |
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| Source note | uspto-grants-2013_07 |
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