HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70201Generated: October 28, 2026
Ammonium formate → Tert-butyl 2-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/70201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-Tert-butyl 4-benzyl 2-((pyridin-3-yloxy)methyl)piperazine-1,4-dicarboxylate | HCID 59671606 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 2-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate | HCID 59671473 | 87.1% |
Reaction Steps
Palladium hydroxide on carbon (˜40% palladium, 0.170 g, 0.12 mmol) was added to a solution of 1-tert-butyl 4-benzyl 2-((pyridin-3-yloxy)methyl)piperazine-1,4-dicarboxylate (0.649 g, 1.52 mmol) and ammonium formate (0.191 g, 3.03 mmol) in EtOH (10 mL), and the reaction mixture was heated to 80° C. for 2 h. Upon cooling to rt, the reaction mixture was diluted with EtOAc (40 mL) and washed with water (3×30 mL) and brine (30 mL). The organics were dried over Na2SO4, filtered, and concentrated under reduced pressure, yielding 388.4 mg (87%) of the desired product as a white, waxy solid. LC-MS: RT=3.90 min, [M+H]+=294.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822472B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-68f5d6a81e6b46de9ec8733c8f0b32b4 |
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| Source note | uspto-grants-2014_09 |
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