HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288739Generated: October 29, 2026
Ammonium formate → 1-[1-(4-Pyrimidinyl)-4-piperidylcarbonyl]piperazine
https://huagongshe.com/reaction/2288739
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-Benzyl-4-[(1-[4-pyrimidinyl]-4-piperidyl)carbonyl]piperazine | HCID 18698066 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[1-(4-Pyrimidinyl)-4-piperidylcarbonyl]piperazine | HCID 18697970 | 94.3% |
Reaction Steps
Ammonium formate (1.88 g) was added to a mixture of 1-benzyl-4-[(1-[4-pyrimidinyl]-4-piperidyl)carbonyl]piperazine (2.73 g) and 10% palladium on carbon catalyst (0.55 g) in methanol (70 ml) under an atmosphere of argon. The mixture was stirred at reflux temperature for 1 hour. The cooled mixture was filtered through diatomaceous earth and the filtercake was well washed with methanol. The filtrate and washings were combined and evaporated. The residual oil was suspended in saturated aqueous sodium carbonate solution (30 ml) and the mixture was extracted with dichloromethane (4×100 ml). The dichloromethane extracts were combined, dried (Na2SO4) and evaporated to give 1-[(1-[4-pyrimidinyl]-4-piperidyl)carbonyl]piperazine (1.94 g, 94%) as an off-white solid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090813 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-eeb5311c887a409cb52ce77523097ce7 |
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| Source note | uspto-grants-2000_07 |
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