HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059347Generated: October 31, 2026
1-Benzyl-4-piperidylamine → HCID 178505158, compound
https://huagongshe.com/reaction/1059347
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | Ethyl (methanesulfonyl)methanimidate | HCID 54392285 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178505158 | HCID 178505158 | 39.3% |
Reaction Steps
Into a solution of 760 mg of ethyl N-methanesulfonyl-formimidate in diethyl ether (20 ml) was dropped 0.95 g of 4-amino-1-benzylpiperidine at room temperature. After stirring for 2 hours, the crystals thus precipitated were filtered and washed with diethyl ether to thereby give 580 mg of N2-methanesulfonyl-N1-(1-benzylpiperidin-4-yl)formamidine as colorless needles. These crystals were dissolved in 30 ml of methanol and 500 mg of 10% palladium-carbon was added thereto. Then the resulting mixture was stirred in a hydrogen atmosphere under atmospheric pressure for 1 hour followed by filtration through celite. After distilling off the solvent under reduced pressure, the residue was recrystallized from acetone/ethyl acetate to thereby give 310 mg of the title compound as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518423B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-1b8f01b7c619488cbeede27e00cb2a58 |
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| Source note | uspto-grants-2003_02 |
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