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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725762Generated: October 29, 2026

Ethyl 4-amino-1-piperidinecarboxylate → HCID 69055408, compound

https://huagongshe.com/reaction/1725762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantN'-((Dimethylamino)methylene)-N,N-dimethylformohydrazonamideHCID 9613942—
SolventTolueneHCID 1140—
ProductHCID 69055408HCID 6905540875.3%

Reaction Steps

To a stirred solution of ethyl-4-amino-piperidine carboxylate (5 g, 29 mmol) in toluene (100 mL) was added N,N-dimethylformamide azine (8.2 g) and catalytic amount of p-tolunesulfonic acid (0.3 g) and the resulting mixture was refluxed overnight. The mixture was cooled and washed with water, and the aqueous layer was evaporated and the residue was treated with dichloromethane (100 mL). The organic layer was dried over MgSO4, filtered and evaporated. The residue was purified on silica flash column eluting with 4% MeOH, 0.5% NH4OH in dichloromethane to give the desired ethyl 4-(4H-1,2,4-triazol-4-yl)piperidine-1-carboxylate (4.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491737B2
Source datasetuspto-grants-2009_02
ORD IDord-ca61494551de4c0ba48a86ba5066b8dc
Source noteuspto-grants-2009_02