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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264433Generated: October 30, 2026

4-Amino-1-Boc-piperidine → HCID 68781993, compound

https://huagongshe.com/reaction/2264433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant4-Amino-2-chloropyrimidine-5-carbonitrileHCID 2801166—
SolventDimethylformamideHCID 6228—
ProductHCID 68781993HCID 68781993—

Reaction Steps

A mixture of 4-amino-2-chloro-pyrimidine-5-carbonitrile (2.0 g, 12.94 mmol, 1.0 equiv; commercially available) and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (3.1 g, 15.53 mmol, 1.2 equiv; commercially available) in anhydrous DMF (20 mL) was heated to 60° C. for 4 h. The organic phase was concentrated under reduced pressure and the crude product purified by crystallization from ethyl acetate providing 3.02 g (74%) of the title compound. MS (ISN): 317.1 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855194B2
Source datasetuspto-grants-2010_12
ORD IDord-06fbf30802a94f7ba497fe3657dd76ba
Source noteuspto-grants-2010_12