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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233860Generated: October 31, 2026

4-(N-Boc-amino)piperidine → HCID 86608254, compound

https://huagongshe.com/reaction/2233860

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantN-[6-Chloro-2-(methylsulfanyl)pyrimidin-4-yl]acetamideHCID 13447564—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86608254HCID 8660825493.8%

Reaction Steps

TEA (0.32 ml, 2.28 mmol) and N-[6-chloro-2-(methylthio)pyrimidin-4-yl]acetamide (Intermediate 44, 0.50 g, 2.28 mmol) were added to a solution of tert-butyl piperidin-4-ylcarbamate (0.46 g, 2.28 mmol) in NMP (2 ml) at room temperature. Using a Smith Microwave Synthesizer, the mixture was subjected to single-mode microwave at 150° C. for 10 minutes. The mixture was partitioned between water and EtOAc. The layers were separated and the organic layer was washed with water two more times. The organic phase was dried over magnesium sulfate and concentrated to give the title compound (816 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-aea0fc5df0d64898b667f0ef62ea0015
Source noteuspto-grants-2010_05