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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550823Generated: October 31, 2026

4-(N-Boc-amino)piperidine → [1-(7-Methoxy-thiazolo[5,4-d]pyrimidin-2-ylcarbamoyl)-piperidin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/550823

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant(7-Methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-carbamic acid phenyl esterHCID 59011944—
SolventAcetonitrileHCID 6342—
Product[1-(7-Methoxy-thiazolo[5,4-d]pyrimidin-2-ylcarbamoyl)-piperidin-4-yl]-carbamic acid tert-butyl esterHCID 5901196390.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-carbamic acid phenyl ester (6 g, 19.8 mmol) and piperidin-4-yl-carbamic acid tert-butyl ester (4.37 g, 21.8 mmol) in acetonitrile (400 mL) was heated to reflux for 1 h and was then stirred at 25° C. overnight. The resulting solid was collected by filtration, rinsed with acetonitrile and dried in vacuo to afford [1-(7-methoxy-thiazolo[5,4-d]pyrimidin-2-ylcarbamoyl)-piperidin-4-yl]-carbamic acid tert-butyl ester (7.3 g, 90%) as a white solid; ES-HRMS m/e calcd for C17H24N6O4S (M+H)+ 409.1653, found 409.1653.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947692B2
Source datasetuspto-grants-2011_05
ORD IDord-765818d252354ee89b17c56cc537cafb
Source noteuspto-grants-2011_05