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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589154Generated: November 1, 2026

Tert-butyl 3-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylate → Tert-butyl 3-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate

https://huagongshe.com/reaction/589154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylateHCID 66584641—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 3-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-8-azabicyclo[3.2.1]octane-8-carboxylateHCID 66584984—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of tert-butyl 3-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-8-azabicyclo[3.2.1]oct-3-ene-8-carboxylate (12.2 g, 20.3 mmol) and 10% Pd/C (2.1 g) in EtOAc (175 ml) was stirred at 45° C. under hydrogen (balloon pressure) for 16 hours. After filtration and concentration, the crude mixture of two isomers was purified by gradient column chromatography on silica eluting with EtOAc/Hexanes (0-35%) to give the slightly impure “endo” product (6.24 g, Rf=0.6 in 25% EtOAc/Hexanes) and the “exo” product (5.44 g, Rf=0.5 in 25% EtOAc/Hexanes) which was used in the following reaction sequences.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227971B2
Source datasetuspto-grants-2016_01
ORD IDord-16152f16464e4edd9b95fd161d6befc8
Source noteuspto-grants-2016_01