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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047230Generated: November 2, 2026

Ethanol → HCID 86664798, compound

https://huagongshe.com/reaction/2047230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonium formateHCID 2723923—
ReactantHCID 86664797HCID 86664797—
CatalystPalladium hydroxideHCID 9942167—
ProductHCID 86664798HCID 86664798—

Reaction Steps

This material, tert-butyl (1-benzylpiperidin-4-yl)methyl(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(6-fluoroquinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl)carbamate, was then stirred with Pd(OH)2/C (0.2 equiv) and ammonium formate (20 equiv) in ethanol at 80° C. until the reaction was deemed complete by HPLC, LC-MS, or TLC analysis. The mixture was allowed to cool to room temperature, filtered through a pad of celite, concentrated and purified on silica gel to afford compound tea-butyl 7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(6-fluoroquinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl(piperidin-4-ylmethyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591943B2
Source datasetuspto-grants-2013_11
ORD IDord-b627ed6af6864384a0c9cccb9e09f7bd
Source noteuspto-grants-2013_11