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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928694Generated: October 30, 2026

tert-butyl N-((tert-butoxy)carbonyl)-N-(6-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-yl)carbamate → tert-butyl (6-(6-(bis(tert-butoxycarbonyl)amino)pyrazin-2-yl)imidazo[1,2-a]pyrazin-8-yl)(4-(4-(oxetan-3-yl)piperazin-1-yl)-3-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)carbamate

https://huagongshe.com/reaction/928694

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-((tert-butoxy)carbonyl)-N-(6-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-yl)carbamateHCID 68266589—
Reactanttert-butyl (6-bromoimidazo[1,2-a]pyrazin-8-yl)(4-(4-(oxetan-3-yl)piperazin-1-yl)-3-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)carbamateHCID 118187918—
Producttert-butyl (6-(6-(bis(tert-butoxycarbonyl)amino)pyrazin-2-yl)imidazo[1,2-a]pyrazin-8-yl)(4-(4-(oxetan-3-yl)piperazin-1-yl)-3-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)carbamateHCID 118187923—

Reaction Steps

tert-Butyl (6-bromoimidazo[1,2-a]pyrazin-8-yl)(4-(4-(oxetan-3-yl)piperazin-1-yl)-3-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)carbamate XXVI was reacted with XV according to the methods of CHEMISTRY B as described in Example 2 to provide the desired compound tert-butyl (6-(6-(bis(tert-butoxycarbonyl)amino)pyrazin-2-yl)imidazo[1,2-a]pyrazin-8-yl)(4-(4-(oxetan-3-yl)piperazin-1-yl)-3-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethoxy)phenyl)carbamate XXVII.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290505B2
Source datasetuspto-grants-2016_03
ORD IDord-89100ad3e3294c7691a12896d908083e
Source noteuspto-grants-2016_03