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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772641Generated: November 1, 2026

2-Chloropyrimidine → tert-Butyl 4-(5-(8-morpholino-2-((pyrimidin-2-yloxy)methyl)imidazo[1,2-a]pyrazin-5-yl)pyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1772641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
Reactanttert-Butyl 4-(5-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-a]pyrazin-5-yl)pyridin-2-yl)piperazine-1-carboxylateHCID 117733761—
Producttert-Butyl 4-(5-(8-morpholino-2-((pyrimidin-2-yloxy)methyl)imidazo[1,2-a]pyrazin-5-yl)pyridin-2-yl)piperazine-1-carboxylateHCID 131734674—

Reaction Steps

Following the procedures described in Example 22, Step A, the title compound was prepared from compound 23a and 2-chloropyrimidine. Mass Spectrum (LCMS, ESI pos.) Calcd. for C29H35N9O4: 574.3 (M+H). Found 574.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249163B2
Source datasetuspto-grants-2016_02
ORD IDord-fd0761f1a6a14035b15cb8488ddc635e
Source noteuspto-grants-2016_02