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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40746Generated: October 29, 2026

2,4-Dichloropyrimidine → 3-(2-Chloropyrimidin-4-yl)-5-morpholinobenzonitrile

https://huagongshe.com/reaction/40746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant3-Bromo-5-morpholinobenzonitrileHCID 44627367—
Reactant3-Morpholino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 44627474—
Product3-(2-Chloropyrimidin-4-yl)-5-morpholinobenzonitrileHCID 44627480—

Reaction Steps

3-(2-Chloropyrimidin-4-yl)-5-morpholinobenzonitrile was prepared according procedure B from 2,4-dichloropyrimidine and 3-morpholino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile which was synthesized by following procedure A using 3-bromo-5-morpholinobenzonitrile and bis(pinacolato)diboron.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530480B2
Source datasetuspto-grants-2013_09
ORD IDord-1fada1ee4a4c49a3ba33ad6894d2f7aa
Source noteuspto-grants-2013_09