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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005875Generated: October 27, 2026

4-Cyanophenylboronic acid → 4-[5-(4-Cyanophenyl)pyrimidin-2-yl]piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1005875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanophenylboronic acidHCID 2734326—
Reactanttert-Butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylateHCID 21914476—
ReactantTert-butyl 4-[5-(4-fluorophenyl)pyrimidin-2-yl]piperazine-1-carboxylateHCID 69850026—
Product4-[5-(4-Cyanophenyl)pyrimidin-2-yl]piperazine-1-carboxylic acid tert-butyl esterHCID 6989408368%

Reaction Steps

Prepared according to the method for the preparation of 4-[5-(4-fluorophenyl)pyrimidin-2-yl]piperazine-1-carboxylic acid tert-butyl ester, from 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (1.00 g) and 4-cyanobenzeneboronic acid (0.47 g), to yield the title compound as a white solid (0.72 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787536B2
Source datasetuspto-grants-2004_09
ORD IDord-ed5b3619193542e89849081663de63d1
Source noteuspto-grants-2004_09