Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910666Generated: October 29, 2026

Potassium Fluoride → 4-(4-Chloro-6-thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/910666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantThiophene-3-boronic acidHCID 581760—
ReactantHCID 11045887HCID 11045887—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
Product4-(4-Chloro-6-thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 86628634—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-(4,6-dichloro-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester (167.1 mg, 0.5 mmol) in anhydrous 1,4-dioxane (4 mL) in an oven-dried flask was added 3-thiopheneboronic acid (70.4 mg, 0.55 mmol), Pd[P(t-Bu)3]2 (2.5 mg, 0.005 mmol), tris(dibenzylideneacetone)-dipalladium(0) (2.3 mg, 0.0025 mmol), and KF (64 mg, 1.1 mmol). The resulting mixture was vacuum flushed with argon and heated overnight at 90° C. The reaction mixture was cooled and passed through a pad of diatomaceous earth, washing with EtOAc. The filtrate was concentrated and the residue was purified by preparative TLC (EtOAc/hexanes, 1:4) to yield a white solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022209B2
Source datasetuspto-grants-2011_09
ORD IDord-6739acb440234ef59eba849505fe86db
Source noteuspto-grants-2011_09