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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | HCID 11045887 | HCID 11045887 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(4-Chloro-6-thiophen-3-yl-[1,3,5]triazin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 86628634 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08022209B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-6739acb440234ef59eba849505fe86db |
|---|
| Source note | uspto-grants-2011_09 |
|---|