Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448Generated: October 27, 2026

tert-Butyl piperazine-1-carboxylate → tert-Butyl4-[5-(trifluoromethyl)pyridin-3-yl]piperazine-1-carboxylate

https://huagongshe.com/reaction/448

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
ReagentSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl4-[5-(trifluoromethyl)pyridin-3-yl]piperazine-1-carboxylateHCID 5983355585.94%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 100 ml round bottom equipped with stir bar was charged with (S)-BINAP (331 mg, 0.53 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (203 mg, 0.22 mmol) dissolved in 1,4-dioxane (10.700 mL). This was degassed and purged with nitrogen and stirred at RT for 10 mins. 3-bromo-5-(trifluoromethyl)pyridine (500 mg, 2.21 mmol) followed by tert-butyl piperazine-1-carboxylate (824 mg, 4.42 mmol) and sodium tert-butoxide (850 mg, 8.85 mmol) were added, and the reaction was stirred at 80 °C for 2 hrs. The crude material was loaded on a Snap KP-SIL 100g column and purified on a Biotage Isolera One instrument, eluting with 10% to 30% ethyl acetate in heptane to provide tert-butyl 4-(5-(trifluoromethyl)pyridin-3-yl)piperazine-1-carboxylate (630 mg, 86 %) as an oil.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-9b1d1f242a294d85b376889807570e77
Source note750 AstraZeneca ELN dataset