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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521Generated: October 23, 2026

tert-Butyl piperazine-1-carboxylate → N-(4-methoxy-3-piperazin-1-yl-phenyl)-acetamide

https://huagongshe.com/en/reaction/521

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantN-(3-bromo-4-methoxyphenyl)acetamideHCID 244158—
ReagentSodium t-butoxideHCID 23676156—
CatalystPalladium (II) acetateHCID 4144353—
Catalyst2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
SolventTolueneHCID 1140—
ProductN-(4-methoxy-3-piperazin-1-yl-phenyl)-acetamideHCID 8248061450.91%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of N-(3-bromo-4-methoxyphenyl)acetamide (0.5 g, 2.05 mmol) dissolved in toluene (5 mL) was treated with tert-butyl piperazine-1-carboxylate (0.382 g, 2.05 mmol), diacetoxypalladium (0.046 g, 0.20 mmol), dicyclohexyl(2',6'-diisopropoxybiphenyl-2-yl)phosphine (0.191 g, 0.41 mmol) and sodium 2-methylpropan-2-olate (0.433 g, 4.51 mmol) in a sealed tube. The resulting mixture was degassed and stirred at 100 °C for 8 hours in a microwave. The mixture was pre-absorbed onto silica. The crude product was purified by flash silica chromatography, elution 50% ethyl acetate in Heptane. Pure fractions were evaporated to dryness to afford intermediate. The intermediate was dissolved in 4M HCl in dioxane (10mL) and stirred at RT overnight. The mixture was evaporated to give N-(4-methoxy-3-(piperazin-1-yl)phenyl)acetamide (0.260 g, 50.9 %) as a tan solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-d3fce1c8e3204b57a80e5c0d53c5c1f7
Source note750 AstraZeneca ELN dataset