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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | N-(3-bromo-4-methoxyphenyl)acetamide | HCID 244158 | — |
| Reagent | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Palladium (II) acetate | HCID 4144353 | — |
| Catalyst | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl | HCID 16217985 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-methoxy-3-piperazin-1-yl-phenyl)-acetamide | HCID 82480614 | 50.91% |
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 dataset | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-d3fce1c8e3204b57a80e5c0d53c5c1f7 |
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| Source note | 750 AstraZeneca ELN dataset |
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