HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182150Generated: November 3, 2026
tert-Butyl piperazine-1-carboxylate → 1-Boc-4-(3-amino-6-bromopyrazin-2-YL)piperazine
https://huagongshe.com/reaction/2182150
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Boc-4-(3-amino-6-bromopyrazin-2-YL)piperazine | HCID 46864072 | — |
Reaction Steps
2-Amino-3,5-dibromopyrazine (1.26 g, 5.0 mmol) and piperazine-1-carboxylic acid tert-butyl ester (4.64 g, 25 mmol) were placed in a dry RBF and heated with stirring to 120° C. under dry nitrogen. Molten mixture was stirred at this temperature for 6 h and cooled to room temperature. The resulting slurry was diluted with EtOAc (20 mL) and stirred for 20 min. Amine salts were removed by filtration and washed with EtOAc (3×5 mL). Filtrate was washed with pH 4 buffer (35 mL) and brine (35 mL), dried over Na2SO4 (anhydrous), filtered, and concentrated in vacuo. The residue was purified by flash chromatography (hexanes/EtOAc 7:3) gives the title compound I-3r as an off white solid (1.64 g, 92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06894050B2 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-d70f6060e70648bca8937a602e994a9d |
|---|
| Source note | uspto-grants-2005_05 |
|---|