Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643348Generated: October 30, 2026

Methyl iodide → 3-[(S)4-Boc-3-benzylpiperazinyl]-5-bromo-2-methylaminopyrazine

https://huagongshe.com/reaction/643348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-amino-5-bromo-3-[(S)-4-Boc-3-benzylpiperazinyl]pyrazineHCID 59262247—
Solvent1,4-DioxaneHCID 31275—
Product3-[(S)4-Boc-3-benzylpiperazinyl]-5-bromo-2-methylaminopyrazineHCID 59262259309.9%

Reaction Steps

To a solution of 2-amino-5-bromo-3-[(S)4-Boc-3-benzylpiperazinyl]pyrazine 108 (140 mg, 0.313 mmol) in anhydrous dioxane (3 mL) was added a 1 M solution of potassium t-butoxide (0.34 mL, 0.34 mmol). The reaction mixture was stirred at room temperature for 10 minutes and iodomethane (89 mg, 0.627 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours. Ethyl acetate (100 mL) was added. The organic layer was washed with water and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporated under reduced pressure. The crude product was purified by RP-HPLC to yield the desired 3-[(S)-4-Boc-3-benzylpiperazinyl]-5-bromo-2-methylaminopyrazine 111 (45 mg, 0.97 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700601B2
Source datasetuspto-grants-2010_04
ORD IDord-cc81edb18aba4267b8396430a206b9dc
Source noteuspto-grants-2010_04