HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-[(S)4-Boc-3-benzylpiperazinyl]-5-bromo-2-methylaminopyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-amino-5-bromo-3-[(S)-4-Boc-3-benzylpiperazinyl]pyrazine | HCID 59262247 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-[(S)4-Boc-3-benzylpiperazinyl]-5-bromo-2-methylaminopyrazine | HCID 59262259 | 309.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700601B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-cc81edb18aba4267b8396430a206b9dc |
| Source note | uspto-grants-2010_04 |