HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminopyrazine → (2S,4S)-Benzyl 4-methoxy-2-(pyrazin-2-ylcarbamoyl)pyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | (2S,4S)-1-Benzyl 2-methyl 4-methoxypyrrolidine-1,2-dicarboxylate | HCID 14036172 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,4S)-Benzyl 4-methoxy-2-(pyrazin-2-ylcarbamoyl)pyrrolidine-1-carboxylate | HCID 59436412 | 85.1% |
Reaction Steps
To a solution of aminopyrazine (535 mg, 5.63 mmol) in THF (15 mL) was added isopropylmagnesium chloride (2.0 M THF solution, 2.7 mL, 5.35 mmol) dropwise at 0° C. The resulting slurry was stirred at room temperature for 30 min. A solution of (2S,4S)-1-benzyl 2-methyl 4-methoxypyrrolidine-1,2-dicarboxylate (550 mg, 1.88 mmol) in THF (2 mL) was added to the slurry. The reaction mixture was stirred at room temperature for 4 h and quenched with methanol (3 mL). The crude product was purified by preparative HPLC to give (2S,4S)-benzyl 4-methoxy-2-(pyrazin-2-ylcarbamoyl)pyrrolidine-1-carboxylate 18C (570 mg, 85%) as an oil. LC/MS [M+H]+: 356; Ret time (Method F): 2.32 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415340B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-7ec2fd0e773d4157a70ca75a200d8778 |
| Source note | uspto-grants-2013_04 |