HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 5-(Pyrrolidin-1-yl)pyrazin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 2-Amino-5-bromopyrazine | HCID 599539 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(Pyrrolidin-1-yl)pyrazin-2-amine | HCID 25094154 | 43.7% |
Reaction Steps
A mixture of 5-bromopyrazin-2-amine (1.2 g, 6.9 mmol) and pyrrolidine (4 mL, 48 mmol) was microwaved at 180° C., 200 W for 2 h. The reaction was diluted into 125 mL ethyl acetate and extracted with water (3×50 mL) and brine (50 mL). It was dried over sodium sulfate, filtered and concentrated. The crude product was purified by column chromatography (0 to 3% methanol/methylene chloride) to afford 5-(pyrrolidin-1-yl)pyrazin-2-amine (495 mg, 3. mmol, 43.7% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.52 (1 H, d, J=1.51 Hz), 7.36 (1 H, d, J=1.76 Hz), 5.21 (2H, s), 3.24-3.29 (4 H, m), 1.90 (4 H, ddd, J=6.48, 3.53, 3.34 Hz). MS (LC/MS) R.T.=0.52; [M+H]+=165.29.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863291B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-803fcb26aa49481396b3b1791be9648f |
| Source note | uspto-grants-2011_01 |