HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 3-(4-Methylpiperazin-1-yl)-5-nitropyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 4-Amino-3-bromo-5-nitropyridine | HCID 4997588 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | 3-(4-Methylpiperazin-1-yl)-5-nitropyridin-4-amine | HCID 86698329 | 56.9% |
Reaction Steps
A solution of 3-bromo-5-nitropyridin-4-amine (LXIX) (618 mg, 2.83 mmol) in 1-methylpiperazine (1 mL, 8.51 mmol) was heated at 140° C. overnight. The reaction was poured into an EtOAc/H2O mixture; the organic layer was separated, dried over MgSO4 and concentrated under vacuum. The crude product was purified on a silica gel column (100% CHCl3→3:97 MeOH(7N NH3):CHCl3) to give 3-(4-methylpiperazin-1-yl)-5-nitropyridin-4-amine (CXVII) as a yellow solid (382 mg, 1.61 mmol, 56.7% yield). 1H NMR (CDCl3, 500 MHz,) δ ppm 2.20 (s, 3H), 2.35-2.37 (m, 4H), 4.52-3.54 (m, 4H), 5.96 (s, 1H), 7.42 (s, 2H), 8.78 (s, 1H); ESIMS found C10H15N5O2 m/z 238 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883822B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-269ee2d65bcd404580bab2baea26fac4 |
| Source note | uspto-grants-2014_11 |