HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 2-(4-methylpiperazin-1-yl)-N-(prop-2-yn-1-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-bromo-N-(prop-2-yn-1-yl)acetamide | HCID 11159617 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-methylpiperazin-1-yl)-N-(prop-2-yn-1-yl)acetamide | HCID 78912508 | 49% |
Reaction Steps
To a solution of 2-bromo-N-(prop-2-yn-1-yl)acetamide (0.7 g, 3.98 mmol) in DCM (10 mL) added N-methyl piperazine (0.66 mL, 5.96 mmol) drop wise. Reaction mixture stirred at rt for 16 h, diluted with DCM and washed with water and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude residue was triturated with ether-pentane, affording the title compound (0.38 g, 49%); LCMS: m/z=196.15 (M+1); 1H NMR (300 MHz, DMSO-d6) δ 8.06 (d, J=6.1 Hz, 1H), 3.86 (dd, J=5.9, 2.5 Hz, 2H), 3.07 (t, J=2.5 Hz, 1H), 2.91 (s, 2H), 2.47-2.25 (m, 8H), 2.15 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174978B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-885730bb68a144cb991ec2be0bb66ebd |
| Source note | uspto-grants-2015_11 |