HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 2-Chloro-N-methyl-4-(4-methyl-piperazin-1-yl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-chloro-4-fluoro-N-methylbenzamide | HCID 17144535 | — |
| Product | 2-Chloro-N-methyl-4-(4-methyl-piperazin-1-yl)-benzamide | HCID 18546503 | 52.5% |
Reaction Steps
A mixture of 316 mg (1.68 mmol) 2-chloro-4-fluoro-N-methyl-benzamide and 0.94 ml (8.4 mmol) 1-methylpiperazine was heated at 140° for 7 h in a sealed glass tube. After cooling to room temperature excess 1-methylpiperazine was removed by distillation at 50°/0.5 mbar. The residue was partitioned between 25 ml CH2Cl2/2 N NaOH solution. The layers were separated and the aqueous layer was extracted with 3 15-ml portions of dichloromethane. The combined organic extracts were dried (Na2SO4) and evaporated. Chromatography (SiO2, CH2Cl2/methanol 19:1) yielded 236 mg (52%) 2-Chloro-N-methyl-4-(4-methyl-piperazin-1-yl)-benzamide as a light yellow solid, MS (EI): 267 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06552088B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-8e176263995a49bfb7a69150c243181a |
| Source note | uspto-grants-2003_04 |