HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 6-chloro-N-methyl-4-o-tolyl-nicotinamide | HCID 12167312 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide | HCID 15481065 | 83.7% |
Reaction Steps
A solution of 3.2 g (12.2 mmol) 6-chloro-N-methyl-4-o-tolyl-nicotinamide in 6.7 ml (60.3 mmol) 1-methylpiperazine was stirred at 100° C. for 2.5 h. The reaction mixture was cooled to r.t., treated with 10 ml 0.1N NaOH and extracted. The aqueous phase was separated and extracted twice with THF and the organic phases were washed twice with brine. The combined organic phases were dried over Na2SO4, the solvent was removed under reduced pressure and the residue purified by chromatography over silica gel (CH2Cl2: MeOH=99:1) to yield 3.3 g (83.7%) product as beige foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297375B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-eefe8b99b07941b6a93ec93469bdf05b |
| Source note | uspto-grants-2001_10 |