HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetate → 6-acetylamino-1-(3-methylbenzyl)-4-methylhexahydro-1H-1,4-diazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetate | HCID 175 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | m-Xylyl chloride | HCID 12102 | — |
| Reactant | 6-acetylamino-1-methylhexahydro-1H-1,4-diazepine | HCID 15206155 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 6-acetylamino-1-(3-methylbenzyl)-4-methylhexahydro-1H-1,4-diazepine | HCID 14998991 | — |
Reaction Steps
A mixture of acetate of 6-acetylamino-1-methylhexahydro-1H-1,4-diazepine (3.0 g), 3-methylbenzyl chloride (3.5 g), potassium carbonate (17 g), sodium iodide (0.1 g) and methyl ethyl ketone (200 ml) is refluxed with stirring for 16 hours. The reaction mixture is filtered, and the filtrate is concentrated under reduced pressure. The residue is chromatographed on silica gel with elution of chloroform-methanol (20:1). Fractions containing the title compound are pooled and evaporated under reduced pressure to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166341 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-ad9e5766f2a34d56ae5126485c82708d |
| Source note | uspto-grants-1992_11 |