HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N'-Dimethylethylenediamine → HCID 68725213, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 43668381 | HCID 43668381 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 68725213 | HCID 68725213 | 38.2% |
Reaction Steps
4-Chloro-6-iodo-2-methylquinoline (0.61 g; see step (ii) above), 2-pyrrolidinone (0.24 g), copper (I) iodide (0.038 g), potassium phosphate (0.5 g) and N,N′-dimethylethylenediamine (0.035 g) in dimethylformamide (3 mL) were heated in a microwave at 100° C. for 1 hour. The reaction mixture was diluted with 1 N sodium hydroxide and extracted with ethyl acetate, washed with water, dried (MgSO4), filtered and evaporated. The residue was purified by chromatography on silica eluting with a mixture of dichloromethane, and methanol. The desired fractions were concentrated and the sample evaporated to dryness. Trituration from ether gave the title compound as a white powder (0.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759348B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-b5e93f6e838449da909eb75e95413def |
| Source note | uspto-grants-2014_06 |