HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methoxy-N-methylacetamide → HCID 15224432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 13958376 | HCID 13958376 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15224432 | HCID 15224432 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
2-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline (1 g, 4.2 mmol) was dissolved in anhydrous tetrahydrofuran (20 mL) then cooled to −78° C. A portion of lithium diisopropyl amide (2.8 mL, 4.2 mmol) was added dropwise to the cooled solution. At 10 minutes post addition, N-methoxy-N-methylacetamide (0.45 g, 4.4 mmol), prepared according to the method of T. A. Oster and T. M. Harris, Tetrahedron Letters, 24, 1851 (1983) was added. After 15 minutes the reaction was quenched with water and the resulting precipitate was collected and dried to provide the desired product as a solid. The structure was confirmed by nuclear magnetic resonance spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06348462B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-18d1e1f6e9ab475ca25a350d3a726ab8 |
| Source note | uspto-grants-2002_02 |