Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991913Generated: October 29, 2026

N-Methoxy-N-methylacetamide → HCID 15224432, compound

https://huagongshe.com/reaction/991913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylacetamideHCID 537505—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 13958376HCID 13958376—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15224432HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465654B2
Source datasetuspto-grants-2002_10
ORD IDord-dcef6554cd104244b21d3e94507bb4bd
Source noteuspto-grants-2002_10