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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396976Generated: October 31, 2026

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

https://huagongshe.com/reaction/396976

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 numberUS06608201B2
Source datasetuspto-grants-2003_08
ORD IDord-72f3cb80bf0143bfbba9268d0d913d25
Source noteuspto-grants-2003_08