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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006621Generated: October 30, 2026

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

https://huagongshe.com/reaction/1006621

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 numberUS06790961B2
Source datasetuspto-grants-2004_09
ORD IDord-537f1149311d4d76a6c8446f768a7793
Source noteuspto-grants-2004_09