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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699694Generated: October 30, 2026

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

https://huagongshe.com/reaction/1699694

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 numberUS06348462B1
Source datasetuspto-grants-2002_02
ORD IDord-18d1e1f6e9ab475ca25a350d3a726ab8
Source noteuspto-grants-2002_02