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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947355Generated: October 31, 2026

Dimethylamine, hydrochloride → 8-acetyl-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

https://huagongshe.com/reaction/1947355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantDiisopropylethylamineHCID 81531—
Reactant8-acetyl-2-morpholino-4-oxo-4H-chromene-6-carboxylic acidHCID 58234981—
SolventDichloromethaneHCID 6344—
Product8-acetyl-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamideHCID 5823503446%

Reaction Steps

N-ethyl-N-isopropylpropan-2-amine (9.4 mL, 53.9 mmol) was added to 8-acetyl-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid (5.7 g, 18 mmol) in DCM (100 mL). Five minutes later dimethylamine hydrochloride (2.9 g, 35.9 mmol) and 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate (6.92 g, 21.6 mmol) were added. The mixture was diluted with DCM, washed with NaHCO3, dried over magnesium sulfate and concentrated to afford the crude product which was purified by flash chromatography on silica gel eluting with 0 to 5% MeOH/DCM. The solvent was evaporated to dryness to afford 8-acetyl-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide (2.75 g, 46%) as a yellow solid. Mass Spectrum: M+H+ 345.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399460B2
Source datasetuspto-grants-2013_03
ORD IDord-a3295f4939ef44a887728d7a01e5a6eb
Source noteuspto-grants-2013_03