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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492748Generated: October 30, 2026

Dimethylamine → HCID 23153431, compound

https://huagongshe.com/reaction/492748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant4-(4-Nitrophenoxy)pyridin-2-amineHCID 22936716—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23153431HCID 2315343172.5%

Reaction Steps

2-Amino-4-(4-nitrophenoxy)pyridine (761 mg) was dissolved in tetrahydrofuran (14 ml) under a nitrogen atmosphere, and then triethylamine (1.16 ml) and phenyl chloroformate (1.05 ml) were added dropwise while cooling in an ice water bath, followed by stirring for 30 min. To the reaction mixture was added 2 N dimethylamine (a solution in methanol) (6.95 ml), followed by stirring overnight. The reaction mixture was partitioned between ethyl acetate and a saturated aqueous solution of ammonium chloride. The organic layer was washed with a saturated aqueous solution of ammonium chloride, a saturated aqueous solution of sodium hydrogencarbonate, water and brine in this order, and dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure to give a residue, which was then purified by silica gel column chromatography (eluent; hexane:ethyl acetate=1:1 to 1:5). Fractions containing the target compound were concentrated under a reduced pressure to give a residue, which was then dried in vacuum to provide the titled compound (609 mg, 72.5%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-48213f1c90814e329cff33c6786d968d
Source noteuspto-grants-2009_05