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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42661Generated: October 30, 2026

Methylamine → HCID 68701570, compound

https://huagongshe.com/reaction/42661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68702337HCID 68702337—
Reactant1-[3,4-Bis(benzyloxy)-5-nitrophenyl]-2-bromoethan-1-oneHCID 71445790—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 68701570HCID 68701570—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of methylamine (0.63 mL, 33% EtOH solution, 5 mmol) in a mixture of ethanol (25 mL) and acetic acid (0.5 mL) at room temperature was added ethyl 3-oxo-3-(2-(trifluoromethyl)pyridin-3-yl)propanoate (1.305 g, 5 mmol). The reaction mixture was heated at reflux for two hours whereupon the solvent was removed by evaporation under vacuum. To a solution of the crude product in dimethylformamide (25 mL) was added potassium carbonate (2.07 g, 15 mmol) in one portion followed by 1-(3,4-bis-benzyloxy-5-nitro-phenyl)-2-bromo-ethanone (2.51 g, 5.50 mmol) and the mixture was then stirred at 100° C. Once no starting material was detectable, the reaction mixture was allowed to cool to room temperature and poured onto ice-cold 1 N aqueous hydrochloric acid (100 mL). The resulting precipitate was filtered off, washed with water and dried. The residue was chromatographed over silica gel. Homogeneous fractions were pooled and evaporated to give ethyl 5-(3,4-bis(benzyloxy)-5-nitrophenyl)-1-methyl-2-(2-(trifluoromethyl)pyridin-3-yl)-1H-pyrrole-3-carboxylate, 2.492 g (79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536203B2
Source datasetuspto-grants-2013_09
ORD IDord-a3df68da885f4037b288775b0fd2c54d
Source noteuspto-grants-2013_09