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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236636Generated: October 26, 2026

Triethylamine → HCID 178467981, compound

https://huagongshe.com/reaction/2236636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(Aminomethyl)-2-(2-methoxyethoxy)phenolHCID 42625521—
Reactant(E)-6-bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dioneHCID 68692760—
SolventDimethylformamideHCID 6228—
ProductHCID 178467981HCID 17846798176.2%

Reaction Steps

An amount of (4E)-6-bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (0.40 g, 1.42 mmol) in 5 mL of N,N′-dimethylformamide is added 5-(aminomethyl)-2-(2-methoxyethoxy)phenol (0.33 g, 1.70 mmol) and 0.44 mL (4.26 mmol) of triethylamine. The reaction mixture is heated at room temperature overnight under N2. Mass spectroscopy suggested the completion of reaction. Reaction mixture is subsequently evaporated under high-pressure vacuum to brown solid. The solid is stirred in 5 mL of methanol for 10 min, then filtered, and washed in turn with 100 mL of water, 100 mL of methanol, and ether and hexane to afford 0.48 g (76.2% yield) of tan solid: mp 179-180° C.; MS (ESI) m/z 447.0-449.0 (M+H)+1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-dcff150d0f46479ba7c5adc48d3899ca
Source noteuspto-grants-2010_05