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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507439Generated: October 29, 2026

Diisopropylethylamine → HCID 71668098, compound

https://huagongshe.com/reaction/1507439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3,3,3-Trifluoropropionic acidHCID 2777972—
ReactantHCID 117701633HCID 117701633—
SolventDimethylformamideHCID 6228—
ProductHCID 71668098HCID 7166809813.6%

Reaction Steps

A solution of 7-hydroxy-3,8-dimethyl-2-(piperidin-4-yl)-4H-chromen-4-one (68 mg, 0.25 mmol) obtained in Example 7-2, 3,3,3-trifluoropropionic acid (33 μL, 0.30 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (192 mg, 1.00 mmol), and diisopropylethylamine (86 μL, 0.50 mmol) in dimethylformamide (1.5 mL) was stirred at room temperature for 4 hours. The reaction solution was concentrated, and water was added to the obtained residue, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate. The desiccant was filtered off, and then the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol=100/0→95/5) to obtain 13 mg of the title compound (yield: 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221811B2
Source datasetuspto-grants-2015_12
ORD IDord-18e863f3e50940b9a9caaff2a01e4fe0
Source noteuspto-grants-2015_12