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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408146Generated: October 31, 2026

Aminoisobutyric acid → HCID 59053883, compound

https://huagongshe.com/reaction/2408146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoisobutyric acidHCID 6119—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 70496424HCID 70496424—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 59053883HCID 5905388351%

Reaction Steps

A mixture solution of 2-(3-bromo-5-fluoro-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-sulfonic acid cyclobutylamide (150 mg, 0.32 mmol), copper(I) iodide (20 mg, 0.1 mmol), 2-amino-2-methyl-propionic acid (135 mg, 1.3 mmol) and potassium carbonate (140 mg, 1.0 mmol) in dimethyl sulfoxide (2.0 mL) was stirred at 120° C. for 16 h. Then the reaction mixture was cooled to room temperature and extracted with ethyl acetate (70 mL×2), washed with water (30 mL×3) and saturated aqueous ammonium chloride solution (30 mL×2), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by Waters automated flash system (column: Xterra 30 mm×100 mm, sample manager 2767, pump 2525, detector: ZQ mass and UV 2487, solvent system: acetonitrile and 0.1% ammonium hydroxide in water) afforded 2-[3-(6-cyclobutylsulfamoyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-5-fluoro-phenylamino]-2-methyl-propionic acid (79.8 mg, 51.0%) as a white solid: MS (ESI) M+1=490.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-1d466d39af0942788ddcb8f4250bf2a5
Source noteuspto-grants-2014_08