HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036903Generated: November 2, 2026
Aminoisobutyric acid → HCID 56966931, compound
https://huagongshe.com/reaction/1036903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 67290538 | HCID 67290538 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 56966931 | HCID 56966931 | — |
Reaction Steps
A solution of 2-(3-bromo-phenyl)-4,4,6-trimethyl-1,2,3,4-tetrahydro-quinoline (329.0 mg, 1.0 mmol), copper(I) iodide (57.0 mg, 0.3 mmol), 2-amino-2-methyl-propionic acid (309.0 mg, 3.0 mmol) and potassium carbonate (415.0 mg, 3.0 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 (150 mL×2), washed with water (50 mL×2) and saturated aqueous ammonium chloride solution (50 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) 2-methyl-2-[3-(4,4,6-trimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamino]-propionic acid (104.8 mg, 29%) as a white solid: LC/MS m/e obsd. (ESI+) [(M+H)+] 353.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546427B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-370c82461e7f45ae980019fe28f05aa5 |
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| Source note | uspto-grants-2013_10 |
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