HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408147Generated: October 30, 2026
1-Aminocyclopropane-1-carboxylic acid → HCID 59053938, compound
https://huagongshe.com/reaction/2408147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Aminocyclopropane-1-carboxylic acid | HCID 535 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 70496424 | HCID 70496424 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 59053938 | HCID 59053938 | 47% |
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), 1-amino-cyclopropanecarboxylic 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 1-[3-(6-cyclobutylsulfamoyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-5-fluoro-phenylamino]-cyclopropanecarboxylic acid (73.2 mg, 47.0%) as a white solid: MS (ESI) M+1=488.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809369B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-e5c0f433be4e4b49a670e0031208c421 |
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| Source note | uspto-grants-2014_08 |
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