HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10302Generated: October 26, 2026
Triethylamine → 3-Chloro-2-cyclopropylamino-4,5-difluorobenzoic acid
https://huagongshe.com/reaction/10302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 2-Bromo-3-chloro-4,5-difluorobenzoic acid | HCID 21979471 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3-Chloro-2-cyclopropylamino-4,5-difluorobenzoic acid | HCID 21978933 | 63.7% |
Reaction Steps
In a sealed tube a mixture of 2-bromo-3-chloro-4,5-difluorobenzoic acid (Example 20, 7.96 g, 29.3 mmol), cyclopropyl amine (4.20 mL, 58.7 mmol), potassium acetate (5.77 g, 58.6 mmol), cupric acetate monohydrate (0.50 g, 2.5 mmol), and triethylamine (4.9 mL, 35.19 mmol) in isopropyl alcohol is stirred at 80° C. After 16 hours, the reaction mixture is concentrated under vacuum, and the resulting residue is dissolved in ethyl acetate. The organic layer is washed with 1.0 M hydrochloric acid, water, and brine. The organic layer is dried over MgSO4 and filtered. The filtrate is concentrated under vacuum and purified via flash column chromatography (5% isopropyl alcohol/1% formic acid/94% dichloromethane) to afford the title compound (4.62 g). MS CI: m/z 248 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094780B1 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ab04c13734c14f0eb76b4fd42879a70a |
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| Source note | uspto-grants-2006_08 |
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