HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023704Generated: November 3, 2026
Cyanuric chloride → Methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate
https://huagongshe.com/reaction/1023704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-aminobenzoate | HCID 12082 | — |
| Reactant | 4,5-Diisopropylfuran-2-carboxylic acid | HCID 58420514 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate | HCID 67395533 | 89.3% |
Reaction Steps
A solution of 4,5-diisopropylfuran-2-carboxylic acid (50 mg, 0.255 mmol) and cyanuric chloride (71 mg, 0.385 mmol) in acetone (3 ml) was added with triethylamine (142 μl, 1.021 mmol), and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with methyl 4-aminobenzoate (77 mg, 0.510 mmol), and the mixture was further stirred for 14 hours. The reaction solvent was evaporated, then the residue was dissolved in pyridine (1 ml), the solution was added with 4-dimethylaminopyridine (1 mg, 8.20 μmol), and the mixture was stirred at room temperature for 4 hours. Pyridine was evaporated, and then the reaction mixture was dissolved in 10% methanol-chloroform, the solution was added with silica gel (1.0 g), and the mixture was evaporated to dryness. The residue was purified by silica gel chromatography [hexane-ethyl acetate (6:1)] to obtain methyl 4-[(4,5-diisopropylfuran-2-carbonyl)amino]benzoate (75 mg, 89%) as colorless prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722730B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-a939961a1e2345c4ad57a37bd8d47e01 |
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| Source note | uspto-grants-2014_05 |
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