HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224166Generated: October 27, 2026
Triethylamine → N-Cyclopropyl-N'-(2-fluoro-4-iodophenyl)urea
https://huagongshe.com/reaction/2224166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | N-Cyclopropyl-N'-(2-fluoro-4-iodophenyl)urea | HCID 59717054 | 95.5% |
Reaction Steps
Under a nitrogen atmosphere, to N,N-carbonyldiimidazole (82.1 g) were added N,N-dimethylformamide (400 ml) and triethylamine (70.5 ml), and a solution of 2-fluoro-4-iodoaniline 47 (100 g) in N,N-dimethylformamide (100 ml) was added dropwise under ice-cooling. After the completion of the dropwise addition, the mixture was stirred at room temperature for 5 hrs. The reaction mixture was ice-cooled, and cyclopropylamine (44.0 ml) was added dropwise. The mixture was stirred at room temperature for 1 hr, and the reaction mixture was added dropwise to water-toluene [2:1 (volume ratio), 1500 ml] with stirring. The precipitated crystals were collected by filtration and dried to give 1-cyclopropyl-3-(2-fluoro-4-iodo-phenyl)-urea 48 (129 g, yield 95.5%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07378423B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-e3c62755c0eb47b8b861e2fd50a5351e |
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| Source note | uspto-grants-2008_05 |
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