HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75665Generated: October 29, 2026
Methylamine → 1-(2-Fluoro-4-iodophenyl)-3-methylurea
https://huagongshe.com/reaction/75665
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | 1-(2-Fluoro-4-iodophenyl)-3-methylurea | HCID 59717351 | 94.8% |
Reaction Steps
Under a nitrogen atmosphere, to N,N-carbonyldiimidazole (61.4 g) were added N,N-dimethylformamide (300 ml) and triethylamine (52.8 ml) and a solution of 2-fluoro-4-iodoaniline 47 (74.8 g) in N,N-dimethylformamide (75 ml) was added dropwise with stirring 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 a solution (60 ml) of 40% methylamine in methanol 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), 1125 ml] under stirring. The precipitated crystals were collected by filtration and dried to give 1-(2-fluoro-4-iodophenyl)-3-methylurea 63 (87.9 g, yield 94.8%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835443B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-9f5faabee287429ebdb6145a23e54304 |
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| Source note | uspto-grants-2014_09 |
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