HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586610Generated: November 4, 2026
Methanesulfonic Acid → HCID 15097348, compound
https://huagongshe.com/reaction/1586610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | HCID 19758586 | HCID 19758586 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15097348 | HCID 15097348 | 80.7% |
Reaction Steps
6.1 g of 2-furancarboxylic acid chloride and 0.1 g of 4-dimethylaminopyridine are added to a suspension of 10.1 g of 1-(3-sulfamoylphenyl)-3,3-dimethylurea in 60 ml of acetonitrile. 9.5 g of triethylamine are added dropwise to that mixture at room temperature. The reaction mixture is stirred for 15 hours at room temperature and for one hour at 60° C. After the mixture has cooled, 4.5 g of methanesulfonic acid are added dropwise thereto and the mixture is taken up in 1 liter of water. The oil that separates out crystallises after a short time. The crystals are separated off, washed with methanol and dried, yielding 11.3 g of 1-[3-(N-2-furylcarbonylsulfamoyl)-phenyl]-3,3-dimethylurea, m.p. 216°-217° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05215570 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-6f6b0d971a4742a886da5839a070fbc3 |
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| Source note | uspto-grants-1993_06 |
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