HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396674Generated: October 29, 2026
2-Pyridinesulfonamide, 3-iodo- → HCID 19044125, compound
https://huagongshe.com/reaction/2396674
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Pyridinesulfonamide, 3-iodo- | HCID 1214498 | — |
| Reactant | Methyl (4,6-dimethoxy-1,3,5-triazin-2-yl)carbamate | HCID 12803256 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19044125 | HCID 19044125 | — |
Reaction Steps
9.0 ml (18 mmol) of a 2M solution of trimethylaluminum in toluene are added dropwise at room temperature to 4.3 g (15 mmol) of 3-iodo-2-pyridinesulfonamide in 150 ml of dichloromethane. After evolution of gas has ceased, 3.85 [lacuna] (18 mmol) of methyl 4,6-dimethoxy-1,3,5-triazin-2-yl-carbamate in 20 ml of dichloromethane is added dropwise and the resulting solution is refluxed for 24 hours. The mixture is cooled and poured into 150 ml of ice-cold 1N hydrochloric acid. The organic phase is separated off and the aqueous phase is extractd 2× using dichloromethane. The organic phase is dried and evaporated. After triturating the crude product with diethyl ether, 3.1 g (44% of theory) of 3-(4,6-dimethoxy-1,3,5-triazin-2-yl)-1-(3-iodo-2-pyridylsulfonyl)urea of melting point 155 ° C. (dec.) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05494886 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-9513b68b87624a058b6ae942953ad969 |
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| Source note | uspto-grants-1996_02 |
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