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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530314Generated: November 1, 2026

Sulfamide → HCID 66681709, compound

https://huagongshe.com/reaction/530314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamideHCID 82267—
ReactantHCID 66682011HCID 66682011—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66681709HCID 666817096%

Reaction Steps

Sulfamide (0.089 g, 0.922 mmol) was added to a stirred suspension of 4-(4-aminophenyl)-N-cyclohexyl-N-methyl-1H-imidazole-1-carboxamide (0.250 g, 0.838 mmol) in dioxane (2 mL) at room temperature. The suspension was heated at reflux for 4 h to give a clear solution, whereupon more sulfamide (0.089 g, 0.922 mmol) was added and the mixture was heated at reflux for a further 2.5 h. The solvent was removed and the brown residue was purified by chromatography (silica, dichloromethane/methanol, 1%, 2%, 5%). Homogenous fractions were pooled and evaporated. The residue was triturated with ethyl acetate and the colourless solid that formed was removed by filtration. The filtrate was evaporated and purified again by preparative TLC (silica, dichloromethane/10% methanol). The product was extracted from the silica with a mixture of ethyl acetate/10% methanol. Evaporation of the solvent gave a clear oil, that was triturated with a mixture of ethyl acetate and methanol to give the product as an off-white solid (19 mg, 6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353082B2
Source datasetuspto-grants-2016_05
ORD IDord-3395a83747bf4d49b7958248e8f0a525
Source noteuspto-grants-2016_05