HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28048Generated: October 28, 2026
Benzenesulfonamide, N-(((4,6-dimethyl-2-pyrimidinyl)amino)carbonyl)-2-nitro- → HCID 13138213, compound
https://huagongshe.com/reaction/28048
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonamide, N-(((4,6-dimethyl-2-pyrimidinyl)amino)carbonyl)-2-nitro- | HCID 155933 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13138213 | HCID 13138213 | — |
Reaction Steps
A suspension containing 1 g of N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2-nitrobenzenesulfonamide, 0.2 g of 5% palladium on carbon and 50 ml of ethanol was shaken in a Paar apparatus under 40 p.s.i.g. hydrogen at ambient temperature. After one hour, the reaction mixture was filtered and the solids thereby recovered, which contained catalyst and desired product, was stirred with 10% aqueous sodium hydroxide. Filtration of that mixture and acidification of the filtrate with hydrochloric acid to pH 3 caused the desired product to precipitate. After removal by filtration and drying, the desired product melted at 212°-216° and showed infrared absorption peaks at 3200 and 3300 cm-1, consistent for the desired amino-containing compound. Mass spectrometry showed two particles of mass 198 and 123 units, equivalent to aminobenzenesulfonyl isocyanate and 2-amino-4,6-dimethylpyrimidine respectively, as expected for the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225337 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-00ce6b7df0914aeb9ed3f6c6da523116 |
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| Source note | uspto-grants-1980_09 |
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