HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232017Generated: October 28, 2026
Water → N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1,2-benzenedisulfonamide
https://huagongshe.com/reaction/2232017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl (4,6-dimethoxypyrimidin-2-yl)carbamate | HCID 13314628 | — |
| Reactant | Benzene-1,2-disulfonamide | HCID 13885364 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1,2-benzenedisulfonamide | HCID 13885365 | 17% |
Reaction Steps
To a suspension of 0.7 g of 1,2-benzenedisulfonamide and 1.5 ml of trimethylaluminum in 70 ml of anhydrous methylene chloride was added 0.6 g of 4,6-dimethoxypyrimidin-2-ylcarbamic acid methyl ester under N2 with stirring. After addition, the mixture was stirred at room temperature for 30 minutes and was then heated to reflux for 12 hours. The reaction mixture was then cooled down to room temperature. To this mixture was added 50 ml of methylene chloride, 100 ml of water, 10 ml of acetic acid and 5 drops of concentrated hydrochloric acid. The mixture was then stirred at room temperature for 20 minutes and was filtered. The organic layer was then separated, washed with water, dried over sodium sulfate and concentrated. The residue was then chromatographed on silica gel (CH2Cl2 /acetic acid 1:1) to yield 0.2 g of N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1,2-benzenedisulfonamide, m.p. 192°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04786316 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-1a7e31a84a8f4450b025d6221115b600 |
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| Source note | uspto-grants-1988_11 |
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