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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl (4,6-dimethoxypyrimidin-2-yl)carbamateHCID 13314628—
ReactantBenzene-1,2-disulfonamideHCID 13885364—
ReactantTrimethylaluminumHCID 16682925—
CatalystHydrochloric AcidHCID 313—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductN-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1,2-benzenedisulfonamideHCID 1388536517%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04786316
Source datasetuspto-grants-1988_11
ORD IDord-1a7e31a84a8f4450b025d6221115b600
Source noteuspto-grants-1988_11