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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293913Generated: October 28, 2026

Hydrochloric Acid → HCID 22027379, compound

https://huagongshe.com/reaction/2293913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamateHCID 14404501—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 21473067HCID 21473067—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 22027379HCID 2202737932.2%

Reaction Steps

14 mmol of trimethylaluminum (7 ml of a 2M solution in hexane) are added dropwise under a nitrogen protective atmosphere to a suspension of 3.6 g of 3-ethoxycarbonyl-2-iodobenzenesulfonamide in 100 ml of absolute dichloromethane. The mixture is stirred at room temperature for 30 minutes, and 2.2 g of O-methyl (4-methyl-6-methoxy-1,3,5-triazin-2-yl)carbamate in 25 ml of dichloromethane are then added, and the mixture is refluxed for 13 hours. The solution is cooled to room temperature, 25 ml of 2N hydrochloric acid are added dropwise with ice-cooling, and the hydrochloric acid phase is extracted twice using dichloromethane. The organic phase is concentrated in vacuo, and the residue is treated with acetone and 100 ml of 10% aqueous sodium acetate solution. The mixture is stirred for 3 hours and then filtered off with suction, followed by a washing step with diethyl ether, the aqueous phase is brought to pH 2-3 using concentrated hydrochloric acid and stirred for 15 minutes, and the product is filtered off with suction. After drying in vacuo at 50° C., 1.7 g of ethyl 2-iodo-3-[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]amino]sulfonyl]benzoate of m.p. 177°-9° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688745
Source datasetuspto-grants-1997_11
ORD IDord-9a68a1fce72440448a33c9316d8571cb
Source noteuspto-grants-1997_11