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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280814Generated: October 25, 2026

Hydrochloric Acid → Methyl 2-[[[4-(1-carboxyethoxy)-6-methyl-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoate

https://huagongshe.com/reaction/280814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSulphonyl diisocyanateHCID 77898—
ReactantBenzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
ReactantEthyl 2-[(4-amino-6-methyl-1,3,5-triazin-2-yl)oxy]propanoateHCID 19881799—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-[[[4-(1-carboxyethoxy)-6-methyl-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoateHCID 1364675023.8%

Reaction Steps

Methyl 2-(isocyanatosulfonyl)benzoate (10.1 g) and 8.0 g of ethyl 2-[(4-amino-6-methyl-1,3,5-triazin-2-yl)-oxy]propanoate were stirred in 80 ml of methylene chloride at ambient temperature for 18 hours. An additional 2 g of the sulfonylisocyanate was added and the reaction mixture was stirred for four more hours and then 2 g more of the sulfonylisocyanate was added. After stirring for four more hours at ambient temperature, 400 ml of water was added and the pH of this mixture was adjusted to pH 8 by the addition of 10% aqueous sodium hydroxide. The aqueous phase was separated and acidified to pH 1 with hydrochloric acid to precipitate a thick white gum. Sufficient 50% aqueous sodium hydroxide was added to achieve pH 12 and the mixture was heated on a steam bath until a clear solution resulted. The solution was again acidified with hydrochloric acid to pH 3 and the resultant cloudy solution was extracted with dichloromethane. The organic phase was dried and the solvent was removed to afford 3.7 g of the title compound as a glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591378
Source datasetuspto-grants-1986_05
ORD IDord-f16119571d7047ceb03c09aad7a2a8b5
Source noteuspto-grants-1986_05