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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247002Generated: October 26, 2026

Hydrochloric Acid → 2-Chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]-N'-methylbenzenesulfonimidamide

https://huagongshe.com/reaction/247002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCarbamic acid, (4-methoxy-6-methyl-1,3,5-triazin-2-yl)-, phenyl esterHCID 11448329—
Reactant2-chloro-N'-methylbenzenesulfonimidamideHCID 20161053—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-aminocarbonyl]-N'-methylbenzenesulfonimidamideHCID 1392091022.5%

Reaction Steps

To a solution of 196.8 mg (0.96 mmol) of 2-chloro-N'-methylbenzenesulfonimidamide and 250 mg (0.96 mmol) of phenyl(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate in 5 mL of dry acetonitrile was added 0.15 mL (1.0 mmol) of 1,8-diazabicyclo[5.4.0]-undec-7-ene. After 45 minutes at room temperature, 5 mL of water and 2.5 mL of 5% HCl were added. The aqueous layer was extracted with methylene chloride (3×10 mL). The organic layer was dried (Na2SO4), filtered and the solvent was removed with a rotary evaporator. The residue was triturated with ethyl acetate to give 80 mg of a white solid; m.p. 154° to 160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705555
Source datasetuspto-grants-1987_11
ORD IDord-2bb6864443d34946aafac4f23f3ec10e
Source noteuspto-grants-1987_11