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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653992Generated: October 30, 2026

Hydrochloric Acid → HCID 14857997, compound

https://huagongshe.com/reaction/653992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCarbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl esterHCID 10945667—
ReactantHCID 14857993HCID 14857993—
SolventDimethylacetamideHCID 31374—
ProductHCID 14857997HCID 14857997—

Reaction Steps

At room temperature, 158 mg (0.43 mmol) of ethyl -2-(aminosulfonyl)-4-[(2,5-dihydro-3,4-dimethyl-2,5-dioxo-1H-pyrrol-1-yl)amino]benzoate and 118 mg (0.43 mmol) of phenyl (4,6-dimethoxypyrimidin-2-yl)carbamate were dissolved in 1.5 ml of N,N-dimethylacetamide. Then, 73 mg of 1,8-diazabicyclo[5.4.0]undec-7-ene were added, followed by stirring for 5 minutes. The resultant mixture was allowed to stand for 15 hours. Thereafter, 0.2 ml of 35% hydrochloric acid was added to 20 ml of ice water, followed by the addition of the reaction mixture in 0.2 ml portions under stirring. After the reaction mixture was stirred for 20 minutes, the resulting precipitate was collected by filtration and dried in air. Using dichloromethane as an eluent, the crude product was purified by chromatography on a column of silica gel ("WAKO GEL C-300", trade name; product of Wako Pure Chemical Industries, Ltd.). Yield: 162 mg (58%). Melting point: 121°-123 ° C. (decomposed). Its physicochemical properties are shown in Table 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05129942
Source datasetuspto-grants-1992_07
ORD IDord-aacfbf21c30f48d19d09d9d65fee8c6a
Source noteuspto-grants-1992_07