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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614709Generated: November 1, 2026

Hydrochloric Acid → HCID 67792702, compound

https://huagongshe.com/reaction/1614709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 11054937HCID 11054937—
ReactantHCID 67792091HCID 67792091—
SolventDimethylacetamideHCID 31374—
ProductHCID 67792702HCID 67792702—

Reaction Steps

At room temperature, 166 mg (0.5 mmol) of methyl 2-(aminosulfonyl)-4-[(2,2,2-trifluoroethlidene)hydrazino]benzoate and 138 mg (0.5 mmol) of phenyl (4,6-dimethoxy1,3,5-triazin-2-yl)carbamate were dissolved in 1.5 ml of N,N-dimethylacetamide. Then, 86.1 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 6 hours. Thereafter, 0.2 ml of 35% hydrochloric acid was added to 30 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 as an eluent a 1:9 mixed solvent of methyl acetate and benzene, 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.). The title compound was obtained as a white solid. Yield: 103 mg (41%). Melting point: 117°-119° C. (foamed). Its physicochemical properties are shown in Table 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198566
Source datasetuspto-grants-1993_03
ORD IDord-aad90a35bdf94894b38f7b5b27eb973c
Source noteuspto-grants-1993_03