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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156611Generated: November 1, 2026

Hydrochloric Acid → HCID 20535101, compound

https://huagongshe.com/reaction/1156611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantHCID 20535125HCID 20535125—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 20535101HCID 20535101—

Reaction Conditions

Temperature0 °C

Reaction Steps

5.0 g. of 7-amino-5-diallylamino-2H-[1,2,4]oxadiazolo[2,3-a]-s-triazin-2-one are suspended in 7 ml. of triethylamine and 150 ml. of methylene chloride. 3.4 ml. of 4-chlorobenzoyl chloride in 35 ml. of methylene chloride are added dropwise while stirring and cooling to about 0° C. The mixture is subsequently stirred at about 0° C. for 1 hour. Water is then added thereto and the pH is adjusted to 4 with dilute hydrochloric acid solution. The two phases are separated and the aqueous phase is extracted twice with methylene chloride. The combined organic extracts are dried over sodium sulfate and evaporated to dryness under reduced pressure. The residue is recrystallized from methylene chloride and diethyl ether, there being obtained pure p-chloro-N-{5-diallylamino-2-oxo-2H-[1,2,4]oxadiazolo[2,3-a]-s-triazin-7-yl}benzamide having a melting point of 192°-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336380
Source datasetuspto-grants-1982_06
ORD IDord-645860eca69c44189d4d77f9644dc87f
Source noteuspto-grants-1982_06