Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156618Generated: November 1, 2026

Hydrochloric Acid → HCID 20535105, compound

https://huagongshe.com/reaction/1156618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantHCID 20535125HCID 20535125—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 20535105HCID 20535105—

Reaction Conditions

Temperature5 °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 100 ml. of methylene chloride and 10 ml. of triethylamine. 2.5 g. of methoxyacetyl chloride in 20 ml. of methylene chloride are added dropwise while stirring and cooling to about 5° C. After 1 hour at about 5° C., the mixture is treated with water and adjusted to pH 4 with 3-N hydrochloric acid. The two phases are separated and the aqueous phase is extracted with methylene chloride. The combined organic extracts are dried over sodium sulfate and evaporated under reduced pressure. The residue is recrystallized from methylene chloride and diethyl ether, there being obtained N-{5-diallylamino-2-oxo-2H-[1,2,4]oxadiazolo[2,3-a]-s-triazin-7-yl}-2-methoxyacetamide having a melting point of 135°-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336380
Source datasetuspto-grants-1982_06
ORD IDord-cb2a44b0bc994c5dba21b152a242ebfc
Source noteuspto-grants-1982_06