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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886310Generated: October 28, 2026

HCID 19875682, compound → HCID 19875683, compound

https://huagongshe.com/reaction/1886310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19875682HCID 19875682—
SolventHydrochloric AcidHCID 313—
ProductHCID 19875683HCID 19875683—

Reaction Steps

150 ml of 12N hydrochloric acid was added to 10 g of 4-(3-acetylaminophenyl)-3-methyl-5-mercaptotriazole (4) thus obtained. The system was then heated under reflux. After 3 hours, the system was cooled. Water was then distilled off by a rotary evaporator to obtain crystals of crude 4-(3-aminophenyl)-3-methyl-5-mercaptotriazole (5). 100 ml of acetonitrile was added to this crystal. 12 g of pyridine was then added to the system. The system was stirred. 7.5 g of phenyl chlorocarbonate was added dropwise to the system while the system was kept at a temperature of 5° C. or lower in an iced-water bath. After completion of the dropwise addition, the system was allowed to undergo reaction over 10 minutes. 20 ml of water was added to the reaction solution. The solvent was then distilled off by a rotary evaporator. The resulting concentrated solution was extracted with ethyl acetate. The extract was then washed with saturated aqueous solution of sodium chloride, and dried with sodium sulfate anhydride. The solvent was distilled off to obtain a crystals of crude 4-(3-phenoxycarbonylaminophenyl)-3-methyl-5-mercaptotriazole (6). The crude crystals were recrystallized from ethyl acetate to obtain 13 g of Compound (6). (Yield: 98%; m.p. 188° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151357
Source datasetuspto-grants-1992_09
ORD IDord-fd0da5ff47974d9fbb46798017057b77
Source noteuspto-grants-1992_09