Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700545Generated: October 29, 2026

Hydrochloric Acid → HCID 178434177, compound

https://huagongshe.com/reaction/1700545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantHCID 178418668HCID 178418668—
Reactant3-Methyl-6-(2-chlorophenyl)-4,5,6,7-tetrahydroindazol-4-oneHCID 178434190—
SolventEthanolHCID 702—
ProductHCID 178434177HCID 17843417747%

Reaction Steps

A mixture of 6-(2-chlorophenyl)-3-methyl-4,5,6,7-tetrahydroindazol-4-one (1.05 g), aminoguanidine hydrochloride (0.47 g), concentrated hydrochloric acid (0.44 ml), water (0.44 ml) and ethanol (70 ml) was refluxed for 6 hours. Under reduced pressure, the solvent was evaporated, and to the residue was added sodium hydrogen carbonate solution. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated to give 4-guanidinoimino-6-(2-chlorophenyl)-3-methyl-4,5,6,7-tetrahydroindazole (0.6 g) as amorphous. To a solution of 4-guanidinoimino-6-(2-chlorophenyl)-3-methyl-4,5,6,7-tetrahydroindazole (0.3 g) in ethanol (10 ml) was added methanesulfonic acid (0.18 g), and the mixture was concentrated. The resulting crystals were recrystallized from water-ethanol to give 4-guanidinoimino-6-(2-chlorophenyl)-3-methyl-4,5,6,7-tetrahydroindazole methanesulfonate (Compound 22) (0.28 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-f795d2474f2848a69836d944ded62e81
Source noteuspto-grants-2002_02