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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678716Generated: October 27, 2026

Hydrochloric Acid → HCID 178434358, compound

https://huagongshe.com/reaction/1678716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1-Benzyl-3-methyl-1H-indazol-6-olHCID 135780250—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 178434358HCID 178434358—

Reaction Conditions

Temperature60 °C

Reaction Steps

1-Benzyl-3-methylindazol-6-ol (16.7410 g) and 10% palladium-carbon-PE-type-50% wet with water (5.1164 g; manufactured by N.E. Chemcat Corp.) were suspended in ethanol (166 mL), and then concentrated hydrochloric acid (5.83 mL; manufactured by Kanto Chemical Co., Inc.) was added thereto. The reaction system was purged with hydrogen, and under a hydrogen atmosphere, the reaction solution was stirred for 10 hours at 60° C. The reaction solution was cooled to room temperature, and then the reaction system was purged with nitrogen. 10% Palladium on carbon-PE-type-50% wet with water (1.5059 g; manufactured by N.E. Chemcat Corp.) was added to the reaction solution, and the reaction system was purged with hydrogen. Under a hydrogen atmosphere, the reaction solution was stirred for 5 hours at 60° C. The reaction solution was cooled to room temperature, and the reaction system was purged with nitrogen. Subsequently, the reaction solution was filtered, and the solvent was evaporated under reduced pressure from the filtrate. Ethyl acetate was added to the resulting residue, and the mixture was washed once with a saturated aqueous solution of sodium hydrogen carbonate. The organic layer was washed once with a saturated sodium hydrogen carbonate solution, and then was dried over sodium sulfate. The solvent was evaporated under reduced pressure from the organic layer, and thus the title compound was obtained as a crude product (10.816 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008506B2
Source datasetuspto-grants-2011_08
ORD IDord-eeb5041995c147fe87b1708cdde9dea3
Source noteuspto-grants-2011_08