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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943866Generated: November 3, 2026

HCID 67088905, compound → HCID 67089079, compound

https://huagongshe.com/reaction/1943866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67088905HCID 67088905—
SolventEthyl AcetateHCID 8857—
ProductHCID 67089079HCID 6708907992%

Reaction Steps

SnCl2 dihydrate (0.85 g, 3.79 mmol) was added to a suspension of 3-bromo-5-nitro-1-tosyl-1H-indazole (0.300 g, 0.76 mmol) in ethyl acetate (25 mL), and the reaction mixture was heated to reflux overnight. The reaction mixture was cooled to room temperature and quenched with saturated NaHCO3 (25 mL). The resulting suspension was filtered through a pad of celite, and the filter cake was washed with ethyl acetate (100 mL). The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried, filtered and concentrated. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (1:1) to give 3-bromo-1-tosyl-1H-indazol-5-amine (0.256 g, 92%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-5331db065aa045cea5ce3b2b3832e0d3
Source noteuspto-grants-2013_03