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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503125Generated: October 30, 2026

Hydrochloric Acid → 1-Boc-3-bromo-5-nitro-1H-indazole

https://huagongshe.com/reaction/503125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
ReactantHCID 178526490HCID 178526490—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-3-bromo-5-nitro-1H-indazoleHCID 22260836—

Reaction Steps

To a solution of 24.0 g of 3-bromo-5-nitro-1H-indazole and 12.2 g of 4-(dimethylamino)pyridine in 50 ml tetrahydrofuran was added dropwise 23 ml of di-tert-butyl carbonate at room temperature. After stirring at room temperature for 30 minutes, the mixture was added with water, acidified by adding diluted hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:10), to give 20.5 g of the title compound as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776890B2
Source datasetuspto-grants-2010_08
ORD IDord-1bfcfca9c365478eb51478b11f314fd1
Source noteuspto-grants-2010_08