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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916666Generated: November 2, 2026

Hydrogen Bromide → 5-Bromo-1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazole

https://huagongshe.com/reaction/1916666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1-(2-Pyrrolidin-1-YL-ethyl)-1H-indazol-5-ylamineHCID 11310777—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product5-Bromo-1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazoleHCID 57625541—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.00 g (4.34 mmol) 1-(2-pyrrolidin-1-yl-ethyl)-1H-indazol-5-ylamine is dissolved in 9.76 mL 48% hydrobromic acid and 9.76 mL water and the solution is cooled to 0° C. 2.5 M sodium nitrite solution (300 mg in 1.74 mL water) is slowly added dropwise. The reaction is stirred for 10 min at 0° C. and then a solution of 935 mg (6.51 mmol) CuBr in 3.42 mL 48% hydrobromic acid is added dropwise. The reaction is heated to 60° C. and stirred for one hour at this temperature. The mixture is diluted with water and the aqueous phase is extracted with EtOAc. The organic phase is discarded and the aqueous phase is made alkaline with saturated NaHCO3 solution. The aqueous phase is extracted with EtOAc and the organic phase is washed with water. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-ef632ad3988e451b9e13730e5e70c898
Source noteuspto-grants-2013_12