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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387473Generated: November 1, 2026

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

https://huagongshe.com/reaction/2387473

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 5762554125%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of NaNO2 (0.20 g, 2.8 mmol) in H2O (5 mL) was cooled in a wet ice bath and treated with a solution of 1-(2-(pyrrolidin-1-yl)ethyl)-1H-indazol-5-amine (0.65 g, 2.8 mmol) in 48% aqueous HBr (2 mL). The resulting mixture was added to a pre-heated solution of CuBr (0.49 g, 3.4 mmol) in 48% aqueous HBr (2 mL) at 100° C. After stirring at 100° C. for 15 min, the dark mixture was allowed to cool. The solids were isolated by filtration, washed with 1N NaOH, and dried under vacuum. Purification by flash column chromatography (silica gel, CH2Cl2/MeOH, 95:5 to 90:10) gave the title compound (0.21 g, 25%) as a brown solid ESI MS m/z 294 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268868B2
Source datasetuspto-grants-2012_09
ORD IDord-09bf734f49204882a6a4529634bf291f
Source noteuspto-grants-2012_09