Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382939Generated: October 30, 2026

Diisopropylethylamine → 1-(4-Fluoro-phenyl)-1H-indazole-4-carboxylic acid (6-bromo-pyridin-3-ylmethyl)-amide

https://huagongshe.com/reaction/2382939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-bromo-N-methylpyridin-3-amineHCID 817178—
Reactant1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid chlorideHCID 58138874—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(4-Fluoro-phenyl)-1H-indazole-4-carboxylic acid (6-bromo-pyridin-3-ylmethyl)-amideHCID 44469661—

Reaction Steps

A mixture of 1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid chloride (416 mg, 1.51 mmol), 6-bromo-pyridin-3-yl-methylamine (311 mg, 1.66 mmol) and DMAP (18.5 mg, 0.151 mmol) in DCM (10 mL) was treated with DIEA (1.32 mL, 7.56 mmol). The solution was stirred at room temperature. After 16 hours the mixture was diluted with DCM (30 mL). The organic layer was washed with saturated aqueous NH4Cl (2×10 mL), saturated aqueous NaHCO3 (2×10 mL), water (10 mL), brine (10 mL) and dried over MgSO4, filtered and concentrated. The residue was purified by silica gel chromatography eluting with a gradient of 0-50% ethyl acetate in hexanes to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263597B2
Source datasetuspto-grants-2012_09
ORD IDord-ac3a6a00c17c4c2997d1578d672ecefe
Source noteuspto-grants-2012_09