Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907145Generated: November 1, 2026

Potassium Iodide → 6-amino-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid

https://huagongshe.com/reaction/1907145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantSodiumHCID 5360545—
Reactant6-amino-5-methyl-2H-indazole-7-carboxylic acidHCID 46855718—
SolventDimethylformamideHCID 6228—
Product6-amino-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acidHCID 58500429—

Reaction Steps

To a suspension of 6-amino-5-methyl-1H-indazole-7-carboxylic acid (0.956 g, 5 mmol) in dimethylformamide (4 ml) was added sodium hydrogenocarbonate (0.462 g, 5.5 mmol) and the resulting mixture was stirred at 40° C. for 15 minutes before 4-methoxybenzyl chloride (0.861 g, 5.5 mmol) was introduced. A catalytic amount of potassium iodide was added and the mixture was stirred for 18 hours at that temperature. After cooling down, the crude mixture was placed on top of a silica gel column and the product was purified by flash chromatography using a gradient starting from 50% ethyl acetate-50% cyclohexane to 100% ethyl acetate, then 1% acetic acid in ethyl acetate. The fractions containing the desired compound were evaporated and the residue was triturated with diethyl ether and filtered to yield light orange crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598078B2
Source datasetuspto-grants-2013_12
ORD IDord-9d1fc43bf4a54b69a3823e96147949bf
Source noteuspto-grants-2013_12