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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808571Generated: October 27, 2026

Potassium Hydroxide → HCID 58054524, compound

https://huagongshe.com/reaction/1808571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-(Chloromethyl)benzamideHCID 458363—
Reactant4-Methoxy-1H-indazol-3-amineHCID 18526053—
ReactantHCID 86661402HCID 86661402—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 58054524HCID 5805452480%

Reaction Steps

To a solution of 4-(methyloxy)-1H-indazol-3-amine (for a preparation see Intermediate 1) (0.816 g, 5 mmol) in DMSO (50 mL) at room temperature under nitrogen was added potassium hydroxide (0.561 g, 10.0 mmol). After stirring the resulting deep red solution for 25 min 4-(chloromethyl)benzamide (0.848 g, 5.00 mmol) was added in one portion. The reaction mixture was stirred for a further 30 min and then poured into water (250 mL), forming an emulsion. The reaction mixture was extracted using chloroform (3×250 mL). The combined organic solutions were washed with water (250 mL) and passed through hydrophobic frit. The solvent was removed in vacuo and the residue was loaded in dichloromethane to a silica (100 g) cartridge and purified by chromatography on Flashmaster eluting with 0-100% ethyl acetate-cyclohexane+0-20% methanol-ethyl acetate over 60 min. The appropriate fractions were combined and evaporated in vacuo to give the title compound (1.18 g, 80%). LCMS: (System A) RT=0.69 min, ES+ve m/z 297 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357716B2
Source datasetuspto-grants-2013_01
ORD IDord-a16f704e027248808cd6d67c03378fe5
Source noteuspto-grants-2013_01