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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037535Generated: October 30, 2026

Methanol → 5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-N-methyl-6-[(methylsulfonyl)amino]-2H-indazole-3-carboxamide

https://huagongshe.com/reaction/1037535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 56962687HCID 56962687—
CatalystCopperHCID 23978—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventPyridineHCID 1049—
Product5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-N-methyl-6-[(methylsulfonyl)amino]-2H-indazole-3-carboxamideHCID 5696268817%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of Compound (1) (50 mg, 0.11 mmol), potassium carbonate (30 mg, 0.22 mmol), copper(I) iodide (10 mg, 0.05 mmol), copper (6.9 mg, 0.11 mmol) and 4-fluorophenol (18 mg, 0.16 mmol) in pyridine (1 mL) was heated to 150° C. for 16 h in a sealed-tube. After cooling to RT, MeOH (5 mL) was added and the mixture was filtered through celite and washed with more MeOH. The filtrate was concentrated in vacuo to give a crude mixture which was purified by reverse phase flash column chromatography eluting with ACN/water (10-100%) to give 5-cyclopropyl-2-[4-(4-fluorophenoxy)phenyl]-N-methyl-6-[(methylsulfonyl)amino]-2H-indazole-3-carboxamide (2) (9 mg, 17%) as a pale yellow solid. ESI-MS m/z calculated for [M+H]+: 495.15; found: 495.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546389B2
Source datasetuspto-grants-2013_10
ORD IDord-5c45a61abedc441494a8e144753fafb9
Source noteuspto-grants-2013_10