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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274760Generated: November 1, 2026

Dichloromethane → 6-fluoro-3-(1-methyl-1H-pyrazol-4-yl)-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/2274760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium AcetateHCID 517044—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant3-Bromo-6-fluoro-1-(phenylsulfonyl)-1H-indoleHCID 86346249—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
Product6-fluoro-3-(1-methyl-1H-pyrazol-4-yl)-1-(phenylsulfonyl)-1H-indoleHCID 11806053723%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-bromo-6-fluoro-1-(phenylsulfonyl)-1H-indole (Intermediate 2; 1.0 g; 2.8 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.7 g; 8.4 mmol), KOAc (1.4 g; 14.0 mmol) and Pd(dppf)Cl2.CH2Cl2 (0.15 g; 0.18 mmol) in DMF (25 mL) flushed with nitrogen was heated to 90° C. overnight. The mixture was filtered through Celite, diluted with EtOAc (10 mL) and water (10 mL). The aqueous layer was extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered, concentrated, and purified by a silica gel chromatography (petroleum ether/EtOAc=1/1) to afford 0.20 g (23%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126984B2
Source datasetuspto-grants-2015_09
ORD IDord-73c495d7db6f4de697b33bda1c0e82e8
Source noteuspto-grants-2015_09