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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902555Generated: October 26, 2026

1,2-Dimethoxyethane → 7-(2,4-dichloro-phenyl)-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazole

https://huagongshe.com/reaction/902555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(2,4-Dichlorophenyl)boronic acidHCID 2734659—
Reactant7-bromo-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazoleHCID 59702355—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product7-(2,4-dichloro-phenyl)-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazoleHCID 2109460288%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 7-bromo-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazole (1.47 g, 4.79 mmol), 2,4-dichlorophenyl boronic acid (1.32 g, 6.94 mmol), 18 mL of ethylene glycol dimethyl ether, tetrakis(triphenylphosphine)palladium(0) (0.166 g, 0.143 mmol), and 20 mL of a 2 M aqueous Na2CO3 solution was stirred at 85° C. overnight, then allowed to cool. Ethyl acetate (50 mL) was added, and the mixture was washed with two 40 mL portions of a saturated aqueous NaCl solution. The combined aqueous layers were extracted with 20 mL of ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, and concentrated to a brown oil. Column chromatography (0→5% EtOAc/hexanes) afforded 7-(2,4-dichloro-phenyl)-2-methyl-3-((E)-1-propyl-but-1-enyl)-2H-indazole (15a; 1.57 g; 88%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365211B2
Source datasetuspto-grants-2008_04
ORD IDord-603f9f3c47f2492ba555c6aee0832ff6
Source noteuspto-grants-2008_04