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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338509Generated: November 1, 2026

Potassium Carbonate → Methyl 6-chloro-5-(4-(1-(hydroxymethyl)cyclobutyl)-3-methoxyphenyl)-1h-indole-3-carboxylate

https://huagongshe.com/reaction/338509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylateHCID 86698665—
Reactant[1-(4-Bromo-2-methoxyphenyl)cyclobutyl]methanolHCID 86698841—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 6-chloro-5-(4-(1-(hydroxymethyl)cyclobutyl)-3-methoxyphenyl)-1h-indole-3-carboxylateHCID 8669884283.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of [1-(4-bromo-2-methoxyphenyl)cyclobutyl]methanol (180 mg, 0.660 mmol) in dioxane (10 mL) and water (4 mL) was added methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate (213 mg, 0.660 mmol), Pd (dppf)Cl2 (48 mg, 0.070 mmol) and potassium carbonate (273 mg, 2.00 mmol). The reaction mixture was purged with nitrogen for 3 minutes and stirred at 80° C. for 2 hours. The mixture was extracted with dichloromethane. The organic phases were combined, dried over sodium sulfate, filtered, and concentrated in vacuo to give the title compound (220 mg, 83%) as a brown solid. It was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-bd70a4a666a64d8d8b3b754a95778537
Source noteuspto-grants-2014_11