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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669430Generated: October 29, 2026

Sodium Carbonate → methyl 3-cyclohexyl-2-(4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)-1H-indole-6-carboxylate

https://huagongshe.com/reaction/1669430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantMethyl indole-6-carboxylateHCID 639844—
ReactantMethyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylateHCID 11175076—
Reactant(4-Methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)boronic acidHCID 67345879—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Productmethyl 3-cyclohexyl-2-(4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)-1H-indole-6-carboxylateHCID 6734541981%

Reaction Conditions

Temperature110 °C

Reaction Steps

Methyl-2-bromo-3-cyclohexyl-1H-indole-6-carboxylate (prepared as described in International patent application WO2004/087714 from commercially available methyl indole-6-carboxylate) and (4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)boronic acid (1.1 eq) were dissolved in dioxane (0.125M solution) and 2M aq. Na2CO3 solution (3.3 eq) was added. The mixture was degassed and flushed with argon. Then Pd(PPh3)2Cl2 (0.1 eq) was added and the mixture was heated under argon atmosphere to 110° C. After 5 h at this temperature all volatiles were evaporated in vacuo and the residual material was dissolved in EtOAc. The solution was extracted with water and with brine, then dried over Na2SO4 and evaporated in vacuo. The residual material was purified by FC (PE:EtOAc, 9:1). After evaporation of the solvents the product was obtained as an off-white foam (81%). The material was used without further characterization in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989438B2
Source datasetuspto-grants-2011_08
ORD IDord-b0cc095db4904551b00e1131354d055c
Source noteuspto-grants-2011_08