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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl indole-6-carboxylate | HCID 639844 | — |
| Reactant | Methyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylate | HCID 11175076 | — |
| Reactant | (4-Methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)boronic acid | HCID 67345879 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | methyl 3-cyclohexyl-2-(4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)-1H-indole-6-carboxylate | HCID 67345419 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989438B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-b0cc095db4904551b00e1131354d055c |
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| Source note | uspto-grants-2011_08 |
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