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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630486Generated: October 30, 2026

Ethanol → Methyl 1-(5-(3-methoxyphenyl)pyrimidin-2-yl)-3-(methylthio)-1H-indole-6-carboxylate

https://huagongshe.com/reaction/630486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant(3-Methoxyphenyl)boronic acidHCID 2734370—
ReactantMethyl 1-(5-bromopyrimidin-2-yl)-3-(methylthio)-1H-indole-6-carboxylateHCID 118666039—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 1-(5-(3-methoxyphenyl)pyrimidin-2-yl)-3-(methylthio)-1H-indole-6-carboxylateHCID 118676804—

Reaction Conditions

Temperature90 °C

Reaction Steps

Tetrakis(triphenylphosphine)palladium(0) (0.23 g, 0.20 mmol) and a 2M solution of sodium carbonate (8 mL) were added at room temperature and under an argon atmosphere to methyl 1-(5-bromopyrimidin-2-yl)-3-(methylthio)-1H-indole-6-carboxylate (3.0 g, 7.96 mmol) in DME (50 mL). The addition of 3-methoxy phenyl boronic acid (1.53 g, 9.94 mmol) and ethanol (50 mL) followed 10 min later, and the resulting mixture was heated at 90° C. for 5 h. The reaction mixture was then cooled to room temperature and filtered through a pad of celite. The filtrate was concentrated and the residue was purified by flash column chromatography [silica; ethyl acetate/hexane=3:7]. Yellow solid. Yield: 2.6 g (80% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315490B2
Source datasetuspto-grants-2016_04
ORD IDord-87a569e6bb1643e998ce3f2e03f891c4
Source noteuspto-grants-2016_04