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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199325Generated: November 1, 2026

2-Propanethiol → 4-(isopropylthio)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde

https://huagongshe.com/reaction/2199325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PropanethiolHCID 6364—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrrolo[2,3-b]pyridine-5-carbaldehydeHCID 86676739—
Solvent1,4-DioxaneHCID 31275—
Product4-(isopropylthio)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine-5-carbaldehydeHCID 8667674156.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-chloro-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (500 mg, 1.61 mmol) in dioxane (5 mL) were added K2CO3 (668 mg, 4.83 mmol) and 2-propanethiol (0.3 mL, 3.22 mmol). The reaction mixture was stirred for overnight for 70° C. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, celite filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using (5% to 20% Ethyl acetate/Hexane) as a solvent to afford title compound (320 mg, 56% yield). MS m/z: [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09358231B2
Source datasetuspto-grants-2016_06
ORD IDord-cd60ebc846a4491c8e38e9f9a14d6408
Source noteuspto-grants-2016_06