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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709316Generated: October 30, 2026

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

https://huagongshe.com/reaction/709316

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 numberUS09180127B2
Source datasetuspto-grants-2015_11
ORD IDord-619fa6f953524bc9bdc0115f70f31a2b
Source noteuspto-grants-2015_11