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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204542Generated: November 1, 2026

Ethyl Acetate → 5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehyde

https://huagongshe.com/reaction/2204542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium periodateHCID 23667635—
ReactantHCID 58009875HCID 58009875—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehydeHCID 5800988380%

Reaction Steps

To a solution of (E)-2-styryl-5-tosyl-5H-pyrrolo[2,3-b]pyrazine (1.2 g, 3.2 mmol) in 1,4-dioxane (20 mL) and water (2.0 mL) was added sodium periodate (2.73 g, 12.8 mmol) followed by osmium tetroxide (2.5% in t-BuOH, 4.01 mL, 0.320 mmol). After about 1 day at ambient temperature, additional sodium periodate (2.73 g, 12.78 mmol) and osmium tetroxide (2.5% in t-BuOH, 4.01 mL, 0.320 mmol) were added. After about 2 days, a solution of aqueous Na2S2O3 (100 mL) and EtOAc (100 mL) was added. The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting solid was triturated with heptane to remove benzaldehyde. The resulting solid was dried in vacuo to provide 5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehyde as a brown solid (0.77 g, 80%): LC/MS (Table 2, Method a) Rt=2.01 min; MS m/z: 334 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365579B2
Source datasetuspto-grants-2016_06
ORD IDord-9d35a372e2544ddf876d85617a213a20
Source noteuspto-grants-2016_06