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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204480Generated: October 31, 2026

Ethyl Acetate → 1-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)ethanol

https://huagongshe.com/reaction/2204480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehydeHCID 58009883—
ReactantHCID 178418332HCID 178418332—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)ethanolHCID 5801020023%

Reaction Steps

To a solution of methylmagnesium chloride (0.232 mL, 0.697 mmol) in THF (10 mL) at about −78° C. was added a solution of 5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehyde (0.210 g, 0.697 mmol, Example #10, Step B) in DCM (10.0 mL). After about 10 min saturated aqueous NH4Cl was added to the reaction mixture. After warming to room temperature, EtOAc (30 mL) was added to the reaction mixture and the organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 20-80% EtOAc/heptane to provide 1-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)ethanol (0.050 g, 23%) as a yellow oil. LC/MS (Table 2, Method a) Rt=2.04 min; MS m/z: 318 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365579B2
Source datasetuspto-grants-2016_06
ORD IDord-c85c60a22d764796851d294ce2b69573
Source noteuspto-grants-2016_06