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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854330Generated: November 1, 2026

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

https://huagongshe.com/reaction/1854330

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 numberUS08962629B2
Source datasetuspto-grants-2015_02
ORD IDord-8db169e3724849e8884f65d5f865cc9c
Source noteuspto-grants-2015_02