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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854398Generated: November 3, 2026

(E)-1-cyclohexyl-3-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)prop-2-en-1-one → 1-cyclohexyl-3-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)propan-1-one

https://huagongshe.com/reaction/1854398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-1-cyclohexyl-3-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)prop-2-en-1-oneHCID 58010004—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product1-cyclohexyl-3-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)propan-1-oneHCID 58010020101.3%

Reaction Steps

To a solution of (E)-1-cyclohexyl-3-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)prop-2-en-1-one (0.050 g, 0.12 mmol) in EtOAc (5 mL) was added palladium (10% on carbon, 0.0065 g, 0.0061 mmol). The reaction mixture was purged with hydrogen and a hydrogen atmosphere was maintained via balloon. After about 1 h at ambient temperature, the reaction mixture was filtered and concentrated under reduced pressure to provide 1-cyclohexyl-3-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)propan-1-one as an oil (0.050 g, 100%): LC/MS (Table 2, Method a) Rt=2.94 min; MS m/z: 412 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962629B2
Source datasetuspto-grants-2015_02
ORD IDord-6061b0d792b14c1883dbf8f6af2074f0
Source noteuspto-grants-2015_02