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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515949Generated: October 30, 2026

1-(3-(3-methyl-1-(1H-pyrrolo[2,3-b]pyridin-2-yl)but-1-enyl)phenyl)ethanone → 1-{3-[3-methyl-1-(1H-pyrrolo[2,3-b]pyridin-2-yl)-butyl]-phenyl}-ethanone

https://huagongshe.com/reaction/1515949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-(3-methyl-1-(1H-pyrrolo[2,3-b]pyridin-2-yl)but-1-enyl)phenyl)ethanoneHCID 67229743—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1-{3-[3-methyl-1-(1H-pyrrolo[2,3-b]pyridin-2-yl)-butyl]-phenyl}-ethanoneHCID 5325014458.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1-(3-(3-methyl-1-(1H-pyrrolo[2,3-b]pyridin-2-yl)but-1-enyl)phenyl)ethanone (0.85 g, 2.8 mmol) in methanol (20 mL) and tetrahydrofuran (30 mL) was treated with 10% palladium on carbon (300 mg). The reaction was stirred for 16 h at 25° C. under hydrogen atmosphere. At this time, the reaction mixture was filtered. The filtrate was concentrated in vacuo. Silica gel column chromatography (20 g, 200-300 mesh, 10% ethyl acetate/petroleum ether) afforded 1-{3-[3-methyl-1-(1H-pyrrolo[2,3-b]pyridin-2-yl)-butyl]-phenyl}-ethanone (0.50 g, 58.3%) as an off-white solid: 1H NMR (300 MHz, d6-DMSO) δ ppm 11.63 (s, 1H), 8.09 (d, 1H, J=3.6 Hz), 7.96 (s, 1H), 7.81 (d, 2H, J=7.5 Hz), 7.66 (d, 1H, J=7.5 Hz), 7.46 (t, 1H, J=7.5 Hz), 6.98 (dd, 1H, J1=4.5 Hz, J2=8.1 Hz), 6.31 (s, 1H), 4.30 (t, 1H, J=8.1 Hz), 2.57 (s, 3H), 2.17-2.10 (m, 1H), 1.91-1.86 (m, 1H), 1.41-1.39 (m, 1H), 0.92 (s, 3H), 0.90 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222416B2
Source datasetuspto-grants-2012_07
ORD IDord-59b6af021531497ea4e07e3f1a5c44ad
Source noteuspto-grants-2012_07