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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595675Generated: October 31, 2026

Dimethyl Sulfoxide → 2-Chloro-11-fluoro-5,6-dihydroindolo[2,1-a][2,6]naphthyridine

https://huagongshe.com/reaction/595675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(2-chloro-5-vinylpyridin-4-yl)-4-fluoro-1H-indoleHCID 90333567—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
Product2-Chloro-11-fluoro-5,6-dihydroindolo[2,1-a][2,6]naphthyridineHCID 9033346122.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 2-(2-chloro-5-vinylpyridin-4-yl)-4-fluoro-1H-indole (50 mg, 0.18 mmol), Bu4NCl (0.07 mL of 50% a.q. solution), DMSO (0.25 mL) and KOH (0.6 mL of 60% a.q. solution) was stirred at 100° C. for 3 hours. Then the mixture was diluted with H2O, extracted with EtOAc, then the combined organic phase was washed with brine, dried over Na2SO4 and concentrated in vacuo to give the crude product. It was purified by column (PE:EA=3:1) to obtain the product of 2-chloro-11-fluoro-5,6-dihydroindolo[2,1-a][2,6]naphthyridine (11 mg, yield: 20%). 1H-NMR (CDCl3, 400 MHz) δ 8.30 (s, 1H), 7.62 (s, 1H), 7.18˜7.21 (m, 2H), 7.12 (s, 1H), 6.81 (t, J=8.4 Hz, 1H), 4.29 (t, J=6.0 Hz, 2H), 3.20 (t, J=6.0 Hz, 2H). MS (M+H)+: 273/275.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243002B2
Source datasetuspto-grants-2016_01
ORD IDord-5469b66f999143ca927cc92efe775ebd
Source noteuspto-grants-2016_01