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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(2-chloro-5-vinylpyridin-4-yl)-4-fluoro-1H-indole | HCID 90333567 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-11-fluoro-5,6-dihydroindolo[2,1-a][2,6]naphthyridine | HCID 90333461 | 22.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09243002B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-5469b66f999143ca927cc92efe775ebd |
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| Source note | uspto-grants-2016_01 |
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