HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340313Generated: October 29, 2026
Potassium Carbonate → 8-Nitrobenzo[f][1,7]naphthyridin-5-amine
https://huagongshe.com/reaction/340313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromopyridine-2-carbonitrile | HCID 817694 | — |
| Reactant | Tert-butyl 5-nitro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate | HCID 66891429 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 8-Nitrobenzo[f][1,7]naphthyridin-5-amine | HCID 66891690 | — |
Reaction Steps
A solution of tert-butyl 5-nitro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (from the previous step) (1.0 eq.) and 3-bromopicolinonitrile (1.0 eq.) in toluene (0.44 M) was mixed with tetrakis(triphenyl-phosphine)palladium (5 mol %) and 2N aqueous potassium carbonate solution (2.0 eq.). The reaction was heated to 100° C. and stirred overnight. After cooling to ambient temperature, the reaction mixture was filtered to collect the precipitate. The precipitate was rinsed with EtOAc to give 8-nitrobenzo[f][1,7]naphthyridin-5-amine as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895577B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-da8e1dc0e3564cce94e8fdfd1786527f |
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| Source note | uspto-grants-2014_11 |
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