HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259115Generated: October 27, 2026
Sodium Carbonate → Ethyl 5-amino-8-methylbenzo[f][1,7]naphthyridine-2-carboxylate
https://huagongshe.com/reaction/1259115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Toluene ethanol | HCID 21863594 | — |
| Reactant | tert-Butyl (5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate | HCID 46737997 | — |
| Reactant | Ethyl 5-chloro-6-cyanonicotinate | HCID 66875248 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 5-amino-8-methylbenzo[f][1,7]naphthyridine-2-carboxylate | HCID 58213495 | — |
Reaction Steps
A solution of tert-butyl 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (from Example 5/step 2) (1.0 eq.) and ethyl 5-chloro-6-cyanonicotinate (from the previous step) (1.0 eq.), tetrakis(triphenyl-phosphine)palladium (5 mol %), and 2N aqueous sodium carbonate solution (2.0 eq.) in toluene/ethanol (2:1, 0.03 M) was stirred at 100° C. overnight. After cooling to ambient temperature, the reaction content was diluted with methanol. The insoluble solids were filtered off, and the filtrate was concentrated en vaccuo to obtain a crude residue. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give ethyl 5-amino-8-methylbenzo[f][1,7]naphthyridine-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466167B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-8f5d0e11b9944346a286f57c12f670f0 |
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| Source note | uspto-grants-2013_06 |
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