HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340225Generated: October 27, 2026
Sodium Carbonate → HCID 58213667, compound
https://huagongshe.com/reaction/340225
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2-BOC-aminophenyl)boronic acid | HCID 2773226 | — |
| Reactant | 3-Chloro-5-vinylpicolinonitrile | HCID 66875225 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | HCID 58213667 | HCID 58213667 | — |
Reaction Steps
A solution of 2-(tert-butoxycarbonylamino)phenylboronic acid (1.0 eq.) and 3-chloro-5-vinylpicolinonitrile (from step 1) (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 vacuo 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 2-vinylbenzo[f][1,7]naphthyridin-5-amine as a yellow solid. 1H NMR (methanol-d4-CDCl3): δ 8.87 (d, 1H), 8.69 (d, 1H), 8.28 (d, 1H), 7.49-7.58 (m, 2H), 7.32 (dt, 1H), 6.90 (dd, 1H), 6.09 (d, 1H), 5.54 (d, 1H). LRMS [M+H]=222.1.
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-bd1b6a0b31084ce48f4432ad2109b781 |
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| Source note | uspto-grants-2014_11 |
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