HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Nitrobenzo[f][1,7]naphthyridin-5-amine → Benzo[f][1,7]naphthyridine-5,8-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Nitrobenzo[f][1,7]naphthyridin-5-amine | HCID 66891690 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Product | Benzo[f][1,7]naphthyridine-5,8-diamine | HCID 58213735 | — |
Reaction Steps
A mixture of 8-nitrobenzo[f][1,7]naphthyridin-5-amine (from the previous step) (1.0 eq) and Raney Nickel (wet, 10% wt) in EtOH/ammonia (2:1) was stirred under H2 balloon overnight. The reaction mixture was diluted with DCM. The insoluble solid was filtered off through celite, and the filtrate was concentrated en vacuo to obtain a crude residue. The crude material was washed with 10% MeOH/DCM and 70% EtOAc/Hexanes to give benzo[f][1,7]naphthyridine-5,8-diamine as an off white solid: 1H NMR (methanol-d4): δ 8.97 (dd, 1H), 8.90 (dd, 1H), 8.41 (d, 1H), 7.83 (dd, 1H), 7.57 (d, 1H), 7.39 (dd, 1H), 3.96 (s, 2). LRMS [M+H]=229.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895577B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-cd32b35f70fc4736998861954f9e4359 |
| Source note | uspto-grants-2014_11 |