HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyltriphenylphosphonium bromide → 8-Phenethylbenzo[f][1,7]naphthyridin-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyltriphenylphosphonium bromide | HCID 2734970 | — |
| Reactant | 5-Aminobenzo[f][1,7]naphthyridine-8-carbaldehyde | HCID 86652355 | — |
| Product | 8-Phenethylbenzo[f][1,7]naphthyridin-5-amine | HCID 58213779 | — |
Reaction Steps
8-Phenethylbenzo[f][1,7]naphthyridin-5-amine was prepared from 5-aminobenzo[f][1,7]naphthyridine-8-carbaldehyde (from Example 87) with benzyltriphenylphosphonium bromide following the procedures described for Example 91 (wittig reaction) and Example 92 (reduction). 1H NMR (acetone-d6): δ 8.99 (dd, 1H), 8.88 (dd, 1H), 8.35 (d, 1H), 7.83 (dd, 1H), 7.49 (d, 1H), 7.29-7.15 (dd, 6H), 6.70 (br s, 2H), 3.10-3.00 (m, 4H). LRMS [M+H]=300.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09408907B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-760431f73c304af7b99020c7fe03e987 |
| Source note | uspto-grants-2016_08 |