HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl bromide → HCID 44205296, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | 9-amino-5H-benzo[c][1,8]naphthyridin-6-one | HCID 58167951 | — |
| Product | HCID 44205296 | HCID 44205296 | 4.1% |
Reaction Steps
The title compound was synthesized according to the procedure described for the preparation of Example 458 using 70 (151 mg, 0.71 mmol) and 1-(bromo-methyl)-2-bromobenzene (214 mg, 0.86 mmol) to provide 469 (11 mg, 4% yield) as a white powder. LC-MS (M+H=381, obsd.=381). 1H NMR (400 MHz, DMSO-D6) δ 11.50 (m, 1H), 8.53 (m, 1H), 8.39 (m, 1H), 8.01 (d, J=8.9, 1H), 7.68 (s, 1H), 7.43 (m, 2H), 7.37 (s, 1H), 7.23 (s, 2H), 6.92 (m, 2H), 4.55 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735584B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-85b41a29774540b793709422496ce6f9 |
| Source note | uspto-grants-2014_05 |