HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzyl bromide → [5-(4-Fluoro-benzyloxy)-quinolin-2-yl]-(5-methyl-furan-2-ylmethyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | 5-Methyl-2-furylmethylamine | HCID 2724683 | — |
| Reactant | 2-chloroquinolin-5-ol | HCID 135442221 | — |
| Product | [5-(4-Fluoro-benzyloxy)-quinolin-2-yl]-(5-methyl-furan-2-ylmethyl)-amine | HCID 68436831 | — |
Reaction Steps
The title compound, MS: m/e=363.3 (M+H+), was prepared in accordance with the general method of example 63 from 5-hydroxy-2-chloroquinoline (CAS 124467-35-2), 5-methyl-2-furanmethanamine and 4-fluoro-benzyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825253B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-51b285be26aa43a6af0ca4b53b0ce228 |
| Source note | uspto-grants-2010_11 |