HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline → {6-[5-(4-Chlorophenyl)pyridin-2-ylethynyl]-4-methylquinolin-2-yl} methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline | HCID 86079850 | — |
| Reactant | 2-Bromo-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline | HCID 86079852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | {6-[5-(4-Chlorophenyl)pyridin-2-ylethynyl]-4-methylquinolin-2-yl} methylamine | HCID 69064008 | — |
Reaction Steps
Analogously to Example 1k, the following Examples may be prepared starting from 2-chloro-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline (Example 1h) or 2-bromo-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline (Example 1i) and the corresponding amines: Examples 1.8-1.9, 1.11, 1.15-1.21, 1.23 and 1.28 were prepared by heating in NMP in the microwave (300 W, 190° C.; 30-60 min); Example 1.13 was prepared by heating in DMF in the microwave (150 W, 170° C.; 10 min); and Example 1.51 was obtained as a by-product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524862B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-2e4afacdc5e44c009b05356c39df2ea5 |
| Source note | uspto-grants-2009_04 |