HuagongsheHuagongshe Chemistry Print Report · For research reference only
Picolyl chloride → HCID 18422110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Picolyl chloride | HCID 23393 | — |
| Reactant | HCID 18422129 | HCID 18422129 | — |
| Product | HCID 18422110 | HCID 18422110 | 58% |
Reaction Steps
Using an analogous procedure to that described in Example 7, N-[3-(3-hydroxybenzamido)-4-methylphenyl]quinoline-6-carboxamide was reacted with 2-chloromethylpyridine to give the title compound in 58% yield; NMR Spectrum: (DMSOd6) 2.2 (s, 3H), 5.26 (s, 2H), 7.23 (m, 2H), 7.33 (t, 1H), 7.43 (t, 1H), 7.57 (t, 1H), 7.61 (m, 4H), 7.82 (m, 1H), 7.85 (d, 1H), 8.12 (d, 1H), 8.25 (d, 1H), 8.51 (d, 1H), 8.58 (d, 1H), 8.61 (s, 1H), 8.99 (d, 1H), 9.9 (s, 1H), 10.48 (s, 1H); Mass Spectrum: M+H+ 489.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455520B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-66433e19b83648adbcf5882d79ee2ff4 |
| Source note | uspto-grants-2002_09 |