Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Picolyl chloride | HCID 23393 | — |
| Reactant | HCID 18422118 | HCID 18422118 | — |
| Product | HCID 18422078 | HCID 18422078 | 72% |
Reaction Steps
Using an analogous procedure to that described in Example 7 except that the reaction mixture was heated to 70° C. for 48 hours rather than to 40° C. for 18 hours, N-[3-(4-hydroxybenzamido)-4-methylphenyl]quinoline-6-carboxamide was reacted with 2-chloromethylpyridine to give the title compound in 72% yield; NMR Spectrum: (DMSOd6) 2.22 (s, 3H), 5.28 (s, 2H), 7.16 (d, 2H), 7.22 (d, 1H), 7.34 (m, 1H), 7.53 (m, 1H), 7.62 (m, 2H), 7.85 (m, 2H), 7.95 (m, 1H), 8.12 (d, 1H), 8.23 (m, 1H), 8.52 (m, 1H), 8.59 (m, 2H), 9.0 (d, 1H), 10.48 (s, 1H); Mass Spectrum: M+H+ 489.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06455520B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-8354e0e9de0a45688c050a34d19f65c4 |
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| Source note | uspto-grants-2002_09 |
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