HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloropyridine-4-carbonyl chloride → HCID 22238155, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloropyridine-4-carbonyl chloride | HCID 2800003 | — |
| Reactant | HCID 22238161 | HCID 22238161 | — |
| Product | HCID 22238155 | HCID 22238155 | — |
Reaction Steps
Using an analogous procedure to that described in Example 5, 3-(5-amino-2-methylphenyl)-6-(4-methylhomopiperazin-1-yl)-3,4-dihydroquinazolin-4-one was reacted with 2-chloropyridine-4-carbonyl chloride to give the title compound; NMR Spectrum: (DMSOd6) 1.84-1.96 (m, 2H), 2.06 (s, 3H), 2.29 (s, 3H), 2.42-2.49 (m, 2H), 2.62-2.68 (m, 2H), 3.53 (t, 2H), 3.58-3.64 (m, 2H), 7.22 (d, 1H), 7.34 (m, 1H), 7.44 (m, 1H), 7.58 (d, 1H), 7.73-7.78 (m, 2H), 7.82-7.86 (m, 1H), 7.96-7.98 (m, 2H), 8.50-8.62 (m, 1H), 10.68 (s, 1H); Mass Spectrum: M+H+503 & 505.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442704B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-a29ff9cbd8854ef7862414990ac8063b |
| Source note | uspto-grants-2008_10 |