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 | US07008945B1 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-62f1751f1a6f44fd9aa8ae95f1f722f7 |
| Source note | uspto-grants-2006_03 |