HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 86610973, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 11751183 | HCID 11751183 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86610973 | HCID 86610973 | — |
Reaction Steps
Using an analogous procedure to that described in Example 45, a 0.1N solution of 4-toluenesulfonic acid in ethyl acetate was reacted N-cyclopropyl-3-[6-(4-isopropylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.57 (m, 2H), 0.71 (m, 2H), 1.32 (d, 6H), 2.14 (s, 3H), 2.29 (s, 3H), 2.86 (m, 1H), 3.11 (m, 2H), 3.22 (m, 2H), 3.53-3.63 (m, 3H), 4.09 (m, 2H), 7.11 (d, 2H), 7.49 (d, 2H), 7.54 (d, 1H), 7.58 (s, 1H), 7.72 (m, 2H), 7.83 (d, 1H), 7.91 (m, 1H), 8.17 (s, 1H), 8.45 (d, 1H), 9.31 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750154B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-6c6849c96a114b6aab331e2dd0214a15 |
| Source note | uspto-grants-2010_07 |