HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 86610971, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 66918943 | HCID 66918943 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86610971 | HCID 86610971 | — |
Reaction Steps
Using an analogous procedure to that described in Example 45, two equivalents of 1N methanesulfonic acid in ethyl acetate was reacted with N-cyclopropyl-3-[6-[3-(dimethylamino)propyl]-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.57 (m, 2H), 0.70 (m, 2H), 1.91 (s, 2H), 2.15 (s, 3H), 2.40 (s, 6H), 2.80 (d, 6H), 2.82-2.90 (m, 3H), 3.10 (m, 2H), 7.54 (d, 1H), 7.76 (d, 1H), 7.83 (m, 2H), 7.92 (m, 1H), 8.10 (d, 1H), 8.31 (s, 1H), 8.46 (d, 1H), 9.35 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750154B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-97a6754b4348456c816122bfb25122c7 |
| Source note | uspto-grants-2010_07 |