HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 86610966, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 66919015 | HCID 66919015 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86610966 | HCID 86610966 | — |
Reaction Steps
Using an analogous procedure to that described in Example 45, 1N methanesulfonic acid in ethyl acetate was reacted with N-cyclopropyl-3-[6-{[2-(dimethylamino)ethyl]thio}-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.70 (m, 2H), 2.15 (s, 3H), 2.33 (s, 3H), 2.85 (m, 7H), 3.32 (m, 2H), 3.45 (m, 2H), 7.53 (d, 1H), 7.79 (d, 1H), 7.83 (s, 1H), 7.90-7.97 (m, 2H), 8.17 (s, 1H), 8.32 (s, 1H), 8.47 (d, 1H), 9.50 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750154B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-ef4469ed2e194530980c1f835209984c |
| Source note | uspto-grants-2010_07 |