HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 86610970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 66919015 | HCID 66919015 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86610970 | HCID 86610970 | — |
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-{[2-(dimethylamino)ethyl]thio}-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.62 (m, 2H), 0.76 (m, 2H), 2.21 (s, 3H), 2.47 (s, 6H), 2.89 (d, 6), 2.93 (m, 1H), 3.37 (m, 2H), 3.52 (m, 2H), 7.60 (d, 1H), 7.84 (d, 1H), 7.90 (d, 1H), 7.99 (m, 2H), 8.20 (d, 1H), 8.40 (s, 1H), 8.52 (d, 1H), 9.58 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750154B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-b3279ddbb9994ef2bdbe35dd47de0f30 |
| Source note | uspto-grants-2010_07 |