HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 86610964, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 11751183 | HCID 11751183 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86610964 | HCID 86610964 | — |
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-(4-isopropylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.70 (m, 2H), 1.30 (d, 6H), 2.14 (s, 3H), 2.35 (s, 3H), 2.85 (m, 1H), 3.10-3.28 (m, 4H), 3.55 (m, 3H), 4.07 (m, 2H), 7.53 (d, 1H), 7.57 (s, 1H), 7.71 (m, 2H), 7.82 (s, 1H), 7.91 (d, 1H), 8.18 (s, 1H), 8.44 (d, 1H), 9.40 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750154B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-dab103ac53a540c2812c92419c5f74af |
| Source note | uspto-grants-2010_07 |