HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → n-Cyclopropyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3(4h)-yl]benzamide bismethanesulfonate salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Azd-6703 | HCID 11373432 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | n-Cyclopropyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3(4h)-yl]benzamide bismethanesulfonate salt | HCID 86610969 | — |
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-4-methyl-3-[6-(4 methylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.70 (m, 2H), 2.13 (s, 1H), 2.40 (s, 6H), 2.87 (m, 1H), 2.89 (d, 3H), 3.10-3.30 (m, 4H), 3.58 (m, 2H), 4.05 (m, 2H), 7.52 (d, 1H), 7.59 (d, 1H), 7.71 (m, 2H), 7.84 (s, 1H), 7.91 (m, 1H), 8.22 (s, 1H), 8.47 (d, 1H), 9.74 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750154B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-8ce1c4862fdf41dbb34a8d4a8f7be47e |
| Source note | uspto-grants-2010_07 |