HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526274Generated: November 4, 2026
Methanesulfonic Acid → HCID 117666883, compound
https://huagongshe.com/reaction/1526274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 71667534 | HCID 71667534 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 117666883 | HCID 117666883 | — |
Reaction Steps
A mixture of 5-[3-(acryloylamino)phenoxy]-6-ethyl-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyrazine-2-carboxamide (100 mg) and acetonitrile (3 mL) was heated to 50° C., and a 2 M aqueous methanesulfonic acid solution (100 μl) was added thereto, followed by stirring at 50° C. for 30 minutes. After leaving to be cooled to room temperature, the mixture was stirred at room temperature for 15 hours. The precipitated solid was collected by filtration and dried at 50° C. for 6 hours under reduced pressure to obtain 5-[3-(acryloylamino)phenoxy]-6-ethyl-3-{[4-(4-methylpiperazin-1-yl)phenyl]amino}pyrazine-2-carboxamide monomethanesulfonate (104 mg) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09085540B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-517a0605088c47f48efba6a9ebce01bd |
|---|
| Source note | uspto-grants-2015_07 |
|---|