HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 22009480, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 9874780 | HCID 9874780 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22009480 | HCID 22009480 | — |
Reaction Steps
Combine 1-(3,4,5-trimethoxybenzyl)-3-(2-(4-(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl-amino)piperidin-1-yl)ethyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine (0.53 g, 0.74 mmol) and methanesulfonic acid (0.15 g, 1.6 mmol) in ethyl acetate. Heat to reflux. After 1 hour, allow to cool to ambient temperature to form a solid. Decant the supernatant and add diethyl ether and stir. Twice more decant the supernatant and add diethyl ether. Decant the supernatant and evaporate in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211199B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-8b503ed5a08d4de98339402d0a16906a |
| Source note | uspto-grants-2001_04 |