HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1-(3,4,5-Trimethoxybenzyl)-3-(3-(4-(1h-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine methanesulfonic acid salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1-(3,4,5-trimethoxybenzyl)-3-(3-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine | HCID 9895457 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3,4,5-Trimethoxybenzyl)-3-(3-(4-(1h-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine methanesulfonic acid salt | HCID 22009175 | — |
Reaction Steps
Combine 1-(3,4,5-trimethoxybenzyl)-3-(3-(4-(1H-benzimidazol-2-yl-amino)piperidin-1-yl)propyl)-3-(4-fluorophenylmethyl)-2-oxopyrrolidine (0.37 g, 0.56 mmol) and methanesulfonic acid (0.17 g, 1.8 mmol) in ethyl acetate (10 mL). Heat to reflux. After 1 hour, cool to ambient temperature, add diethyl ether (75 mL). After 12 hours, evaporate the solvent to give a residue. Triturate the residue with diethyl ether (80 mL) to give a solid. Collect the solid and dry 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-84938087964e4fd7b8ba0437d9c481a7 |
| Source note | uspto-grants-2001_04 |