HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 178470718, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178470715 | HCID 178470715 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178470718 | HCID 178470718 | — |
Reaction Steps
To a stirred solution of 1-((S)-Nα -t-butoxycarbonyl-Nω -nitroarginyl)-4-(ethoxycarbonylmethyl)piperidine (1.2 g) in dichloromethane (25 ml) cooled to 0° to 5° C. is slowly added trifluoroacetic acid (2.8 g) and the reaction mixture is allowed to warm to room temperature and is then stirred for 6 hours. Toluene (30 ml) is then added and the mixture is concentrated by evaporation and then co-evaporated with further toluene portions (2×30 ml) and the eventual residue is triturated with ether, collected by filtration, washed with ether and dried to constant weight in vacuo to give 1-((S)-Nω -nitroarginyl)-4-(ethoxycarbonylmethyl)-piperidine trifluoroacetate as a white solid, Rf (BuOH/CH3COOH/H2O 3:2:1)=0.50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686564 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-927317931d6f48b39cf618f45ca8fa89 |
| Source note | uspto-grants-1997_11 |