HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 69424678, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Dichlorobenzenesulfonyl chloride | HCID 522388 | — |
| Reactant | HCID 58638720 | HCID 58638720 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69424678 | HCID 69424678 | — |
Reaction Steps
6.88 μl (65.77 μmol) of diisopropylethylamine and a solution of 3.26 mg (13.15 μmol) of 3,5-dichlorobenzenesulphonyl chloride in 150 μl of acetonitrile were added to a solution of 7.3 mg (13.15 μmol) of tert.-butyl 2-(4-{2-[methyl-(3-methylaminopropionyl)amino]ethyl}phenyl)-4,5-dihydroimidazole-1-carboxylate in 100 μl of acetonitrile. The reaction mixture was stirred at room temperature for 1.5 hours. 500 μl of a solution of trifluoroacetic acid and water (95/5) were then added, and the mixture was stirred at room temperature for a further 30 min. The reaction mixture was then evaporated to dryness in a Christ-Speedvac. The crude product obtained in this manner was purified by HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291642B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-7ad65b91f9064dc186196a345e014eba |
| Source note | uspto-grants-2007_11 |