HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Dimethylaminopyridine → HCID 70092293, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | t-Butoxycarbonyltryptophan fluoride | HCID 10979687 | — |
| Reactant | N-butanesulfonyl-N-trimethylsilylamide | HCID 86751785 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70092293 | HCID 70092293 | — |
Reaction Steps
A solution of N-butanesulfonyl-N-trimethylsilylamide (0.75 g, 3.6 mmol), t-butoxycarbonyltryptophan fluoride (0.92 g, 3.01 mmol), and dimethylaminopyridine (37 mg, 0.3 mmol) in tetrahydrofuran (10 ml) is stirred at room temperature for 2 hours. The mixture is diluted with 10% citric acid and extracted with ethyl acetate. The organic layer is washed with water and brine, dried over magnesium sulfate, and concentrated in vacuo. The crude material is chromatographed on silica gel with ethyl acetate/hexane (1:1) and trace of acetic acid to give N-butanesulfonyl-(t-butoxycarbonyl)tryptophanamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05703106 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-21ac40b472934c85b3b1f9128507e183 |
| Source note | uspto-grants-1997_12 |