HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Fmoc-d-methionyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | (2R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylsulfanyl)butanoic acid | HCID 6992521 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Fmoc-d-methionyl fluoride | HCID 23544816 | — |
Reaction Steps
FMOC-D-Methionine (5.00 g, 13.46 mmol) (Bachem) was dissolved in dichloromethane (70 mL). Pyridine (1.09 mL, 13.46 mmol) (Aldrich) and cyanuric fluoride (1.82 g, 13.46 mmol) (Aldrich) were successively added at room temperature and the mixture was stirred for 4 hours. Ice cold water (100 mL) was added and the resulting slurry was filtered. The filtrate was poured into a separatory funnel and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford FMOC-D-methionyl fluoride as a white powder. (Yield 3.7 g., 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084270B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-ff701405dbdb4c8d96cc24948af218ae |
| Source note | uspto-grants-2006_08 |