Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10751345 | HCID 10751345 | 91.8% |
Reaction Steps
To an oven-dried, septaed 25 mL round-bottom flask, cooled under an argon atmosphere, and charged with (S)-N-BOC-valine (217.2 mg, 1.00 mmol) was added 2.5 mL CH2Cl2, and pyridine (81 μL, 1.00 mmol). The solution was cooled to −15° C., and to the reaction was added cyanuric fluoride (450 μL, 5.0 mmol). The reaction was stirred at −15° C. for 60 minutes, with the gradual formation of a white precipitate. Without warming, the crude reaction was poured over ice, and immediately extracted twice with CH2Cl2. The combined CH2Cl2 extracts were washed once with ice-cold water, dried over anhydrous magnesium sulfate, and concentrated in vacuo to afford 201.3 mg of 25g as white needles. FTIR (neat) 1847 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07045360B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-102e6dc772de4f7682d52631ca2e19f6 |
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| Source note | uspto-grants-2006_05 |
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