Pyridine → HCID 11148207, compound

Temperature

-15 °C

To an oven-dried, septaed 10 mL round-bottom flask, cooled under an argon atmosphere, and charged with (R)-N-BOC-alanine, 24b, (189.2 mg, 1.00 nmmol) was added 2.5 mL freshly distilled CH2Cl2 under argon. The reaction was cooled to −15 C and to the flask was added cyanuric fluoride (450 μL, 5 mmol). The reaction was stirred at −15° C. for 15 minutes then anhydrous pyridine (81 μL, 1.0 mmol) was added. Stirring was maintained at −15° C. for 90 minutes, with reaction progress indicated by the gradual formation of a precipitate. Without warming, the crude reaction was poured over ice, and immediately extracted twice with CH2Cl2. The combined CH2Cl2 extracts were washed once with water, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The resulting colorless oil was dissolved in CH2Cl2, and precipitated with hexane to afford 155.1 mg of a mixture of 24b and 25b as white crystals. FTIR (film) 1842 cm−1.

1. temperaturecooled under an argon atmosphere
2. temperatureThe reaction was cooled to −15 C and to the flask
3. stirringStirring
4. temperaturewas maintained at −15° C. for 90 minutes, with reaction progress
5. temperatureWithout warming
6. customthe crude reaction
7. additionwas poured over ice
8. extractionimmediately extracted twice with CH2Cl2
9. washThe combined CH2Cl2 extracts were washed once with water
10. dry with materialdried over anhydrous magnesium sulfate
11. filtrationfiltered
12. concentrationconcentrated in vacuo
13. dissolutionThe resulting colorless oil was dissolved in CH2Cl2
14. customprecipitated with hexane

ORD record

ord-542ab548b617458184000781e10e441b

Source dataset

uspto-grants-2006_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07045360B2