反应详情

温度

100 °C

Compound 464A (15.0 g, 59.3 mmol) was dissolved in DMF (120 mL) and zinc cyanide (4.20 g, 35.9 mmol) was added. Bis(diphenylphosphino)ferrocene (3.00 g, 5.40 mmol) and tris(benzylidineacetone)dipalladium (3.00 g, 3.30 mmol) were then added and the reaction was heated to 100° C. for 1.5 h. The reaction was cooled to 22° C. and then poured into concentrated ammonium hydroxide (900 mL) resulting in an orange precipitate which was filtered and rinsed with cold water (1 L). The resulting precipitate was dissolved in methylene chloride, washed with brine (1×300 mL) and then dried over anhydrous sodium sulfate. Concentration in vacuo gave the crude material as an orange solid which was purified by flash chromatography on silica gel eluting with methylene chloride to give 6.01 g (51%) of compound 464B as a yellow solid. HPLC: 99% at 1.900 min (retention time) (YMC S5 ODS column, 4.6×50 mm, eluting with 10–90% aqueous methanol over 4 min containing 0.2% phosphoric acid, 4 ml/min, monitoring at 220 nm).

1. temperatureThe reaction was cooled to 22° C.
2. customresulting in an orange precipitate which
3. filtrationwas filtered
4. washrinsed with cold water (1 L)
5. dissolutionThe resulting precipitate was dissolved in methylene chloride
6. washwashed with brine (1×300 mL)
7. dry with materialdried over anhydrous sodium sulfate
8. concentrationConcentration in vacuo
9. customgave the crude material as an orange solid which
10. customwas purified by flash chromatography on silica gel eluting with methylene chloride