Diisopropylamine → HCID 69220534、化合物

温度

-78 °C

To a solution of 2.14 mL (15.3 mmol) of N,N-diisopropylamine in 50 mL of tetrahydrofuran at −78° C. was added 7.96 mL (15.6 mmol, 2.5M in hexane) of n-butyl lithium and the mixture was stirred at −78° C. for 10 min. The reaction was warmed to 0° C. and stirred at 0° C. for 15 min. The mixture was cooled down to −78° C. again, and a solution 2.50 g (11.7 mmol) of tert-butyl 2-methyl-3-oxopiperidine-1-carboxylate (Step C) in 5 mL of tetrahydrofuran was added to the mixture slowly. The mixture was stirred at −78° C. for 1 h. Then 1.77 mL (14.9 mmol) of trans-cinnamaldehyde in 5 mL of tetrahydrofuran (pre-cooled to −78° C.) was added to the reaction mixture and the reaction was stirred at −78° C. for 5 h. The reaction was quenched with saturated aqueous sodium bicarbonate solution and extracted with three portions of ether. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated. Purification by flash chromatography on a Biotage® system (silica gel, eluting with 10% ethyl acetate/hexane to 30% ethyl acetate/hexane) gave the tide compound. LC/MS 368 (M+23).

1. temperatureThe reaction was warmed to 0° C.
2. stirringstirred at 0° C. for 15 min
3. temperatureThe mixture was cooled down to −78° C. again
4. stirringThe mixture was stirred at −78° C. for 1 h
5. stirringthe reaction was stirred at −78° C. for 5 h
6. customThe reaction was quenched with saturated aqueous sodium bicarbonate solution
7. extractionextracted with three portions of ether
8. washThe combined organic layers were washed with brine
9. dry with materialdried over magnesium sulfate
10. concentrationconcentrated
11. customPurification by flash chromatography
12. washon a Biotage® system (silica gel, eluting with 10% ethyl acetate/hexane to 30% ethyl acetate/hexane)
13. customgave the tide compound

ORDレコード

ord-0240134dc6b2424cab84a7598461fb81

出典データセット

uspto-grants-2008_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07388019B2