Diisopropylamine → HCID 23114659, compound

Under an argon atmosphere, n-butyl lithium (a 1.58M hexane solution, 88 ml, 138 mmol) was added to a tetrahydrofuran (200 ml) solution of diisopropylamine (21 ml, 150 mmol) at −78° C. The resulting mixture was stirred for 1 hour. To the reaction mixture was added dropwise a tetrahydrofuran (100 ml) solution of 2-bromo-5-chloropyridine (19 g, 98.7 mmol). The resulting mixture was stirred for 1.5 hours. To the reaction mixture was added dropwise 2,5-difluorobenzaldehyde (16 ml, 148 mmol), followed by stirring for 2 hours. After addition of water, the resulting mixture was concentrated under reduced pressure. The residue was extracted with dichloromethane. The organic layer thus obtained was dried over magnesium sulfate, and concentrated under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography. The fraction obtained from the hexane:ethyl acetate=6:1 eluate was concentrated under reduced pressure to give the title compound (24.8 g, 74.1 mmol, 75%) as a pale yellow powder.

1. stirringThe resulting mixture was stirred for 1.5 hours
2. stirringby stirring for 2 hours
3. concentrationthe resulting mixture was concentrated under reduced pressure
4. extractionThe residue was extracted with dichloromethane
5. customThe organic layer thus obtained
6. dry with materialwas dried over magnesium sulfate
7. concentrationconcentrated under reduced pressure
8. customThe residue thus obtained
9. concentrationethyl acetate=6:1 eluate was concentrated under reduced pressure

ORD record

ord-d1e710bfcdbd40b2934e20cdf1924a25

Source dataset

uspto-grants-2011_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07932271B2