Diisopropylamine → HCID 23114727, compound

Under an argon atmosphere, n-butyl lithium (a 1.59M hexane solution, 76 ml, 121 mmol) was added to a tetrahydrofuran (400 ml) solution of diisopropylamine (17 ml, 121 mmol) at −70° C. The reaction mixture was stirred for 1 hour. To the reaction mixture was added dropwise a tetrahydrofuran (100 ml) solution of 2,5-dibromopyridine and the resulting mixture was stirred for 2 hours. To the reaction mixture was added dropwise 2,5-difluorobenzaldehyde (15 ml, 139 mmol) and the mixture was stirred for 1 hour. After addition of water, the resulting mixture was concentrated under reduced pressure. The residue thus obtained was extracted with dichloromethane. The organic layer thus obtained was dried over magnesium sulfate, and concentrated under reduced pressure. The residue thus obtained was washed with dichloromethane:hexane to yield a pale yellow powder. The filtrate was subjected to silica gel column chromatography. The fraction obtained from the hexane:ethyl acetate=6:1 eluate was concentrated under reduced pressure. The residue thus obtained and the above-described pale yellow powder were combined to give the title compound (18.4 g, 48.6 mmol, 52%) as a pale yellow powder.

1. stirringthe resulting mixture was stirred for 2 hours
2. stirringthe mixture was stirred for 1 hour
3. concentrationthe resulting mixture was concentrated under reduced pressure
4. customThe residue thus obtained
5. extractionwas extracted with dichloromethane
6. customThe organic layer thus obtained
7. dry with materialwas dried over magnesium sulfate
8. concentrationconcentrated under reduced pressure
9. customThe residue thus obtained
10. washwas washed with dichloromethane
11. customhexane to yield a pale yellow powder
12. concentrationethyl acetate=6:1 eluate was concentrated under reduced pressure
13. customThe residue thus obtained

ORD record

ord-5c84b1416c734c5b8c0d6df1adfb44f3

Source dataset

uspto-grants-2011_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07932271B2