Chloroform → 5-Fluoro-3-(2-(pyrrolidin-1-yl)ethyl)-1H-indole

Temperature

70 °C

Pyrrolidine (2.94 g, 3.4 ml, 41.3 mmol) was dissolved in abs dioxane (100 ml), 3-(2-bromo-ethyl)-5-fluoro-1H-indole (5.00 g, 20.7 mmol) was added at RT and the mixture was stirred at 70° C. for 8 h. The solution was concentrated, the residue was taken up in CHCl3 (150 ml) and the mixture was washed with water (2×50 ml). The organic phase was dried over Na2SO4, filtered and concentrated i. vac. The residue obtained was purified by flash chromatography with 500 g of silica gel and chloroform/methanol (20:1→9:1→4:1→methanol. Only with methanol was a salt of the compound obtained, and it was then possible to liberate this by stirring with 2N NaOH and CHCl3. The phases were separated, the aqueous phase was extracted twice with CHCl3 and the combined organic phases were dried over Na2SO4, filtered and concentrated i. vac. The chloroform used was probably contaminated with HCl.

1. concentrationThe solution was concentrated
2. washthe mixture was washed with water (2×50 ml)
3. dry with materialThe organic phase was dried over Na2SO4
4. filtrationfiltered
5. concentrationconcentrated i
6. customThe residue obtained
7. customwas purified by flash chromatography with 500 g of silica gel and chloroform/methanol (20:1→9:1→4:1→methanol
8. customobtained
9. customThe phases were separated
10. extractionthe aqueous phase was extracted twice with CHCl3
11. dry with materialthe combined organic phases were dried over Na2SO4
12. filtrationfiltered
13. concentrationconcentrated i

ORD record

ord-661c04de31d14ae4b3a2897e9c378f23

Source dataset

uspto-grants-2012_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08138187B2