2-((2-((6-Bromohexyl)oxy)ethoxy)methyl)-1,3-dichlorobenzene → 6-{2-[(6-{2-[(2,6-Dichlorobenzyl)oxy]ethoxy}hexyl)amino]-1-hydroxyethyl}-2-(hydroxymethyl)pyridin-3-ol

온도

70 °C

A mixture of 2-amino-1-(2-phenyl-4H-[1,3]dioxino[5,4-b]pyridin-6-yl)ethanol (EP220054A2) (93 mg) and 2-({2-[(6-bromohexyl)oxy]ethoxy}methyl)-1,3-dichlorobenzene (98 mg) in dimethylformamide (1 ml) and diisopropylethylamine (0.2 ml) was heated to 70° C. for 4 h and then at 20° C. for 16 h. The mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and water. The organic phase was washed with water, brine, dried and evaporated to dryness. The residue was dissolved in ethanol and applied to an SCX-2 cartridge (10 g) eluting with ethanol, followed by 10% aqueous ammonia in ethanol. The ammoniacal fractions were concentrated under reduced pressure, and the residue was dissolved in acetic acid (5 ml) and water (2 ml) and the mixture was heated to 70° C. for 40 min. The solvent was removed under reduced pressure and the residue was purified by chromatography on a silica SPE cartridge (10 g) eluting with 10% aqueous ammonia in ethanol-dichloromethane (1:9 to 1:3). Appropriate fractions were combined and concentrated and the residue dissolved in acetic acid and re-evaporated to dryness to give the title compound (124 mg). LCMS RT=2.46 min, ES+ve m/z 487/489/491 (M+H)+.

1. concentrationThe mixture was concentrated under reduced pressure
2. customthe residue was partitioned between ethyl acetate and water
3. washThe organic phase was washed with water, brine
4. customdried
5. customevaporated to dryness
6. dissolutionThe residue was dissolved in ethanol
7. washeluting with ethanol
8. concentrationThe ammoniacal fractions were concentrated under reduced pressure
9. dissolutionthe residue was dissolved in acetic acid (5 ml)
10. temperaturewater (2 ml) and the mixture was heated to 70° C. for 40 min
11. customThe solvent was removed under reduced pressure
12. customthe residue was purified by chromatography on a silica SPE cartridge (10 g)
13. washeluting with 10% aqueous ammonia in ethanol-dichloromethane (1:9 to 1:3)
14. concentrationconcentrated
15. dissolutionthe residue dissolved in acetic acid
16. customre-evaporated to dryness

ORD 기록

ord-ffbdca865243405aaf70f10caeb2e3b6

출처 데이터셋

uspto-grants-2009_05

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07538127B2