Trifluoroacetic anhydride → 2-((5-Methoxy-1H-indol-6-yl)oxy)-N,N-dimethylethan-1-amine

A stirred solution of N-[3-(2-dimethylaminoethoxy)4-methoxyphenyl]aminoacetaldehyde dimethyl acetal (D12, 5.3 g, 0.018 mole) in trifluoroacetic acid (22 ml) at -5° C. under argon was treated dropwise over 40 minutes with trifluoroacetic anhydride (22 ml). After a further 30 minutes the dark solution was treated with more trifluoroacetic acid (33 ml) and then heated under reflux for 7 hours. The solution was concentrated in vacuo and the residue basified with 10% Na2CO3 solution and extracted with ethyl acetate. The extract was dried (Na2SO4), concentrated in vacuo and the residue dissolved in methanol (100 ml), treated with potassium carbonate (10 g) and stirred at room temperature for 3 hours. The mixture was concentrated in vacuo,.the residue treated with water (60 ml) and extracted with ethyl acetate (2×70 ml). The combined extract was dried (Na2SO4) and concentrated in vacuo to afford the title compound as a brown solid (3.5 g, 83%).

1. temperatureheated
2. temperatureunder reflux for 7 hours
3. concentrationThe solution was concentrated in vacuo
4. extractionextracted with ethyl acetate
5. dry with materialThe extract was dried (Na2SO4)
6. concentrationconcentrated in vacuo
7. dissolutionthe residue dissolved in methanol (100 ml)
8. additiontreated with potassium carbonate (10 g)
9. concentrationThe mixture was concentrated in vacuo,.the residue
10. additiontreated with water (60 ml)
11. extractionextracted with ethyl acetate (2×70 ml)
12. extractionThe combined extract
13. dry with materialwas dried (Na2SO4)
14. concentrationconcentrated in vacuo

ORD-Eintrag

ord-670d8d56d37444a1aff144c1f82bef7c

Quelldatensatz

uspto-grants-1998_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05817833