Water → 2-[2-Methyl-3-(4-trifluoromethyl-phenyl)-benzo[b]thiophen-6-yloxy]-ethylamine

0.230 g (0.610 mmol) 6-(2-Azido-ethoxy)-2-methyl-3-(4-trifluoromethyl-phenyl)-benzo[b]thiophene and 0.484 g (1.83 mmol) of triphenylphosphin were dissolved in 1.6 ml of tetrahydrofuran. After stirring of the reaction mixture for 15 minutes at room temperature, 0.1 ml of water were added and the reaction mixture heated to 60° C. for 16 hours. It was then evaporated under reduced pressure, poured into 50 ml of water and extracted 3 times with 10 ml of dichloromethane. The combined dichloromethane phases were washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue formed was chromatographed on silica gel with a 9:1 v/v mixture of dichloromethane and methanol as the eluent giving 0.200 g (93.4%) 2-[2-Methyl-3-(4-trifluoromethyl-phenyl)-benzo[b]thiophen-6-yloxy]-ethylamine as colorless oil, MS: 352 (MH+).

1. temperaturethe reaction mixture heated to 60° C. for 16 hours
2. customIt was then evaporated under reduced pressure
3. additionpoured into 50 ml of water
4. extractionextracted 3 times with 10 ml of dichloromethane
5. washThe combined dichloromethane phases were washed with brine
6. dry with materialdried over magnesium sulfate
7. customevaporated under reduced pressure
8. customThe residue formed
9. customwas chromatographed on silica gel with a 9:1 v/v mixture of dichloromethane and methanol as the eluent

ORD-Eintrag

ord-2a66d6e7731a462a8e33a25aefc0463b

Quelldatensatz

uspto-grants-2008_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07449483B2