3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole → HCID 12114963, compound

Participants

Reaction Conditions

Reaction Steps

To a solution of [(2R)-8-methoxy-2H-chromen-2-yl]methyl 4-methyl-benzenesulfonate (0.350 g, 1.01 mmol) in methyl sulfoxide (20 mL) was added 3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (0.601 g, 3.03 mmol) and the reaction mixture was heated to 80° C. for 12 h. The reaction mixture was allowed to cool to room temperature and was diluted with ethyl acetate (200 mL), washed with water (2×100 mL), aqueous sodium chloride (100 mL), dried (magnesium sulfate) and the solvent was removed in vacuo to give a crude solid. Purification by flash column chromatography (silica, methanol:ethyl acetate 1:9) followed by recrystallization from ethanol provided 0.218 g (58%, >97% ee) of 3-(1-{[(2R)-8-methoxy-2H-chromen-2-yl]methyl}-1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole as a yellow solid. [α]D25=+0.588 (c 10.21 in chloroform, >97% ee); Rf=0.43 (silica, methanol:ethyl acetate 1:9); mp 198-200° C. dec; Anal. Calcd. for C24H24N2O2.0.3 H2O: C, 76.29; H, 6.56; N, 7.41. Found: C, 76.02; H, 6.63; N, 7.43.

Provenance & Evidence