Diisobutylaluminum hydride → [3-Phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]methanol

To a stirred solution of 3-phenyl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid ethyl ester (3.24 g, 7.72 mmol) in toluene (40 mL) cooled to −78° C. and under a nitrogen atmosphere was added 1.0M DIBAL-H in toluene (23.2 mL, 23.2 mmol). The reaction mixture was stirred at −78° C. for 15 min and then at −10° C. for 30 min. After re-cooling to −78° C., the reaction mixture was quenched with water (20 mL) and then allowed to warm to RT. The mixture was partitioned between EtOAc and 1.0M HCl and the aqueous phase was extracted with additional EtOAc (×3). The combined organic layers were washed with water, then dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 30-100% DCM in pentane) affording [3-Phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]methanol as a white foam (2.49 g, 85%). LCMS: RT 4.77 min [M+Na]+ 400.1.

1. waitat −10° C. for 30 min
2. temperatureAfter re-cooling to −78° C.
3. customthe reaction mixture was quenched with water (20 mL)
4. temperatureto warm to RT
5. customThe mixture was partitioned between EtOAc and 1.0M HCl
6. extractionthe aqueous phase was extracted with additional EtOAc (×3)
7. washThe combined organic layers were washed with water
8. dry with materialdried (Na2SO4)
9. concentrationconcentrated in vacuo
10. customThe resulting residue was purified by column chromatography (Si—PCC, gradient 30-100% DCM in pentane)

ORD-Eintrag

ord-050e22efc04f470a85222958940614ed

Quelldatensatz

uspto-grants-2014_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08653089B2