Indole → 5-benzyloxy-6-isopropyl-3-methyl-1H-indole

The methylation carried out in this step follows the procedure for indole alkylation reported by Marino et al. in “The Enantioselective Synthesis of (−) Physostigmine Via Chiral Sulfoxides”, J. Am. Chem. Soc. (1992), 114, 5566-5572. 5-Benzyloxy-6-isopropyl-1H-indole (0.855 g, 3.22 mmol) was dissolved in 20 mL of dry THF, and the resulting solution was cooled in an ice bath. Ethyl magnesium bromide (4.9 ml, 4.9 mmol in ether) was added dropwise to the solution, and the solution was then stirred for 4 hours at room temperature. Methyl iodide (1.42 g, 10 mmol) was then added, and stirring was continued for an additional 18 hours at room temperature. The reaction mixture was poured into ice water and extracted with ethyl acetate. The combined organic layers were washed with saturated ammonium chloride, dried (MgSO4), and concentrated in vacuo. The resulting residue was purified with flash chromatography (ethyl acetate/hexanes=1/9) to yield 325 mg of 5-benzyloxy-6-isopropyl-3-methyl-1H-indole Mass Spec (M+H): 280.

1. temperaturethe resulting solution was cooled in an ice bath
2. stirringstirring
3. waitwas continued for an additional 18 hours at room temperature
4. extractionextracted with ethyl acetate
5. washThe combined organic layers were washed with saturated ammonium chloride
6. dry with materialdried (MgSO4)
7. concentrationconcentrated in vacuo
8. customThe resulting residue was purified with flash chromatography (ethyl acetate/hexanes=1/9)

ORD record

ord-93b3dbafa2b04c219c3783d18fab4ea7

Source dataset

uspto-grants-2010_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07858632B2