Reaktion #6843

ord-b5ef23cd1e7d40e5b80f3c58363f7221

Reaktionsgleichung

CI
iodomethane
c1ccc2[nH]ccc2c1
indole
CC(C)[Si](Oc1ccc2[nH]c3c(c2c1)CCN(C(=O)OC(C)(C)C)C3)(C(C)C)C(C)C
6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester
CC(C)(C)[O-].[K+]
potassium tert-butoxide
C1COCCOCCOCCOCCOCCO1
18-crown-6
CC(C)[Si](Oc1ccc2c(c1)c1c(n2C)CN(C(=O)OC(C)(C)C)CC1)(C(C)C)C(C)C
9-methyl-6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester
Ausbeute 41.9%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solids were removed by filtration
  2. 2
    Sonstigethe solvent was evaporated

Vorschrift

A solution of 6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester (175 mg, 0.39 mmol) in 3 mL of ethyl ether was added to a vigorously stirring solution of potassium tert-butoxide (263 mg) and 18-crown-6 (16 mg) in 10 mL ethyl ether. After 10 min, iodomethane (73 uL) in 0.5 mL of ethyl ether was added to the indole solution and the resulting mixture was stirred for 2 h. The solids were removed by filtration and the solvent was evaporated. Silica gel chromatography (10% ethyl acetate in hexanes) gave 9-methyl-6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester (75 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084154B2uspto-grants-2006_08