Reacción #1531956

ord-d963380559a442ea9a4521d29c994e4f

Ecuación de reacción

CCOC(C)=O
ethyl acetate
O=[N+]([O-])c1cc(CCl)cc([N+](=O)[O-])c1
3,5-Dinitrobenzyl chloride
CC1=Nc2ccc(CC(=O)O)cc2C1(C)C
2,3,3-trimethyl-3H-indol-5-yl-acetic acid
[Br-].[Na+]
sodium bromide
O=C(O)Cc1ccc2c(c1)CC=[N+]2Cc1cc([N+](=O)[O-])cc([N+](=O)[O-])c1.[Br-]
solid
Rendimiento 54.0%
O=C(O)Cc1ccc2c(c1)CC=[N+]2Cc1cc([N+](=O)[O-])cc([N+](=O)[O-])c1.[Br-]
1-(3,5-dinitrobenzyl)-5-(carboxymethyl)-3H-indolium Bromide
Rendimiento 54.0%

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to room temperature
  2. 2
    OtroThe crude reaction mixture
  3. 3
    Filtraciónthe dark brown solid was filtered OFF
  4. 4
    workup.DISSOLUTIONdissolved in dimethylsulfoxide before purification by reverse phase chromatography

Procedimiento

3,5-Dinitrobenzyl chloride (12.46 g, 57.5 mmol) was added to a solution of 2,3,3-trimethyl-3H-indol-5-yl-acetic acid (2.5 g, 11.5 mmol) with sodium bromide (5.92 g, 57.5 mmol) in sulfolan (10 ml). The reaction was heated at 100° C. for 20 hrs, then cooled to room temperature. The crude reaction mixture was added dropwise to an excess of ethyl acetate and the dark brown solid was filtered OFF and dissolved in dimethylsulfoxide before purification by reverse phase chromatography. The product was isolated as beige solid (54% yield). 1H NMR (d6-DMSO): δH: 8.75 (s, 1H), 8.45 (s, 2H), 7.15 (s, 1H), 6.95 (d, 1H), 6.70 (d, 2H), 5.10 (s, 2H), 3.95 (s, 2H), 3.45 (s, 3H), 1.40 (s, 6H). MALDI-TOF, m/z=398 (M+=398 for C20H20N3O6).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07662973B2uspto-grants-2010_02