Реакция #70794

ord-3cec4fd0a5274151a8e24be020b9b9fa

Уравнение реакции

COC(=O)c1cc(Br)cc2c1ccn2C(C)C
methyl 6-bromo-1-(1-methylethyl)-1H-indole-4-carboxylate
CS(=O)[O-].[Na+]
sodium methanesulfinate
CNCCNC
N,N′-dimethyl-1,2-ethanediamine
CC(C)n1ccc2c(C(=O)O)cc(S(C)(=O)=O)cc21
product
Выход 9.2%
CC(C)n1ccc2c(C(=O)O)cc(S(C)(=O)=O)cc21
1-Isopropyl-6-(methylsulfonyl)-1H-indole-4-carboxylic acid
Выход 9.2%

Растворители

Условия реакции

Температура
165°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe mixture was degassed for 5 min
  2. 2
    Другоеby bubbling N2
  3. 3
    workup.ADDITIONCopper(I) trifluoromethanesulfonate benzene complex (25.6 mg, 0.043 mmol) was added
  4. 4
    ФильтрацияThe mixture was filtered
  5. 5
    Другоеthe DMSO solution was purified

Методика

To a 10-mL microwave tube were added methyl 6-bromo-1-(1-methylethyl)-1H-indole-4-carboxylate (160 mg, 0.540 mmol), sodium methanesulfinate (80 mg, 0.702 mmol), DMSO (2 mL), and N,N′-dimethyl-1,2-ethanediamine (6.19 mg, 0.070 mmol), and the mixture was degassed for 5 min by bubbling N2. Copper(I) trifluoromethanesulfonate benzene complex (25.6 mg, 0.043 mmol) was added and the mixture was heated to 165° C. for 2 h with stirring. The mixture was filtered and the DMSO solution was purified using reverse-phase HPLC to give 14 mg of product as white solid. 1H NMR (400 MHz, DMSO-d6) ppm 1.51 (d, J=4.00 Hz, 6H), 4.90-5.11 (m, 1H), 7.13 (d, J=3.03 Hz, 1H), 7.98-8.08 (m, 1H), 8.15-8.23 (m, 1H), 8.32-8.46 (m, 1H), 13.19 (br. s., 1H). MS: (M+H)+=281.9.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08536179B2uspto-grants-2013_09