Reacción #9426

ord-b2ba3a136dae496caa6ed5d95948979f

Ecuación de reacción

CCC1(CC)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
5-(3-chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
Lawesson's reagent
CCC1(CC)C(=S)Nc2ccc(-c3cccc(Cl)c3)cc21
title compound
CCC1(CC)C(=S)Nc2ccc(-c3cccc(Cl)c3)cc21
5-(3-CHLOROPHENYL)-3,3-DIETHYL-1,3-DIHYDRO-2H-INDOLE-2-THIONE

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux

Procedimiento

The title compound was prepared from 5-(3-chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one compound (100 mg) and Lawesson's reagent (100 mg) in toluene (10 ml) at reflux, according to General Procedure A, to afford the product (0.023 g) as a yellow solid: 1H NMR (DMSO-d6) δ 12.73 (br s, 1H), 7.77 (t, 1H, J=1.8 Hz), 7.75 (d, 1H, J=1.6 Hz), 7.68–7.62 (m, 2H), 7.48 (t, 1H, J=7.9 Hz), 7.40 (d, 1H, J=8.3 Hz), 7.09 (d, 1H, J=8.1 Hz), 2.07–2.00 (m, 2H), 1.86–1.79 (m, 2H) and 0.37 (t, 6H, J=7.3 Hz): MS ((−)-APCI) m/z 314/316 [M−H]−.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091234B2uspto-grants-2006_08