Reacción #2254154

ord-8cd3830461cc476896c7180c97132376

Ecuación de reacción

CC(C)[S+](N)C(C)C.Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1
S,S-Diisopropyl-S-aminosulfonium 2,4,6-trimethyl-phenylsulfonate
O=c1[nH]c2c(Cl)cc(Cl)cc2c(=O)o1
6,8-dichloro-1H-benzo[d][1,3]oxazine-2,4-dione
O
Water
CC(C)(C)[O-].[K+]
potassium tert-butanolate
CC(C)S(=NC(=O)c1cc(Cl)cc(Cl)c1N)C(C)C
title compound
CC(C)S(=NC(=O)c1cc(Cl)cc(Cl)c1N)C(C)C
2-amino-N-(bis-2-propyl-λ4-sulfanylidene)-3,5-dichloro-benzamide

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto come to room temperature
  2. 2
    Otrothe organic phase was separated
  3. 3
    Extracciónthe aqueous phase further extracted with methylene chloride (2×100 mL)
  4. 4
    SecadoThe combined organic extracts were dried (MgSO4)
  5. 5
    Concentraciónconcentrated in vacuo

Procedimiento

To a suspension of 6,8-dichloro-1H-benzo[d][1,3]oxazine-2,4-dione (45.0 g, 70.7 mmol) in methylene chloride (500 mL) was added S,S-Diisopropyl-S-aminosulfonium 2,4,6-trimethyl-phenylsulfonate (77.6 g, 234 mmol). The reaction mixture was cooled to 0° C. and potassium tert-butanolate (8.73 g, 77.8 mmol) was added after which the reaction was allowed to come to room temperature and stirred for 16 h. Water (200 mL) and methylene chloride (50 mL) were then added, the organic phase was separated and the aqueous phase further extracted with methylene chloride (2×100 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo to afford the title compound (62.8 g, quant.).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09044016B2uspto-grants-2015_06