Reacción #80133

ord-95294ab135c34daba87c459d9f90d4e2

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe organic phase was separated
  2. 2
    Lavadowashed with brine
  3. 3
    Secadodried over sodium sulfate
  4. 4
    Concentraciónconcentrated in vacuo

Procedimiento

To a stirred solution of 23.6 g (131 mmol) 2-amino-4-methoxybenzothiazole and 12.6 ml (157 mmol) pyridine in 230 ml dichloromethane at 0° C. was added dropwise 10.6 ml (137 mmol) methyl chloroformate and stirring continued for 1 hour. The mixture was then poured onto 1 M hydrochloric acid and the organic phase was separated, washed with brine, dried over sodium sulfate, and concentrated in vacuo to afford 31.0 g (99%) (4-methoxy-benzothiazol-2-yl)-carbamic acid methyl ester as a white solid. ES-MS m/e (%): 239 (M+H+, 100).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06713499B2uspto-grants-2004_03