Reacción #66060

ord-e785ea6338194dd69e22ecc6c663d32e

Ecuación de reacción

CCCOS(=O)(=O)c1ccc(C)cc1
propyl tosylate
Cc1ccc(S(=O)(=O)O)cc1
P-TSA
Rendimiento 50.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaUnder continuous stirring, the mixture was heated to a temperature of between 65° C. and 68° C
  2. 2
    workup.ADDITIONwas added slowly over a period of 2 hours
  3. 3
    workup.STIRRINGstirred for an additional 1 hour
  4. 4
    FiltraciónThe precipitated material was collected by filtration
  5. 5
    Lavadowashed with 7.32 L, MTBE
  6. 6
    Lavadoa wash with 9.2 L heptane
  7. 7
    OtroThe washed precipitated cake
  8. 8
    Otrowas dried under high vacuum at 30° C. to 35° C

Procedimiento

A 72 liter unjacketed reactor was charged with 1.84 kg (10.87 mol) of R(+)-2,6 diamino-4,5,6,7-tetrahydro-benzothiazole (R(+) diamine), followed by 14.7 L of dimethyl formamide (DMF). Under continuous stirring, the mixture was heated to a temperature of between 65° C. and 68° C. A solution of 2926 grams propyl tosylate and 1761 grams diisopropylethyleamine in 3.455 L DMF was added slowly over a period of 2 hours. The reaction was continued at 67° C. for an additional 4 hours, after which the solution was gradually cooled to room temperature (18° C. to 22° C.) and stirred for an additional 15 hours. The solution was diluted with 14.72 L of MTBE over a time period of 30 minutes, and stirred for an additional 1 hour. The precipitated material was collected by filtration and washed with 7.32 L, MTBE, followed by 3 washes of 3.68 L each of ethanol, and a wash with 9.2 L heptane. The washed precipitated cake was dried under high vacuum at 30° C. to 35° C. The final weight of the dried product was 2090 grams, representing a 50% yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524695B2uspto-grants-2013_09