Reacción #3863

ord-649ea945dd7e4b54ae14924d504966d6

Ecuación de reacción

C1CCNCC1
Piperidine
CS(=O)(=O)Cl
Methane sulfonyl chloride
COc1ccc2c(c1)C(O)CCO2
product
COc1ccc2c(c1)C(O)CCO2
6-Methoxy-4-hydroxy-2,3-dihydrobenzopyran
O=C([O-])O.[Na+]
sodium bicarbonate
COc1ccc2c(c1)C(N1CCCCC1)CCO2
desired product
COc1ccc2c(c1)C(N1CCCCC1)CCO2
6-Methoxy-4-piperidino-2,3-dihydrobenzopyran

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to 0° C
  2. 2
    workup.STIRRINGthe solution stirred at RT overnight
  3. 3
    workup.STIRRINGthe mixture is stirred for 30 minutes
  4. 4
    OtroThe organic layer is separated
  5. 5
    Lavadowashed with sat'd NaCl
  6. 6
    Otrodried
  7. 7
    FiltraciónThe solution is filtered
  8. 8
    Otrothe filtrate evaporated in vacuo

Procedimiento

Methane sulfonyl chloride (14.9 ml) is added dropwise to a stirred solution of the product obtained in Step 1. (31.6 g) and triethylamine (29.3 ml) in methylene chloride (750 ml) cooled to 0° C. under nitrogen. The reaction mixture is stirred at RT for 21/2 hours and cooled to 0° C. Piperidine (175 ml) is added to the cooled reaction mixture and the solution stirred at RT overnight. Sat'd aq. sodium bicarbonate is added to the solution and the mixture is stirred for 30 minutes. The organic layer is separated, washed with sat'd NaCl and dried. The solution is filtered and the filtrate evaporated in vacuo yielding the desired product as its hydrochloride salt.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04722925uspto-grants-1988_02