Réaction #685015

ord-e5c64cb1b0074190b3bfe3616d9261b0

Équation de réaction

C1CC2(CCN1)OCCO2
1,4-dioxa-8-azaspiro[4,5]decane
CCN(CC)CC
Et3N
Cc1ccc(F)cc1S(=O)(=O)Cl
5-fluoro-2-methylbenzenesulfonyl chloride
Cc1ccc(F)cc1S(=O)(=O)N1CCC2(CC1)OCCO2
product
Rendement 100.2%
Cc1ccc(F)cc1S(=O)(=O)N1CCC2(CC1)OCCO2
8-(5-Fluoro-2-methylphenylsulfonyl)-1,4-dioxa-8-azaspiro[4.5]decane
Rendement 100.2%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrecold bath was removed
  2. 2
    workup.WAITAfter 15 h at room temperature
  3. 3
    workup.ADDITIONthe reaction mixture was diluted with ether (200 mL)
  4. 4
    Lavagewashed with 1N aq. HCl (2×50 mL), brine (50 mL)
  5. 5
    Séchagedried (Na2SO4)
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated

Mode opératoire

A stirred solution of 1,4-dioxa-8-azaspiro[4,5]decane (10.73 g, 75 mmol) and Et3N (8 mL, 57 mmol) in THF (150 mL) was cooled in an ice-water bath. To this mixture was slowly added 5-fluoro-2-methylbenzenesulfonyl chloride (10.5 g, 50.33 mmol) and stirred for 1 h and then cold bath was removed. After 15 h at room temperature, the reaction mixture was diluted with ether (200 mL), washed with 1N aq. HCl (2×50 mL), brine (50 mL), dried (Na2SO4), filtered and concentrated to give product as an off-white solid 15.9 g, 100%). 1H NMR (500 MHz, CDCl3) δ: 7.61 (1H, dd, J=8.6, 2.8 Hz), 7.28-7.26 (1H, m), 7.15 (1H, td, J=8.1, 2.8 Hz), 3.94 (4H, s), 3.35-3.32 (4H, m), 2.57 (3H, s), 1.78-1.76 (4H, m). HRMS (M+H) calcd for C14H19FNO4S: 316.1019; found: 316.1013.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07897593B2uspto-grants-2011_03