反应 #43516

ord-e00a7c67eda048cfa266d1f33c8a8c27

反应方程式

CC(C)[Si](Sc1ccccc1C1CCN(C(=O)OC(C)(C)C)CC1)(C(C)C)C(C)C
4-(2-tri-iso-propylsilanylsulfanyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester
FC(F)(F)c1ccc(I)cc1
1-iodo-4-trifluoromethyl-benzene
CC(C)(C)[O-].[K+]
potassium tert-butoxide
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
tetra-n-butyl ammonium fluoride
CC(C)(C)OC(=O)N1CCC(c2ccccc2Sc2ccc(C(F)(F)F)cc2)CC1
4-[2-(4-trifluoromethyl-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester
收率 59.2%

反应条件

温度
110°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISSOLUTIONwas dissolved
  2. 2
    其他in dry
  3. 3
    其他degassed toluene (0.3 mL)
  4. 4
    workup.DISSOLUTIONPd2dba3 (1 mg) and DPEphos (1 mg) dissolved in dry toluene (0.2 mL)
  5. 5
    workup.ADDITIONwere added
  6. 6
    过滤The solution was filtered
  7. 7
    其他the solvent was evaporated off
  8. 8
    其他The crude product was purified by chromatography on silica gel (eluent

实验过程

A mixture of 4-(2-tri-iso-propylsilanylsulfanyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (38 mg, 0.085 mmol) and 1-iodo-4-trifluoromethyl-benzene (23 mg, 0.085 mmol) was dissolved in dry degassed toluene (0.3 mL). Pd2dba3 (1 mg) and DPEphos (1 mg) dissolved in dry toluene (0.2 mL) were added. To this solution were added potassium tert-butoxide (10 mg) and tetra-n-butyl ammonium fluoride (TBAF, 1M in TBF, 0.1 mL, 0.1 mmol) and the reaction mixture was stirred at 110° C. for 1 h under argon. The solution was filtered and the solvent was evaporated off. The crude product was purified by chromatography on silica gel (eluent: An increasing amount (0-100%) of ethyl acetate in heptane) to produce 4-[2-(4-trifluoromethyl-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester (3a1) as a clear oil (22 mg, 59% yield). This material was dissolved in methanol (1 mL) and hydrogen chloride in diethyl ether (2M, 1 mL) was added and the solution was stirred overnight at rt. The solvent was evaporated of and the crude product was purified by BPLC (containing 0.1% TFA in the standard eluent) to produce 4-[2-(4-trifluoromethyl-phenylsulfanyl)-phenyl]-piperidine 3a1 as the trifluoro-acetic acid salt. Yield: 3.2 mg (8% overall). LC/TOF (m/z) 338.0 (MH+); RT=2.29 min; purity (UV, ELSD): 98.3%, 97.1%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07732463B2uspto-grants-2010_06