تفاعل #1932683

ord-afacd8133ecd4affa18ea5a9d96542d4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was partitioned between H2O-DCM
  2. 2
    غسيلthe aqueous phase was washed several times with DCM
  3. 3
    تجفيفThe combined organic fractions were dried over Na2SO4
  4. 4
    تركيزconcentrated
  5. 5
    أخرىpurified via column chromatography (10-50% EtOAc in hexanes)

الإجراء التجريبي

A solution of methyl 4-(4-bromo-1-methyl-1H-pyrazol-5-yl)-5-propyl-2-thiophenecarboxylate (242 mg, 0.71 mmol). PdCl2(dppf) (52 mg, 0.07 mmol), potassium carbonate (487 mg, 3.53 mmol) and trimethylboroxine (0.20 ml, 1.41 mmol) in N,N-Dimethylformamide (3.5 ml) was stirred at 110° C. in a sealed tube for 2 h. The reaction mixture was partitioned between H2O-DCM and the aqueous phase was washed several times with DCM. The combined organic fractions were dried over Na2SO4, concentrated and purified via column chromatography (10-50% EtOAc in hexanes) affording methyl 4-(1,4-dimethyl-1H-pyrazol-5-yl)-5-propyl-2-thiophenecarboxylate (184 mg, 0.60 mmol, 84° A yield) as a yellow oil: LCMS (ES) m/z=279 (M+H)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08946278B2uspto-grants-2015_02