تفاعل #1932667

ord-a3778127d936435b9db857b5d6d26d79

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was then 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
    أخرىthen purified via column chromatography (silica, 10-40% EtOAC in hexanes)

الإجراء التجريبي

A solution of methyl 5-ethyl-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate (980 mg, 3.92 mmol) [prepared in Example 98] and N-bromosuccinimide (697 mg, 3.92 mmol) in tetrahydrofuran (19.6 ml) was stirred in a sealed tube for 1 h at 70° C. The reaction mixture was then partitioned between H2O-DCM and the aqueous phase was washed several times with DCM. The combined organic fractions were dried over Na2SO4, concentrated then purified via column chromatography (silica, 10-40% EtOAC in hexanes) yielding methyl 4-(4-bromo-1-methyl-1H-pyrazol-5-yl)-5-ethyl-2-thiophenecarboxylate (1.1 g, 3.34 mmol, 85% yield) as a yellow oil: LCMS (ES) m/e 329, 331 (M, M+2)+.

المصدر

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