تفاعل #2048331

ord-8d4a91fb40c8495cb54e71a41139c486

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 by column chromatography (10-50% EtOAc in hexanes

الإجراء التجريبي

A solution of methyl 5-ethyl-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylate (1 g, 3.99 mmol)[prepared in Example 98] and N-bromosuccinimide (0.711 g, 3.99 mmol) in tetrahydrofuran (8 ml) was stirred in a sealed tube for 1 h at 70° C. 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 by column chromatography (10-50% EtOAc in hexanes yielding methyl 4-(4-bromo-1-methyl-1H-pyrazol-5-yl)-5-ethyl-2-thiophenecarboxylate (1.2 g, 3.54 mmol, 89% yield) as an orange oil: LCMS (ES) m/e 329, 331 (M, M+2)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08410158B2uspto-grants-2013_04