تفاعل #61688

ord-94c38d12c62f4e1893c38f6dd209baac

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    أخرىthe vessel was purged with argon
  3. 3
    درجة الحرارةThe reaction was subsequently cooled
  4. 4
    ترشيحfiltered through a bed of celite
  5. 5
    أخرىThe filtrate was evaporated in vacuo
  6. 6
    أخرىSilica gel chromatography (ethyl acetate:hexanes) and evaporation in vacuo of the requisite fractions

الإجراء التجريبي

t-butyl 3-(5-iodo-4-(methylamino)-4aH-pyrrolo[2,3-d]pyrimidin-7(7aH)-yl)propanoate (123 mmol) from above was placed in a 25 ml round bottom flask, whereupon 3.1 ml dimethoxy ethyleneglycol was added. 3-Hydroxyphenylboronic acid (492 mmol pre-dissolved in 0.66 ml ethanol) was added at once, and was followed by 0.5 ml saturated aqueous sodium carbonate. Pd0(PPh3)4 (14 mg, 12 umol) was added to the reaction, the vessel was purged with argon, and set to stir at 80 C overnight. The reaction was subsequently cooled, and filtered through a bed of celite. The filtrate was evaporated in vacuo, and the residual material was adhered to silica gel using ethyl acetate as solvent. Silica gel chromatography (ethyl acetate:hexanes) and evaporation in vacuo of the requisite fractions yielded the desired product. MS m/z=369.22.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07429596B2uspto-grants-2008_09