تفاعل #61546

ord-2a22e945624f48da92ba941547177e5e

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was concentrated under reduced pressure
  2. 2
    أخرىthe residue was purified by preparative HPLC (
  3. 3
    غسيلC18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA)
  4. 4
    workup.ADDITIONThe fractions containing the product
  5. 5
    أخرىwere evaporated
  6. 6
    أخرىto yield a white solid

الإجراء التجريبي

To 400 mg 1-[(5-Chloro-pyridin-2-ylcarbamoyl)-methyl]-5-[2-(2-methoxy-ethoxy)-ethoxymethyl]-1H-pyrazole-3-carboxylic acid in 5 ml DCM and 0.3 ml NEt3, 217 mg 1-Isopropyl-piperidin-4-ylamine hydrochloride and 250 mg BOP-Cl were added at RT and the rmixture was stirred for 16 h. The mixture was concentrated under reduced pressure and the residue was purified by preparative HPLC (C18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA). The fractions containing the product were evaporated and lyophilized to yield a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07429581B2uspto-grants-2008_09