반응 #61546

ord-2a22e945624f48da92ba941547177e5e

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The mixture was concentrated under reduced pressure
  2. 2
    기타the residue was purified by preparative HPLC (
  3. 3
    세척C18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA)
  4. 4
    workup.ADDITIONThe fractions containing the product
  5. 5
    기타were evaporated
  6. 6
    기타to yield a white solid

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07429581B2uspto-grants-2008_09