반응 #8752

ord-35056de0b49747e79ad154c41ebc6c38

반응 방정식

BrCCCOc1cccc(-c2noc3ccsc23)c1
3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole
ClCCCOc1cccc(-c2noc3ccsc23)c1
3-[3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole
NCCc1ccc(S(N)(=O)=O)cc1
4-(2-aminoethyl) benzenesulfonamide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
NS(=O)(=O)c1ccc(CCNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
title compound
수율 35.0%
NS(=O)(=O)c1ccc(CCNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
4-{2-[3-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-propylamino]-ethyl}-benzenesulfonamide
수율 35.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척is eluted
  2. 2
    workup.ADDITIONa graded solvent mixture of dichloromethane:methanol (90:10)
  3. 3
    농축Combine the appropriate fractions and concentrate

실험 절차

The title compound is prepared from a mixture of 3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 3-[3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 4-(2-aminoethyl) benzenesulfonamide and potassium carbonate essentially as described above in example 4 except that the column is eluted using a graded solvent mixture of dichloromethane:methanol (90:10). Combine the appropriate fractions and concentrate to give the title compound (0.16 g, 35% Yield) as a solid. Purity by LC/MS (APCI)=96% area, [M+H]+=458 m/e.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091199B1uspto-grants-2006_08