반응 #607430

ord-f2691f54a909430594c34430c2b00933

반응 방정식

Cn1oc(=O)nc1/C(=N\OCc1csc(N)n1)c1ccccc1
3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-methyl-1,2,4-oxadiazol-5(2H)-one
c1ccncc1
pyridine
O=C(Cl)C1COc2ccccc2O1
2,3-dihydro-1,4-benzodioxine-2-carbonyl chloride
Cn1oc(=O)nc1/C(=N\OCc1csc(NC(=O)C2COc3ccccc3O2)n1)c1ccccc1
N-{4-[({[(Z)-(2-methyl-5-oxo-2,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methylene]amino}oxy)methyl]-1,3-thiazol-2-yl}-2,3-dihydro-1,4-benzodioxine-2-carboxamide
수율 106.4%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction was quenched by addition of water
  2. 2
    농축concentrated to dryness
  3. 3
    workup.ADDITION0.5 ml of 1N NaOH was added
  4. 4
    여과The solution was filtered through a chemelut pad
  5. 5
    세척washed with EtOAc
  6. 6
    농축After concentration
  7. 7
    기타the residue was purified by chromatography on silica gel

실험 절차

To a solution of 3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-methyl-1,2,4-oxadiazol-5(2H)-one (120 mg, 0.362 mmol, 1 eq.) and pyridine (0.044 ml, 0.543 mmol, 1.5 eq) in dry dichloromethane (2.0 ml) at room temperature was added 2,3-dihydro-1,4-benzodioxine-2-carbonyl chloride (108 mg, 0.543 mmol, 1.5 eq) and stirring was allowed overnight. The reaction was quenched by addition of water and concentrated to dryness. The residue was taken in EtOAc and 0.5 ml of 1N NaOH was added. The solution was filtered through a chemelut pad and washed with EtOAc. After concentration, the residue was purified by chromatography on silica gel to give N-{4-[({[(Z)-(2-methyl-5-oxo-2,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methylene]amino}oxy)methyl]-1,3-thiazol-2-yl}-2,3-dihydro-1,4-benzodioxine-2-carboxamide (190 mg, 99% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09326515B2uspto-grants-2016_05