반응 #607434

ord-e0eee15586c04438aab6348bacf0f8ff

반응 방정식

OC1CCCCC1
Cyclohexanol
c1ccncc1
pyridine
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
CC#N
acetonitrile
COc1cccc(/C(=N/OCc2csc(NC(=O)OC3CCCCC3)n2)c2nc(=O)on2C)c1
Cyclohexyl {4-[({[(Z)-(3-methoxyphenyl)(2-methyl-5-oxo-2,5-dihydro-1,2,4-oxadiazol-3-yl)methylene]amino}oxy)methyl]-1,3-thiazol-2-yl}carbamate
수율 77.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the resulting mixture was refluxed for 15 h
  2. 2
    농축After concentration
  3. 3
    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 (100 mg, 0.277 mmol, 1 eq.) in acetonitrile (2 ml) was added 4-fluorophenylcarbonochloridate (0.040 mL, 0.304 mmol, 1.1 eq.), followed by pyridine (0.022 mL, 0.277 mmol, 1 eq.) and stirring was allowed for 2 hours at room temperature. Cyclohexanol (0.032 mL, 0.304 mmol, 1.1 eq.) was then added and the resulting mixture was refluxed for 15 h. After concentration, the residue was purified by chromatography on silica gel to give Cyclohexyl {4-[({[(Z)-(3-methoxyphenyl)(2-methyl-5-oxo-2,5-dihydro-1,2,4-oxadiazol-3-yl)methylene]amino}oxy)methyl]-1,3-thiazol-2-yl}carbamate (110 mg, 77% yield) as a white solid.

출처

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