반응 #6207

ord-2c8dc63242cc44cab385e6bb518c6cff

반응 방정식

NCCCSc1ccncc1
4-(3-aminopropylthio)pyridine
CC(C)(C)c1cc(C(=O)O)cc(C(C)(C)C)c1O
3,5-di-t-butyl-4-hydroxybenzoic acid
O=C1CCC(=O)N1O
N-hydroxysuccinimide
CCN=C=NCCCN(C)C.Cl
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride
CC(C)(C)c1cc(C(=O)NCCCSc2ccncc2)cc(C(C)(C)C)c1O
desired compound
수율 27.3%
CC(C)(C)c1cc(C(=O)NCCCSc2ccncc2)cc(C(C)(C)C)c1O
4-[3-(3,5-di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridine
수율 27.3%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooling
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 30 minutes
  3. 3
    workup.STIRRINGthe mixture was stirred at rcom temperature for 8 hours
  4. 4
    세척The reaction mixture was washed with water
  5. 5
    기타dried
  6. 6
    workup.DISTILLATIONThe solvent was distilled off
  7. 7
    기타The residue was purified by column chromatography (eluent: ethyl acetate)

실험 절차

To a solution of 1.49 g (5.94 mmol) of 3,5-di-t-butyl-4-hydroxybenzoic acid and 889 mg (7.73 mmol) of N-hydroxysuccinimide in 60 ml of methylene chloride was added 1.38 g (7.13 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. Further 1.00 g (5.94 mmol) of 4-(3-aminopropylthio)pyridine was added and the mixture was stirred at rcom temperature for 8 hours. The reaction mixture was washed with water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 650 mg of the desired compound (27.3%, colorless powder), mp: 203.0°-204.0° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05246948uspto-grants-1993_09