반응 #6259

ord-d55965f78437450f9aef72b94ae9f168

반응 방정식

Cl.Cl.NCCCSc1ccncc1
4-(3-aminopropylthio)pyridine dihydrochloride
O=C(O)c1cnccn1
2-pyrazinecarboxylic acid
O=C1CCC(=O)N1O
N-hydroxysuccinimide
CCN=C=NCCCN(C)C.Cl
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride
O=C(NCCCSc1ccncc1)c1cnccn1
desired compound
수율 34.0%
O=C(NCCCSc1ccncc1)c1cnccn1
4-[3-(2-pyrazinecarbonylamino)propylthio]pyridine
수율 34.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooling
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 1 hour
  3. 3
    workup.STIRRINGthe mixture was stirred at room temperature for 3 hours
  4. 4
    세척The reaction mixture was washed with saturated aqueous sodium bicarbonate and 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 1.00 g (8.06 mmol) of 2-pyrazinecarboxylic acid and 1.21 g (10.5 mmol) of N-hydroxysuccinimide in 70 ml of methylene-chloride, 1.85 g (9.67 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC) was added with stirring under ice-cooling, and the mixture was stirred at room temperature for 1 hour. Further, 1.94 g (8.06 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride was added, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was washed with saturated aqueous sodium bicarbonate and water, and dried. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate) to give 0.751 g of the desired compound (34.0% yield, colorless powder).

출처

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