반응 #8278

ord-c6b7e39aa88a417b83bfa4edaf24c448

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도by heating at 45° for 4 hour

실험 절차

Essentially the technique for the appropriate intermediate of Example 22 was used, but substituting 3-(t-butoxycarbonylamino)pyridazine (293 mg, 1.5 mM) for the pyrazine analogue. The reaction was carried out by heating at 45° for 4 hour, and the chromatography was carried out with a gradient from 0% to 100% ethyl acetate in dichloromethane. Relevant fractions were combined to give the desired product (315 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087629B2uspto-grants-2006_08