반응 #1267677

ord-d0f47cb2c9114d63904c6a3af04d5fcd

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축concentrated in vacuo
  2. 2
    온도The residue was cooled in an ice water bath
  3. 3
    workup.ADDITIONaqueous 3.6 N hydrochloric acid was added
  4. 4
    기타the precipitate collected
  5. 5
    세척rinsed with aqueous 3.6 N hydrochloric acid
  6. 6
    건조water and dried
  7. 7
    기타Recrystallization from ethyl alcohol

실험 절차

A mixture of 4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (179 mg, 1 mmol), aniline (0.46 mL, 5^ mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (959 mg, 5 mmol) in 50% aqueous dioxane (10 mL) was allowed to stir at ambient temperature for 17.5 hours, then concentrated in vacuo. The residue was cooled in an ice water bath, aqueous 3.6 N hydrochloric acid was added, and the precipitate collected, rinsed with aqueous 3.6 N hydrochloric acid then water and dried. Recrystallization from ethyl alcohol afforded N-phenyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide (Compound 35) (164 mg). mp 225-226° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07282498B2uspto-grants-2007_10