반응 #42354

ord-3a6d45f534d84890bb6cdaeead0fbfe5

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction is partitioned between ethyl acetate and water
  2. 2
    세척The organic layer is washed with 1 N hydrochloric acid, saturated sodium bicarbonate, and brine
  3. 3
    건조dried (sodium sulfate)
  4. 4
    여과filtered
  5. 5
    농축concentrated under reduced pressure
  6. 6
    기타Purification by flash column chromatography (silica, 8% methanol/chloroform)

실험 절차

To methyl hydrogen isophthalate (1.0 g, 5.6 mmol) in DMF/chloroform (1:2, 15 mL) is added diisopropylethylamine (3.9 mL, 22 mmol), HATU (2.5 g, 6.7 mmol), then (2R,3S)-3-amino-4-(3,5-difluorophenyl)-1-[(3-ethylbenzyl)amino]butan-2-ol dihydrochloride prepared by the method of Example SP-272 (2.5 g, 6.1 mmol). The reaction is stirred 1 h at room temperature. The reaction is partitioned between ethyl acetate and water. The organic layer is washed with 1 N hydrochloric acid, saturated sodium bicarbonate, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 8% methanol/chloroform) gives the title compound. ESI MS m/z 497.3 [M+H]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07727997B2uspto-grants-2010_06