반응 #1105330

ord-43e9ffc88bb44e7aa3d3d7196f730c4a

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척then was washed in turn with 0.5N hydrochloric acid (2×250 mL), saturated sodium bicarbonate solution (2×250 mL) and brine (300 mL)
  2. 2
    건조The dried (MgSO4) organic layer
  3. 3
    여과was filtered
  4. 4
    기타evaporated to dryness under reduced pressure
  5. 5
    기타The crude product which was purified by silica gel column chromatography

실험 절차

To a suspension of 4-nitro-L-phenylalanine methyl ester hydrochloride salt (181.84 mmol, 47.41 g), 1-[4-(methylthio)butyl]cyclopentanecarboxylic acid (177.17 mmol, 38.33 g) in DMF (470 mL) were added HBTU (177.17 mmol, 67.2 g) and diisopropylethylamine (443 mmol, 77 mL) at room temperature. The clear solution was stirred for 15 h at room temperature at which time TLC analysis of the mixture indicated the absence of starting materials. The reaction mixture was diluted with 600 mL of ethyl acetate then was washed in turn with 0.5N hydrochloric acid (2×250 mL), saturated sodium bicarbonate solution (2×250 mL) and brine (300 mL). The dried (MgSO4) organic layer was filtered and evaporated to dryness under reduced pressure. The crude product which was purified by silica gel column chromatography to afford 58.5 g (78%) of N-[[1-[4-(methylthio)butyl]cyclopentyl]carbonyl]-4-nitro-L-phenylalanine methyl ester as an amorphous colorless solid. HRMS: Obs. mass, 423.1940. Calcd. mass, 423.1953 (M+H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06479666B2uspto-grants-2002_11