반응 #1014097

ord-cd0762a8e08e4d948b65eecd9e505251

반응 방정식

CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
CC(C)(C)OC(=O)[C@@H](CCCCN)C(=O)OCC[Si](C)(C)C
(S)-tert-butyl 6-amino-2-((2-(trimethylsilyl)ethoxy)carbonyl)hexanoate
COC(=O)/C=C/C(=O)[O-]
monomethyl fumarate
CCN(C(C)C)C(C)C
DIEA
COC(=O)/C=C/C(=O)NCCCC[C@@H](C(=O)OCC[Si](C)(C)C)C(=O)OC(C)(C)C
(S,E)-tert-butyl 6-(4-methoxy-4-oxobut-2-enamido)-2-((2-(trimethylsilyl)ethoxy)carbonyl)hexanoate
수율 87.8%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The resulting reaction mixture
  2. 2
    농축concentrated under reduced pressure
  3. 3
    workup.ADDITIONThe resulting residue was diluted with EtOAc (50 mL)
  4. 4
    세척washed with brine
  5. 5
    건조dried over Na2SO4
  6. 6
    농축concentrated under reduced pressure
  7. 7
    기타Purification by silica gel chromatography (EtOAc/pentane)

실험 절차

To a stirring mixture of (S)-tert-butyl 6-amino-2-((2-(trimethylsilyl)ethoxy)carbonyl)hexanoate (800 mg, 2.31 mmol), monomethyl fumarate (361 mg, 2.77 mmol), DIEA (1.1 mL, 6.93 mmol) in 10 mL acetonitrile was added HATU (1.14 g, 3.00 mmol) in one portion at 0° C. under an inert atmosphere of argon. The resulting reaction mixture was stirred at room temperature tor 2 h and then concentrated under reduced pressure. The resulting residue was diluted with EtOAc (50 mL) and washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Purification by silica gel chromatography (EtOAc/pentane) afforded (S,E)-tert-butyl 6-(4-methoxy-4-oxobut-2-enamido)-2-((2-(trimethylsilyl)ethoxy)carbonyl)hexanoate (900 mg, 85%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09289503B2uspto-grants-2016_03