반응 #1269814

ord-2ca7a0b4be9d42a18bbf1117af8d3121

반응 방정식

NCCCC[C@H](N)C(=O)O
Lysine
C=CCOC(=O)CC[C@H](N)C(=O)OCC=C
diallyl glutamate
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
CCN(CC)CC
Et3N
O=C1c2ccccc2C(=O)C1(O)O
ninhydrin

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe reaction was stirred at room temperature for 12 h
  2. 2
    세척washed twice with H2O
  3. 3
    건조dried over MgSO4 (anh.)
  4. 4
    기타purified by column chromatography (Hexane:AcOEt 3:1→2:1→AcOEt)

실험 절차

To a stirred solution of diallyl glutamate (3.96 g, 15 mmol) and triphosgene (1.47 g, 4.95 mmol) in CH2Cl2 (143 mL) at −78° C. was added Et3N (6.4 mL, 46 mmol) in CH2Cl2 (28 mL). The reaction mixture was allowed to warm to room temperature and stirred for 1.5 h. The Lysine derivative (2.6 g, 9.09 mmol) in a solution of CH2Cl2 (36 mL) was then added at −78° C. and the reaction was stirred at room temperature for 12 h. The solution was diluted with CH2Cl2, washed twice with H2O, dried over MgSO4 (anh.) and purified by column chromatography (Hexane:AcOEt 3:1→2:1→AcOEt) to give 4 g (82%) (TLC in CH2Cl2:MeOH 20:1 Rf=0.3, revealed with ninhydrin). 1H-NMR (CDCl3, 300 MHz) δ 5.97-5.84 (m, 3H, 3-CH2CHCH2), 5.50 (bt, 2H, 2NHurea), 5.36-5.20 (m, 6H, 3-CH2CHCH2), 4.81 (bs, 1H, NHBoc), 4.68-4.40 (m, 8H, 3-CH2CHCH2, CH(Lys), CH(glu)), 3.09-3.05 (m, 2H, CH2NHBoc), 2.52-2.39 (m, 2H, CH2(glu.)), 2.25-2.14 and 2.02-1.92 (2m, 2H, CH2(glu.)), 1.87-1.64 (m, 4H, 2CH2(Lys)), 1.51-1.35 (m, 2H, CH2(Lys)), 1.44 (s, 9H, Boc).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08663700B2uspto-grants-2014_03