Реакция #969865

ord-32af0747c8a44f1dbeed0631b5e4ab5d

Уравнение реакции

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

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08236330B2uspto-grants-2012_08