反応 #969865

ord-32af0747c8a44f1dbeed0631b5e4ab5d

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe reaction was stirred at room temperature for 12 h
  2. 2
    洗浄washed twice with H2O
  3. 3
    乾燥dried over MgSO4 (anh.)
  4. 4
    その他purified by column chromatography (Hexane:AcOEt 3:1→2:1→AcOEt)

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08236330B2uspto-grants-2012_08