Реакция #61062

ord-d66272e0d7394d17aa10de1cb71524d7

Уравнение реакции

O=CC(=O)c1ccccc1
phenyl glyoxal
CC(C)(C)OC(=O)NCCc1ccc(N)cc1
4-(N-Boc-2-aminoethyl)aniline
[BH3-]C#N.[Na+]
NaCNBH3
CC(C)(C)OC(=O)NCCc1ccc(NCC(O)c2ccccc2)cc1
N-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)-aniline
Выход 91.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеconcentrated
  2. 2
    Другоеpurified by flash silica column chromatography (2 to 5% MeOH/CH2Cl2)

Методика

4-(N-Boc-2-aminoethyl)aniline 28 (1.25 g, 5.29 mmole) was dissolved in methanol (30 mL), followed by addition of phenyl glyoxal 24 (0.708 g, 5.28 mmole). The reaction mixture was stirred for 1 h at rt, prior to addition of NaCNBH3 (0.665 g, 10.6 mmole). The final mixture was stirred for 12 h at rt, concentrated, and purified by flash silica column chromatography (2 to 5% MeOH/CH2Cl2) to give N-(2-phenyl-2-hydroxyethyl)-4-(N-Boc-2-aminoethyl)-aniline as a pale yellow oil (1.71 g, 91%): Rf=0.18 in 5% MeOH/CH2Cl2. 1H-NMR (CD3OD, 299.96 MHz): δ (ppm) 7.47.25 (m, 5H), 7.0-6.95 (d, 2H), 6.63-6.60 (d, 2H), 4.85-4.79 (dd, 1H), 3.3-3.21 (t, 2H), 3.2-3.15 (m, 2H), 2.64-2.5 (t, 2H), 1.42 (s, 9H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07427639B2uspto-grants-2008_09