Реакция #1929059

ord-dd9e8be36a084d9cbe28ba917b2ccb68

Уравнение реакции

C#CCOc1ccc(C[C@H](N)C(=O)O)cc1
p-propargyloxyphenylalanine
Cl
HCl
NC(Cc1ccccc1)C(=O)O
2-Amino-3-phenylpropionic acid
O
Water
C#CCOC(=O)C(N)Cc1ccc(OCC#C)cc1
2-Amino-3-[4-(prop-2-ynyloxy)phenyl]-propionic acid propargyl ester

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITthe mixture was kept at 4° C. overnight
  2. 2
    ФильтрацияThe precipitate was filtered
  3. 3
    Промывкаwashed with ice-cold H2O
  4. 4
    Другоеdried under vacuum
  5. 5
    Другоеyielding

Методика

The propargyl ester (1.6 g, 5.5 mmol) from the previous step was dissolved in a mixture of aqueous 2 N NaOH (14 mL) and MeOH (10 mL). After stirring for 1.5 h at room temperature, the pH was adjusted to 7 by adding conc. HCl. Water (20 mL) was added and the mixture was kept at 4° C. overnight. The precipitate was filtered, washed with ice-cold H2O, and dried under vacuum yielding, 1.23 g (90%) of 11n FIG. 11 (2-Amino-3-phenylpropionic acid (1) (also known as p-propargyloxyphenylalanine) as a white solid, 1H NMR (400 MHz, D2O) (as the potassium salt in D2O) δ 7.20 (d, J=8.8 Hz, 2H), 6.99 (d, J=8.8 Hz, 2H), 4.75 (s, 2H), 3.50 (dd, J=5.6, 7.2 Hz, 1H), 2.95 (dd, J=5.6, 13.6 Hz, 1H), 2.82 (dd, J=7.2, 13.6 Hz, 1H); 13C NMR (100 MHz, D2O) δ 181.3, 164.9, 155.6, 131.4, 130.7, 115.3, 57.3, 56.1, 39.3; HRMS (CI) m/z 220.0969 [C12H13NO3 (M+1) requires 220.0968].

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08945926B2uspto-grants-2015_02