Реакция #2275712

ord-c789275dfc054a4c9cc74f560154b448

Уравнение реакции

Cl
HCl
COC(=O)CNC(=O)c1cc(-c2ccc(C)cc2)ccn1
[(4-(4-methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid methyl ester
O
H2O
O.[Li][OH]
LiOH.H2O
Cc1ccc(-c2ccnc(C(=O)NCC(=O)O)c2)cc1
desired compound
Выход 12.0%
Cc1ccc(-c2ccnc(C(=O)NCC(=O)O)c2)cc1
[(4-(4-Methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid
Выход 12.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvents are removed under reduced pressure
  2. 2
    workup.ADDITIONthe solid that remains is suspended in a mixture of THF
  3. 3
    ФильтрацияMeOH and filtered
  4. 4
    КонцентрированиеThe filtrate is concentrated under reduced pressure
  5. 5
    Другоеthe resulting solid is triturated with MeOH
  6. 6
    Фильтрацияcollected by filtration

Методика

To a solution of [(4-(4-methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid methyl ester, 24, (0.092 g, 0.32 mmol) in THF (2 mL) at room temperature is added H2O (1 mL) and LiOH.H2O (0.027 g, 0.64 mmol). The reaction is stirred for 16 hours after which time the solution is acidified using 1M HCl. The solvents are removed under reduced pressure and the solid that remains is suspended in a mixture of THF: MeOH and filtered. The filtrate is concentrated under reduced pressure and the resulting solid is triturated with MeOH and collected by filtration to provide 0.012 g (12% yield) of the desired compound as a colorless solid. 1H NMR (250 MHz, MeOD) δ ppm 8.69 (1H, d, J=4.8 Hz), 8.38 (1H, s), 7.86 (1H, d, J=6.2 Hz), 7.72 (2H, d, J=8.1 Hz), 7.38 (1H, d, J=7.9 Hz), 4.21 (1H, s), 2.44 (2H, s). HPLC-MS: m/z 271 [M+H]+.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08323671B2uspto-grants-2012_12