تفاعل #2275700

ord-5feb9f9740f445e798ec61e2866b29a8

معادلة التفاعل

Cl
HCl
COC(=O)CNC(=O)c1ncc(-c2cccc(Cl)c2)cc1O
{[5-(3-chloro-phenyl)-3-hydroxy-pyridine-2-carbonyl]-amino}-acetic acid methyl ester
[Na+].[OH-]
NaOH
O=C(O)CNC(=O)c1ncc(-c2cccc(Cl)c2)cc1O
desired product
المردود 64.0%
O=C(O)CNC(=O)c1ncc(-c2cccc(Cl)c2)cc1O
{[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}-acetic acid
المردود 64.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe solvent removed under reduced pressure
  2. 2
    ترشيحfiltered
  3. 3
    تجفيفthe filtrate dried (MgSO4)
  4. 4
    ترشيحfiltered
  5. 5
    تركيزre-concentrated under reduced pressure
  6. 6
    أخرىThe crude material is triturated with a small amount of MeOH

الإجراء التجريبي

To a solution of {[5-(3-chloro-phenyl)-3-hydroxy-pyridine-2-carbonyl]-amino}-acetic acid methyl ester, 6, (0.163 g, 0.509 mmol) in THF (5 mL) is added 1M NaOH (1.5 ml, 1.27 mmol) and the reaction mixture stirred at room temperature for 1 hour. The solution is acidified using 1M HCl (3 mL), the solvent removed under reduced pressure and the resulting solid suspended in CHCl3:iso-propanol (1:1), filtered and the filtrate dried (MgSO4), filtered and re-concentrated under reduced pressure. The crude material is triturated with a small amount of MeOH to afford 0.10 g (64% yield) of the desired product as a colorless solid. 1H NMR (400 MHz, MeOD) δ ppm 8.31 (1H, d, J=1.8 Hz), 7.47 (2H, d, J=1.8 Hz), 7.30-7.65 (4H, m), 4.07 (2H, s). HPLC-MS: m/z 307 [M+H]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08323671B2uspto-grants-2012_12