تفاعل #2275712

ord-c789275dfc054a4c9cc74f560154b448

معادلة التفاعل

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
المردود 12.0%
Cc1ccc(-c2ccnc(C(=O)NCC(=O)O)c2)cc1
[(4-(4-Methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid
المردود 12.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvents are removed under reduced pressure
  2. 2
    workup.ADDITIONthe solid that remains is suspended in a mixture of THF
  3. 3
    ترشيحMeOH and filtered
  4. 4
    تركيزThe filtrate is concentrated under reduced pressure
  5. 5
    أخرىthe resulting solid is triturated with MeOH
  6. 6
    ترشيحcollected by filtration

الإجراء التجريبي

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]+.

المصدر

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