반응 #2275720

ord-49088874da784ab89d826d849b46d841

반응 방정식

CCOC(=O)CNCC(=O)c1ncccc1O
[(3-hydroxy-pyridine-2-carbonyl)methylamino]acetic acid ethyl ester
O
H2O
[Na+].[OH-]
NaOH
CN(CC(=O)O)C(=O)c1ncccc1O
desired compound
수율 85.0%
CN(CC(=O)O)C(=O)c1ncccc1O
[(3-hydroxy-pyridine-2-carbonyl)-methyl-amino]-acetic acid
수율 85.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축then concentrated under reduced pressure
  2. 2
    농축the solution is concentrated under reduced pressure
  3. 3
    기타to give an off-white solid
  4. 4
    여과then collected by filtration
  5. 5
    세척The solid is washed with additional CHCl3:isopropanol (1:1)
  6. 6
    기타then transferred to a flask
  7. 7
    기타triturated with Et2O

실험 절차

To a solution of [(3-hydroxy-pyridine-2-carbonyl)methylamino]acetic acid ethyl ester, 32, (0.10 g, 0.42 mmol) in THF (4 mL) is added H2O (1 mL) and NaOH (0.90 g, 2.25 mmol). The reaction is stirred for 3 hours then concentrated under reduced pressure. The remaining oil is acidified to pH ˜1 with 1M HCl and the solution is concentrated under reduced pressure to give an off-white solid. The solid is suspended in CHCl3:isopropanol (1:1) then collected by filtration. The solid is washed with additional CHCl3:isopropanol (1:1) then transferred to a flask and triturated with Et2O to afford 0.075 g (85% yield) of the desired compound as a pale yellow solid. 1H NMR (250 MHz, MeOD) δ ppm (rotamers) 8.26 (1H, br s), 7.63-7.74 (1H, m), 7.56-7.63 (1H, m), 4.38 (1H, s), 4.32 (1H, s), 3.20 (1.5H, s), 3.12 (1.5H, s). HPLC-MS: m/z 211 [M+H]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08323671B2uspto-grants-2012_12