Réaction #2275696

ord-267c8bb64fe54009a84b95ec665bc546

Équation de réaction

Cl.O=C(O)c1ncc(OCc2ccccc2)cc1OCc1ccccc1
3,5-bis-benzyloxy-pyridine-2-carboxylic acid HCl
CCN(C(C)C)C(C)C
diisopropylethylamine
CCN=C=NCCCN(C)C
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
On1nnc2ccccc21
1-hydroxybenzotriazole
COC(=O)CN.Cl
glycine methyl ester hydrochloride
COC(=O)CNC(=O)c1ncc(OCc2ccccc2)cc1OCc1ccccc1
desired product
Rendement 40.0%
COC(=O)CNC(=O)c1ncc(OCc2ccccc2)cc1OCc1ccccc1
[(3,5-bis-benzyloxy-pyridine-2-carbonyl)-amino]-acetic acid methyl ester
Rendement 40.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGstirred 3 days
  2. 2
    ConcentrationThe reaction volume is partially concentrated under reduced pressure
  3. 3
    workup.ADDITIONthen diluted with EtOAc
  4. 4
    Lavagewashed with saturated aqueous NaHCO3 and saturated aqueous NaCl
  5. 5
    SéchageThe organic layer is dried (MgSO4)
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated under reduced pressure
  8. 8
    Autreto afford a yellow oil that
  9. 9
    Autreis purified over silica (EtOAc:heptane gradient 1:1 to 1:0)

Mode opératoire

To a solution of 3,5-bis-benzyloxy-pyridine-2-carboxylic acid HCl, 2, (8.06 g, 21.7 mmol) in DMF (100 mL) at 0° C. under N2 is added diisopropylethylamine (11.35 mL, 65.1 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDCI) (6.23 g, 32.6 mmol) and 1-hydroxybenzotriazole (HOBt) (0.294 g, 2.2 mmol). The solution is stirred for 5 minutes and glycine methyl ester hydrochloride (4.09 g, 32.6 mmol) is added. The reaction is allowed to warm slowly to room temperature and stirred 3 days. The reaction volume is partially concentrated under reduced pressure then diluted with EtOAc and washed with saturated aqueous NaHCO3 and saturated aqueous NaCl. The organic layer is dried (MgSO4), filtered and concentrated under reduced pressure to afford a yellow oil that is purified over silica (EtOAc:heptane gradient 1:1 to 1:0) to afford 3.5 g (40% yield) of the desired product as a yellow oil. 1H NMR (400 MHz, CDCl3) δ ppm 8.12 (1H, t, J=4.9 Hz), 7.95 (1H, d, J=1.8 Hz), 7.38-7.44 (2H, m), 7.22-7.35 (8H, m), 6.85 (1H, d, J=2.6 Hz), 5.14 (2H, s), 5.03 (2H, s), 4.18 (2H, d, J=5.5 Hz), 3.69 (3H, s). HPLC-MS: m/z 407 [M+H]+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08323671B2uspto-grants-2012_12