1,2-Dichloroethane → n-Benzyloxy-3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionamide
Reaction equation
[O:1]=[C:2]1[C:7]([CH2:8][CH2:9][C:10]([OH:12])=O)=[CH:6][CH2:5][CH2:4][NH:3]1.[CH2:13]([O:20][NH2:21])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.Cl.C(N(C(C)C)C)(C)C.C(Cl)CCl>CN(C=O)C.CN(C1C=CN=CC=1)C.C(OCC)(=O)C>[CH2:13]([O:20][NH:21][C:10](=[O:12])[CH2:9][CH2:8][C:7]1[C:2](=[O:1])[NH:3][CH2:4][CH2:5][CH:6]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
29 mg of 3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionic acid (g) was dissolved in 0.5 ml of DMF solution (0.171 mM). 30 mg of BnONH2—HCl (0.188 mM), 0.033 ml of diisopropyl methylamine (0.189 mM), 43 mg of EDC (0.224 mM) and 5 mg of DMAP (0.041 mM) were added thereto and the mixture was stirred for overnight at room temperature. The mixture was diluted with 7 ml of ethyl acetate and washed with 5% HCl (1 ml) and 1 ml of sat. NaHCO3 solution. The organic layer was dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting compound was purified by column chromatography on Silica gel with methanol/chloroform (1:20) solvent mixture as an eluant to give 126 mg of the title compound (h) (yield: 55%).
Workup
- washwashed with 5% HCl (1 ml) and 1 ml of sat. NaHCO3 solution
- dry with materialThe organic layer was dried over anhydrous MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe resulting compound was purified by column chromatography on Silica gel with methanol/chloroform (1:20) solvent mixture as an eluant
Sources & evidence
- ORD record
- ord-5a6ca92aab1f47f393b1c4d96eb65352
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07723376B2
Reaction notes
Loading…