4-Amino-5-chloro-2-methoxybenzoic acid → 4-amino-5-chloro-N-[(4-ethoxycarbonyl-2-morpholinyl)methyl]-2-methoxybenzamide
Reaction equation
[NH2:1][CH2:2][CH:3]1[O:8][CH2:7][CH2:6][N:5]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:4]1.[NH2:14][C:15]1[C:23]([Cl:24])=[CH:22][C:18]([C:19](O)=[O:20])=[C:17]([O:25][CH3:26])[CH:16]=1.Cl.C(N=C=NCCCN(C)C)C>ClCCl>[NH2:14][C:15]1[C:23]([Cl:24])=[CH:22][C:18]([C:19]([NH:1][CH2:2][CH:3]2[O:8][CH2:7][CH2:6][N:5]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:4]2)=[O:20])=[C:17]([O:25][CH3:26])[CH:16]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
To a solution of 2-aminomethyl-4-ethoxycarbonylmorpholine (5.8 g) in dichloromethane (100 ml), 4-amino-5-chloro-2-methoxybenzoic acid (5.0 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (5.2 g) are added, and the resulting mixture is stirred at 25° C. for 4 hours. The reaction mixture is washed successively with water, aqueous sodium hydroxide solution and saturated aqueous sodium chloride solution, and dried over magnesium sulfate. The solvent is distilled off under reduced pressure. The residue is dissolved in chloroform and chromatographed on silica gel. The eluate with chloroform is discarded, and the subsequent eluates with methanol-chloroform (1:9) are pooled and evaporated to give the title compound (7.5 g) as an oil.
Workup
- washThe reaction mixture is washed successively with water, aqueous sodium hydroxide solution and saturated aqueous sodium chloride solution
- dry with materialdried over magnesium sulfate
- distillationThe solvent is distilled off under reduced pressure
- dissolutionThe residue is dissolved in chloroform
- customchromatographed on silica gel
- customevaporated
Sources & evidence
- ORD record
- ord-50147ce3283a4e3f91f06ffb648bcc5a
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04870074
Reaction notes
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