Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-Aminomethyl-4-(4-fluorobenzyl)morpholine | HCID 10242735 | — |
| Reactant | 4-Amino-5-chloro-2-ethoxybenzoic acid | HCID 10536658 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Mosapride | HCID 119584 | 72.7% |
Reaction Steps
To a stirred suspension of 4-amino-5-chloro-2-ethoxybenzoic acid (2.9 g) in dichloromethane (50 ml), triethylamine (1.6 g) is added at 25° C. The resulting mixture is cooled to -10° C., and isobutyl chloroformate (2.0 g) is added slowly. After the mixture is stirred at the same temperature for 1 hour, a solution of 2-aminomethyl-4-(4-fluorobenzyl)morpholine (3.0 g) in dichloromethane (10 ml) is added. The reaction mixture is stirred for 1 hour at a temperature of between -10° C. and -5° C. and then at 25° C. overnight. The mixture is washed successively with water, 10% aqueous sodium hydroxide solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and evaporated under reduced pressure. The residue is recyrstallized from ethanol to give the title compound (4.1 g), mp 151°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04870074 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-138022e7f82d469686cb14aadee064ee |
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| Source note | uspto-grants-1989_09 |
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