HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608201Generated: October 30, 2026
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → 4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2-hydroxybenzamide
https://huagongshe.com/reaction/1608201
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (4-Benzylmorpholin-2-yl)methanamine | HCID 2776360 | — |
| Reactant | 2-Acetoxy 4-acetamino 5-chlorobenzoic acid | HCID 19848610 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2-hydroxybenzamide | HCID 14881978 | 54.2% |
Reaction Steps
To a mixture of 2-aminomethyl-4-benzylmorpholine (3.1 g), 2-acetoxy-4-acetylamino-5-chlorobenzoic acid (4.0 g), and dichloromethane (40 ml) is added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (2.9 g), and the mixture is stirred at 25° C. for 4 hours. The reaction mixture is washed successively with water and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and evaporated under reduced pressure. The residue is dissolved in ethanol (80 ml), and 10% hydrochloric acid (30 ml) is added. The mixture is refluxed with stirring for 2 hours and concentrated under reduced pressure. The residue is neutralized with aqueous sodium bicarbonate solution and extracted with chloroform. The organic layer is washed successively with water and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and evaporated under reduced pressure. The residue is recrystallized from isopropyl alcohol to give the monohydrate of the title compound (3.0 g), mp 153°-155° 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-eb9b7fad51c3452fae30ef1de43531c4 |
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| Source note | uspto-grants-1989_09 |
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