Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | HCID 18981809 | HCID 18981809 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18005041 | HCID 18005041 | — |
Reaction Steps
A mixture of-3.20 g of 4-amino-5-chloro-2-methoxy-N-(4-piperidinyl)benzamide hydrochloride, 1.22 ml of ethyl bromoacetate, 3.04 g of porassium carbonate, and 32 ml of N,N-dimethylformamide was stirred for 2.5 hours with heating at 60° C. The reaction mixture was concentrated under reduced pressure, and then the residue was added with water and extracted with dichloromethane. The extract was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to give brown oil. The result was converted to the hydrochloride by an ordinary method to afford 3.31 g of pale yellow crystals. Recrystallization from ethanol gave colorless plates, m.p. 196.5°-198.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05500422 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-aa72f40674a44859be63be9477007b86 |
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| Source note | uspto-grants-1996_03 |
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