Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 12769849 | HCID 12769849 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12853016 | HCID 12853016 | 7.7% |
Reaction Steps
1-methylpiperazine (4.5g.) was added dropwise to a suspension of 5-(2-ethoxyethoxy)chromone-2-carboxylic acid (5.0g.) in chloroform (50ml.). A solution of phosphorus tribromide (2.0g.) in chloroform (10ml.) was added dropwise to the resultant mixture under ice cooling for 10 minutes. The mixture was stirred under ice cooling for 2 hours and at room temperature for additional 1 hour, and then ethyl acetate (250ml.) was added to the reaction mixture. The mixture was washed twice with 5% aqueous solution of sodium bicarbonate and with water in turn, and dried. The solvent was distilled off under reduced pressure to give 2-(4-methyl-1-piperazinyl)carbonyl-5-(2-ethoxyethoxy) chromone (500mg.). The product was derived in the usual manner to its maleate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001280 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-89b0ce1fe15e437b89c43a3c2514312c |
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| Source note | uspto-grants-1977_01 |
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