Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2H-1-Benzopyran-2-one, 3-acetyl-7-(diethylamino)- | HCID 688763 | — |
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | HCID 19438375 | HCID 19438375 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53828296 | HCID 53828296 | — |
Reaction Steps
3-acetyl-7-diethylaminocoumarin (1.04 g, prepared according to the procedure described in U.S. Pat. No. 4,147,552), 1.20 g N-(2-piperidinoethyl)-N-ethyl-4-aminobenzaldehyde, 0.10 g piperidinium acetate, and 40 ml toluene were placed in a 100 ml round-bottomed flask fitted with a Dean-Stark trap and condenser. The solution was refluxed for 16 hr with removal of collected water. The toluene was evaporated under reduced pressure and a mixture of 20 ml water and 5 ml ethanol was added to the resultant viscous material. Upon stirring a solid precipitated which was isolated by filtration and drying to give 1.5 g of 7-diethylamino-3-(3-(N-ethyl-N-(2-piperidinoethyl)-4-aminophenyl)propenoyl)coumarin (4) as a red solid; λmax (ethanol)=475 nm. ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05480994 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-f5f0db41c7d64cb8bef7b21e4dea0fc2 |
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| Source note | uspto-grants-1996_01 |
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