Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalate | HCID 71081 | — |
| Reactant | 1,3-Dimethyl-6-(piperazin-1-yl)pyrimidine-2,4(1H,3H)-dione | HCID 12816873 | — |
| Reactant | HCID 19898732 | HCID 19898732 | — |
| Reactant | HCID 19898792 | HCID 19898792 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 19898733 | HCID 19898733 | 84% |
Reaction Steps
To 2 ml of N,N-dimethylformamide were added 0.78 g of the previously obtained 3-(2,3-dimethyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl bromide (Compound 6), 0.9 g of 1,3-dimethyl-6-(piperazine-1-yl)-2,4(1H,3H)-pyrimidinedione (Compound 3) and 3 ml of triethylamine, and the solution was then heated at 100° C. for 3 hours in order to carry out reaction. The resultant reaction solution was treated and then purified in the same manner as in Example 1-(2) to obtain 0.96 g (yield 84%) of 1,3-dimethyl-6-(4-[3-(2,3-dimethyl-4-oxo-4H-1-benzopyran-5-yl)oxypropyl]piperazine-1-yl)-2,4(1H,3H)-pyrimidinedione (the non-oxalate of Compound 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05114941 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-363f3e01ee04469ea5d77a4113ccf7fd |
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| Source note | uspto-grants-1992_05 |
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