Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl chloromalonate | HCID 86762096 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
Reaction Steps
About 200 mg of (4) are swollen in solvent in the cold (e.g. at 0° C. in DMF) and treated with about 1 mmol of monomethyl chloromalonate. About 0.5 ml of triethylamine is added and the mixture is stirred for about 2 h at 0° C. and for 1 h at a low heat (e.g. 50° C.). After washing the resin (3) is isolated. The free derivative of the N,N′-dialkylbarbituric acid (3, Li-P=H) is then obtained by removal of the linker.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399653B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-a2f9dfa15e6b4eb28d4259802a6230a4 |
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| Source note | uspto-grants-2002_06 |
|---|