HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 19898753, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Oxalate | HCID 71081 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | ethyl 7-hydroxy-4-oxo-4H-chromen-2-carboxylate | HCID 5376802 | — |
| Reactant | HCID 19898752 | HCID 19898752 | — |
| Reactant | HCID 19898770 | HCID 19898770 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19898753 | HCID 19898753 | 69% |
Reaction Steps
The same procedure as in Example 8-(2) was effected so as to react and treat 0.6 g of N-ethyl-N-(2-hydroxyethyl)-N'[1,3-dimethyl-2,4-dioxopyrimidine-6-yl]ethylenediamine (Compound 32), 0.57 g of 2-ethoxycarbonyl-7-hydroxy-4-oxo-4H-1-benzopyran (Compound 33), 30 ml of tetrahydrofuran containing 0.77 g of triphenylphosphine and 0.47 ml of diethyl azodicarboxylate, thereby obtaining 0.81 g (yield 69%) of oily 1,3-dimethyl-6-(2-[N-ethyl-N-[2-(2-ethoxycarbonyl-4-oxo-4H-1-benzopyran-7-yl)oxyethyl]amino]ethylamino)-2,4(1H,3H)-pyrimidinedione (the non-oxalate of Compound 34).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05114941 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-835f228946be43fe8ef7303be9daec2e |
| Source note | uspto-grants-1992_05 |