HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 11587404, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzoyl isocyanate | HCID 78210 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 9971786 | HCID 9971786 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11587404 | HCID 11587404 | 85.2% |
Reaction Steps
1.0 g (6.8 mmol) benzoylisocyanate is added to 1.0 g (3.4 mmol) 3-amino-4-methyl-6-phenyl-furo[2,3-b]pyridine-2-carboxylic acid ethyl ester (described in Wagner G., Prantz J. Pharmazie 1990, 45, 213-214) in 20 ml absolute acetone and stirred at room temperature for 30 minutes. The solvent is removed and the precipitate precipitated after the addition of water is sucked off and dried. The resulting precipitate is refluxed with 0.46 g (6.8 mmol) NaOEt and 20 ml ethanol for 15 min. Then, 20 ml water is added, the precipitate is sucked off, washed with some ethanol and dried. 0.85 g (85%) 9-methyl-7-phenyl-pyrido[3′,2′:4,5]furo[3,2-d]pyrimidin-2,4-dione is obtained
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058285B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-418873c7e0ca4778a6200c8c284dfb89 |
| Source note | uspto-grants-2011_11 |