HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 22106143, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HCID 22106381 | HCID 22106381 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22106143 | HCID 22106143 | — |
Reaction Steps
To a solution of N-[1-butyl-4-{3-(2-propynyloxy)phenyl}-1,2-dihydro-2-oxo-1,8-naphthyridin-3-yl]-N'-(2,6-diisopropylphenyl)urea (1.0 g, 1.82 mmol) in dioxane (10 ml) were added paraformaldehyde (0.37 g), diethylamine (0.26 g, 3.63 mmol) and copper (I) iodide, and the mixture was stirred at room temperature for two hours. To the mixture was added ether, and the mixture was filtered through a cerite pad. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (2% methanol in chloroform) to give the title compound (1.05 g, 1.65 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05843957 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-2da4e8d7eb1e47438c125237e2b2157d |
| Source note | uspto-grants-1998_12 |