HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283264Generated: October 27, 2026
4-Aminophenol → 4-({2-[2-(5-Nitrofuran-2-yl)ethenyl]quinazolin-4-yl}amino)phenol
https://huagongshe.com/reaction/1283264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-[2-(5-Nitro-2-furyl)vinyl]-4-chloroquinazoline | HCID 53634079 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-({2-[2-(5-Nitrofuran-2-yl)ethenyl]quinazolin-4-yl}amino)phenol | HCID 54073999 | 64.1% |
Reaction Steps
A 250 ml Erlenmeyer flash equipped with a magnetic stirrer and oil bath for heating was charged with 8.0 g (0.07 mole) of p-aminophenol and 25 ml of dimethylformamide. After the p-aminophenol was dissolved by stirring, 9.05 g (0.03 mole) of 2-[2-(5-nitro-2-furyl)vinyl]-4-chloroquinazoline (IV) was added. The reaction mixture was then heated at 70°C-90°C for 2 hours after which 60 ml of water was added and the solution after cooling was placed in a refrigerator for crystallization. After 3 days, the brown yellow solid was collected, washed first with water, then methanol and then dried to obtain 7.20 g of product melting at 250°-60°C with decomposition. Recrystallization from a 1:1 dimethylformamidemethanol mixture gave 6.5 g of orange crystals of the purified product which melted at 270°-2°C with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03974277 |
|---|
| Source dataset | uspto-grants-1976_08 |
|---|
| ORD ID | ord-67a87f34694f4c1f918e77bc635989bf |
|---|
| Source note | uspto-grants-1976_08 |
|---|