HuagongsheHuagongshe Chemistry Print Report · For research reference only
56983-07-4 → HCID 22417875, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 56983-07-4 | HCID 4737324 | — |
| Reactant | 4-(Cyclohexylmethoxy)aniline | HCID 15681651 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22417875 | HCID 22417875 | 199.3% |
Reaction Steps
A solution of 1.0 g (4.5 mmol) of 4-chloro-2-methyl-8-nitroquinoline, 1.0 g (4.9 mmol) of 4-(cyclohexylmethyloxy)aniline and 30 mL of ethanol was heated under reflux for five hours. After cooling to room temperature, the reaction solution was evaporated to a residue which was slurried in in diethyl ether and filtered to furnish 2.0 g (99%) of N-[4-(cyclohexylmethyloxy)phenyl]-2-methyl-8-nitroquinolin-4-amine hydrochloride hydrate: m.p. 211°-214° C. (uncorr.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05506235 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-d6976401b0f84d73a1e2ee31b90f3fd2 |
| Source note | uspto-grants-1996_04 |