HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Chlorophenyl)hydrazine → HCID 178434826, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Chlorophenyl)hydrazine | HCID 70624 | — |
| Reactant | Ethyl 6-benzyloxy-4-chloro-6-methyl-5,6,7,8-tetrahydroquinoline-3-carboxylate | HCID 21270424 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178434826 | HCID 178434826 | — |
Reaction Steps
A solution of ethyl 6-benzyloxy-4-chloro-6-methyl-5,6,7,8-tetrahydroquinoline-3-carboxylate (5.0 g) and p-chlorophenylhydrazine (2.0 g) in 75 mL of n-butanol is stirred at room temperature for 4 hours, then refluxed overnight. The reaction mixture is evaporated and the residue is treated with Et2O and 2N NaOH. The alkaline layer is separated, the pH is adjusted at 8 with dilute HCl, and the resulting precipitate is collected. This material is washed with EtH/Et2O and air-dried to obtain 8-benzyloxy-2-p-chlorophenyl-8-methyl-2,3,6,7,8,9-hexahydropyrazolo[4,3-c]quinolin-3(5H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04740512 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-328973a2399e4ce58ec76e3303e23bf8 |
| Source note | uspto-grants-1988_04 |