HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-4-phenylquinoline → Methyl 2,2-dimethyl-6-[(4-phenyl-2-quinolyl)amino]hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-4-phenylquinoline | HCID 2306687 | — |
| Reactant | Methyl 6-amino-2,2-dimethylhexanoate | HCID 15681405 | — |
| Product | Methyl 2,2-dimethyl-6-[(4-phenyl-2-quinolyl)amino]hexanoate | HCID 10474677 | — |
Reaction Steps
A mixture of 3.2 g of 2-chloro-4-phenyl-quinoline (prepared according to the method of S. Kwon and K. Isagawa, Yoki Gosei Kagaku Shi 1973,31, 313) and 5.9 g of methyl 6-amino-2,2-dimethylhexanoate is heated to 100 C. for 8 hours. After cooling, the residue is purified by chromatography on silica gel (eluent: 98:2 dichloromethane/methanol). to give methyl 2,2-dimethyl-6-[(4-phenyl-2-quinolyl)amino]hexanoate obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05492915 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-539ee989d1944f5f8e3f71b8dcbe5930 |
| Source note | uspto-grants-1996_02 |