Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aminoquinol | HCID 5708341 | — |
| Reactant | HCID 86600786 | HCID 86600786 | — |
| Product | HCID 18963800 | HCID 18963800 | — |
Reaction Steps
Appropriate 7-(pyridin-2-yl)-5,6,7,8-tetrahydro-N-(1,2,3,4-tetrahydro-4,4-dimethyl-1-substituted)quinolin-7-yl)pyrido[3,4-d]pyrimidin-4-amine derivatives are prepared starting from 1,2,3,4-tetrahydro-4,4-dimethyl-7-nitroquinoline. The nitroquinoline derivate is reacted with appropriate alkylating agent to give the N-substituted nitroquinoline, which is reduced using standard procedures known in the art to yield 7-aminoquinoline derivative. The resulting aminoquinoline derivated is then condensed with the appropriate 4-chloro-7-(pyridin-2-yl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine to give the desired 7-(pyridin-2-yl)-5,6,7,8-tetrahydro-N-(1,2,3,4-tetrahydro-4,4-dimethyl-1-substituted)quinolin-7-yl)pyrido[3,4-d]pyrimidin-4-amine derivative. As a representative example, preparation of the N-morpholionethyl derivative is depicted in Scheme 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07312330B2 |
|---|
| Source dataset | uspto-grants-2007_12 |
|---|
| ORD ID | ord-884e9ac9a6c74d5e86f9eb0f7ec6ed92 |
|---|
| Source note | uspto-grants-2007_12 |
|---|