Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 22125028 | HCID 22125028 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 22124987 | HCID 22124987 | 100% |
Reaction Steps
A mixture of 1.1 g (1.5 mmol) of 1-[3-(2-(tert-butyldiphenylsilyloxy)ethyl)phenyl]-3-(2-chloro-6-methylphenyl)-3,4-dihydro-7-methanesulfonyl-pyrimido[4,5-d]pyrimidin-2(1H)-one and 3 ml of aniline was heated at 180° C. for 20 minutes. The mixture was cooled and added to 50 ml of 2M aqueous hydrochloric acid. The resulting suspension was filtered and the solid washed with water and dried to give 1.2 g (100%) of 1-[3-(2-(tert-butyldiphenylsilyloxy)ethyl)phenyl]-7-anilino-3-(2-chloro-6-methylphenyl)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one as a tan solid. [Mass spectrum (ESI) MH+ =724].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06150373 |
|---|
| Source dataset | uspto-grants-2000_11 |
|---|
| ORD ID | ord-b928aeee6f974474a18f548779634339 |
|---|
| Source note | uspto-grants-2000_11 |
|---|