HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzonitrile → 7-Acetoxy-4-(4-cyanoanilino)-6,7-dihydro-5H-cyclopenta[d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | 4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl acetate | HCID 19968935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Acetoxy-4-(4-cyanoanilino)-6,7-dihydro-5H-cyclopenta[d]pyrimidine | HCID 13913226 | 55.2% |
Reaction Steps
39.3 g of 7-acetoxy-4-chloro-6,7-dihydro-5H-cyclopenta[d]pyrimidine [prepared as described in step (b) above] and 24 g of p-aminobenzonitrile were dissolved in 180 ml of ethanol, and the solution was heated under reflux for 1.5 hours. At the end of this time, the solvent was evaporated off under reduced pressure, and the resulting residue was washed with a 1:1 by volume mixture of ethanol and toluene, to give 30 g of the title compound as pale grayish crystals, melting at 215°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04749704 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-064491002d1040118ff9c94364c8cb47 |
| Source note | uspto-grants-1988_06 |