HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 9863633, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Isoquinolin-5-ol | HCID 30386 | — |
| Reactant | [(3,4-Dimethoxyphenyl)methylidene]propanedinitrile | HCID 219691 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 9863633 | HCID 9863633 | — |
Reaction Steps
To a stirred suspension of 5-hydroxyisoquinoline (2.90 g) and 3,4-dimethoxy benzylidenemalononitrile (4.28 g) in ethanol (11 ml) was added dropwise piperidine (1.70 g). The suspension was then heated at reflux temperature for one hour forming a red solution. This was then allowed to cool to room temperature, depositing a brown solid. This was filtered off and washed with ethanol and ether and dried in vacuo at 60° C., yielding 2-amino-4-(3,4-dimethoxyphenyl)- 4H-pyrano[2,3-f] isoquinoline-3-carbonitrile as a yellow-brown solid, m.p. 225°-228° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434160 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-049a88eba40a43aca12f9e9b6421a261 |
| Source note | uspto-grants-1995_07 |