HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrazolo(5,1-a)isoquinoline, 5,6-dihydro-2-(3-methoxyphenyl)- → Pyrazolo(5,1-a)isoquinoline, 2-(m-methoxyphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrazolo(5,1-a)isoquinoline, 5,6-dihydro-2-(3-methoxyphenyl)- | HCID 3045616 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Pyrazolo(5,1-a)isoquinoline, 2-(m-methoxyphenyl)- | HCID 3045617 | — |
Reaction Steps
To a solution of 2.5 g. of 2-(m-methoxyphenyl)-5,6-dihydro-pyrazolo[5,1-a]isoquinoline in 100 ml. of benzene is gradually added with stirring 30 g. of MnO2 prepared as described by E. Pratt et al., J. Org. Chem. 26, 2973 (1961) and activated according to the procedure of J. M. Goldman, J. Org. Chem. 34, 1979 (1969). The obtained mixture is refluxed with stirring for five days, then filtered. The filtrate after evaporation and crystallization of the solid residue from isopropyl ether gives 1 g. of the title product, m.p. 109°-11° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075342 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-d765ab1f51f54d80a2975aae4695cbcd |
| Source note | uspto-grants-1978_02 |