HuagongsheHuagongshe Chemistry Print Report · For research reference only
s-Triazolo(5,1-a)isoquinoline, 5,6-dihydro-2-phenyl- → s-Triazolo(5,1-a)isoquinoline, 2-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | s-Triazolo(5,1-a)isoquinoline, 5,6-dihydro-2-phenyl- | HCID 134397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | s-Triazolo(5,1-a)isoquinoline, 2-phenyl- | HCID 169678 | 56% |
Reaction Steps
Following substantially the same procedures of Example 58, and starting from 2-phenyl-5,6-dihydro-s-triazolo[5,1-a]isoquinoline, the title compound is prepared. Yield 56%, m.p. 157°-8° C (from ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075341 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-e5b40dc425814361a186da3a64f6d9fb |
| Source note | uspto-grants-1978_02 |