HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3,4-Tetrahydroisoquinoline → HCID 20556841, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178427692 | HCID 178427692 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 20556841 | HCID 20556841 | — |
Reaction Steps
To 3.46 g. of 3-phenyl-6-tosyloxymethyl-5,6-dihydro-4H-1,2,4-oxadiazine 1.33 g. of 1,2,3,4-tetrahydro-isoquinoline, 1.38 g. of anhydrous potassium carbonate and 30 ml. of chlorobenzene are added. The reaction mixture is refluxed for 2 hours, whereupon it is decolored and filtered while hot. Upon cooling 1.95 g. of 3-phenyl-6-(1,2,3,4-tetrahydro-2-isoquinolyl)-methyl-5,6-dihydro-4H-1,2,4-oxadiazine are obtained in crystalline form. The product has the same properties as the product of Example 4. Melting point: 187° to 189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04308270 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-9a955a4bd83b44efb897739ca24bd4f2 |
| Source note | uspto-grants-1981_12 |