HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3,4-Tetrahydroisoquinolin-8-amine → 8-Sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3,4-Tetrahydroisoquinolin-8-amine | HCID 20523209 | — |
| Reactant | 2-Acetyl-8-sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline | HCID 21393832 | — |
| Product | 8-Sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline | HCID 21393837 | — |
Reaction Steps
The above prepared 8-amino tetrahydroisoquinoline compound is converted to the corresponding 8-chlorosulfonyl compound and then to the 8-sulfamoyl compound, 2-acetyl-8-sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline, by the procedure of Example 15. The acetyl group is removed by acid hydrolysis by the procedure of Example 15 to give 8-sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062961 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-23871e9f97a24f6e86d1f4dae4d9e2d8 |
| Source note | uspto-grants-1977_12 |