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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461494Generated: October 31, 2026

1,2,3,4-Tetrahydroisoquinolin-8-amine → 8-Sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/461494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-Tetrahydroisoquinolin-8-amineHCID 20523209—
Reactant2-Acetyl-8-sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinolineHCID 21393832—
Product8-Sulfamoyl-7-trifluoromethyl-1,2,3,4-tetrahydroisoquinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04062961
Source datasetuspto-grants-1977_12
ORD IDord-23871e9f97a24f6e86d1f4dae4d9e2d8
Source noteuspto-grants-1977_12