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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288463Generated: October 25, 2026

2-Acetyl-7-chloro-8-sulfamyl-1,2,3,4-tetrahydroisoquinoline → 7-Chloro-8-sulfamoyl-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/reaction/1288463

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Acetyl-7-chloro-8-sulfamyl-1,2,3,4-tetrahydroisoquinolineHCID 21393800—
SolventHydrochloric AcidHCID 313—
Product7-Chloro-8-sulfamoyl-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 21393857—

Reaction Steps

2-Acetyl-7-chloro-8-sulfamyl-1,2,3,4-tetrahydroisoquinoline is hydrolyzed in refluxing 10% hydrochloric acid (60 ml.) for 2.5 hours. The reaction mixture is evaporated and the residue treated with methanol amd ether. The solid is filtered off to give 7-chloro-8-sulfamoyl-1,2,3,4-tetrahydroisoquinoline hydrochloride. The hydrochloride is treated with ammonium hydroxide as in Example 9 to give 7-chloro-8-sulfamoyl-1,2,3,4-tetrahydroisoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03988339
Source datasetuspto-grants-1976_10
ORD IDord-cf5e5a68ff594ce39b6b4a40285e3572
Source noteuspto-grants-1976_10