HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetyl-7-chloro-8-sulfamyl-1,2,3,4-tetrahydroisoquinoline → 7-Chloro-8-sulfamoyl-1,2,3,4-tetrahydroisoquinoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetyl-7-chloro-8-sulfamyl-1,2,3,4-tetrahydroisoquinoline | HCID 21393800 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 7-Chloro-8-sulfamoyl-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 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 and 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062961 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-bdfe5464217b4137a86a885629f1b56c |
| Source note | uspto-grants-1977_12 |