HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681667Generated: November 3, 2026
1,2,3,4-Tetrahydroisoquinoline → HCID 178527374, compound
https://huagongshe.com/reaction/1681667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | — |
| Reactant | HCID 178527435 | HCID 178527435 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178527374 | HCID 178527374 | — |
Reaction Steps
A solution of 1,2,3,4-tetrahydroisoquinoline (13.22 g) and imidazole-4-sulphonyl chloride (7.57 g) in toluene (70 ml) was stirred for 1 hour and then allowed to stand overnight. It was evaporated and the residue partitioned between diethyl ether and aqueous sodium hydroxide. The aqueous layer was clarified by ether extraction and then acidified with concentrated hydrochloric acid. The precipitate was collected, washed with water and dried to give crude 4-(1,2,3,4-tetrahydroisoquinolin-2-ylsulphonyl)-1H-imidazole. A solution of this product (9 g) in dimethylformamide was treated with sodium hydride (1.13 g of 80% in oil), followed by dimethylsulphamoyl chloride (5.4 g). The mixture was stirred for 1 hour and poured into water. The precipitate was collected and worked up to give the starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05173503 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-e66914a0cc934a02b3d0d63c60495bc4 |
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| Source note | uspto-grants-1992_12 |
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