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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
ReactantHCID 178527435HCID 178527435—
SolventTolueneHCID 1140—
ProductHCID 178527374HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05173503
Source datasetuspto-grants-1992_12
ORD IDord-e66914a0cc934a02b3d0d63c60495bc4
Source noteuspto-grants-1992_12