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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339181Generated: October 26, 2026

C-(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methylamine → (6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

https://huagongshe.com/reaction/339181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC-(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methylamineHCID 11652370—
Reactant1H-Imidazole, 4,5-dihydro-2-(methylthio)-, hydriodide (1:1)HCID 12221228—
SolventDichloromethaneHCID 6344—
Product(6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amineHCID 1168921549.8%

Reaction Conditions

Temperature150 °C

Reaction Steps

C-(6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methylamine (100 mg, 0.31 mmol) and 2-methylsulfanyl-4,5-dihydro-1H-imidazole hydroiodide (76 mg, 0.31 mmol) were added to 2 mL CH2Cl2, and the reaction mixture was heated to gentle reflux until all of the solvent was evaporated. The reaction mixture was heated to 150° C. for 30 minutes and then cooled. The crude mixture was basified by dropwise addition of aqueous NaOH solution, and then purified by preparative liquid chromatography (CH2Cl2/MeOH 90:10) on a short silica gel column. Removal of the solvent afforded 57 mg (47%) of (6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine. MS: 370 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889906B2
Source datasetuspto-grants-2014_11
ORD IDord-30047680f4784c4a9401080e23349e9d
Source noteuspto-grants-2014_11