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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82894Generated: October 25, 2026

N-(1-benzyl-6-(2-(1-methyl-1H-imidazole-4-sulfonamido)ethoxy)-2,3-dihydro-1H-inden-2-yl)-3-chloro-2,2-dimethylpropanamide → N-(2-(3-benzyl-2-(3-chloro-2,2-dimethylpropylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

https://huagongshe.com/reaction/82894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-benzyl-6-(2-(1-methyl-1H-imidazole-4-sulfonamido)ethoxy)-2,3-dihydro-1H-inden-2-yl)-3-chloro-2,2-dimethylpropanamideHCID 66740419—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-(3-benzyl-2-(3-chloro-2,2-dimethylpropylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamideHCID 66741593—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of N-(1-benzyl-6-(2-(1-methyl-1H-imidazole-4-sulfonamido)ethoxy)-2,3-dihydro-1H-inden-2-yl)-3-chloro-2,2-dimethylpropanamide (51.8 mg, 0.095 mmol) in dry tetrahydrofuran (1 ml) was added 2M borane dimethyl complex (0.143 ml, 0.285 mmol) and stirred at 60° C. for 6 h and at room temperature over night. Quenched by dropwise addition of 0.5N hydrochloric acid and refluxed for an other 2 h, the solution was saponified with sodium hydroxide and extracted three times with dichloromethane, dried, filtered and evaporated to obtain the crude product (m=53 mg) as a yellow oil that was purified by flash silica gel chromatography on 4 g SiO2-cartridge using 5% methanol in dichloromethane to afford the titled compound N-(2-(3-benzyl-2-(3-chloro-2,2-dimethylpropylamino)-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide as a pale yellow oil. m=17.7 mg (35%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846743B2
Source datasetuspto-grants-2014_09
ORD IDord-143a082659a045ec979e52478a05df80
Source noteuspto-grants-2014_09