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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639436Generated: October 31, 2026

Toluene → 2-(4-Tert-butylsulfonylaminopiperidin-1-yl)-5-phenylbenzimidazole

https://huagongshe.com/reaction/639436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantYtterbium triflateHCID 2733225—
Reactant(1,1'-Biphenyl)-3,4-diamineHCID 6452000—
Reactant1-Cyano-4-(tert-butylsulfonylamino)piperidineHCID 23154173—
SolventEthyl AcetateHCID 8857—
Product2-(4-Tert-butylsulfonylaminopiperidin-1-yl)-5-phenylbenzimidazoleHCID 1137330032.4%

Reaction Conditions

Temperature130 °C

Reaction Steps

To the toluene solution (1 mL) containing 1-cyano-4-(tert-butylsulfonylamino)piperidine (22 mg) were added 4-phenyl-1,2-phenylenediamine (20 mg) and ytterbium triflate (20 mg), and the mixture was stirred in a sealed tube at 130° C. for 16 hrs. The reaction mixture was cooled to room temperature and diluted with ethyl acetate. The organic layer was washed with aqueous saturated sodium hydrogencarbonate solution and aqueous saturated sodium chloride solutions successively, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was separated and purified on a collective thin-layer chromatograph (chloroform:methanol=15:1) to give the title compound (12 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691860B2
Source datasetuspto-grants-2010_04
ORD IDord-e65b0e739276460987c597aa6107c15b
Source noteuspto-grants-2010_04