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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | (1,1'-Biphenyl)-3,4-diamine | HCID 6452000 | — |
| Reactant | 1-Cyano-4-(tert-butylsulfonylamino)piperidine | HCID 23154173 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Tert-butylsulfonylaminopiperidin-1-yl)-5-phenylbenzimidazole | HCID 11373300 | 32.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691860B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-e65b0e739276460987c597aa6107c15b |
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| Source note | uspto-grants-2010_04 |
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