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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77504Generated: October 29, 2026

1-(1H-imidazole-1-carboximidoyl)-1H-imidazole → 5-{4-[3-tert-Butylsulfanyl-2-(2,2-dimethyl-propyl)-5-(pyridin-2-ylmethoxy)-indol-1-ylmethyl]-phenyl}-[1,3,4]oxadiazol-2-ylamine

https://huagongshe.com/reaction/77504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1H-imidazole-1-carboximidoyl)-1H-imidazoleHCID 11355654—
Reactant4-[3-tert-Butylsulfanyl-2-(2,2-dimethyl-propyl)-5-(pyridin-2-ylmethoxy)-indol-1-ylmethyl]-benzoic acid hydrazideHCID 66614581—
SolventDimethylformamideHCID 6228—
Product5-{4-[3-tert-Butylsulfanyl-2-(2,2-dimethyl-propyl)-5-(pyridin-2-ylmethoxy)-indol-1-ylmethyl]-phenyl}-[1,3,4]oxadiazol-2-ylamineHCID 66602303—

Reaction Conditions

Temperature85 °C

Reaction Steps

To 4-[3-tert-Butylsulfanyl-2-(2,2-dimethyl-propyl)-5-(pyridin-2-ylmethoxy)-indol-1-ylmethyl]-benzoic acid hydrazide (0.05 g, 0.10 mmol) in DMF (1 mL) was added C-(Di-imidazol-1-yl)-methyleneamine (0.08 g, 0.50 mmol), and the reaction was heated at 85° C. for 3 hours. The mixture was cooled to room temperature and partitioned between water and EtOAc. The aqueous layer was extracted with EtOAc, and the combined organic layers were dried over MgSO4, filtered, and concentrated. The residue was purified on silica gel (EtOAc:hexane gradient) to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841295B2
Source datasetuspto-grants-2014_09
ORD IDord-8115da312e604af0bbd6e69133dc17b4
Source noteuspto-grants-2014_09