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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881743Generated: October 27, 2026

1,2-Dichloroethane → 5-isobutyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/881743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant3-MethylbutanehydrazideHCID 32283—
Reactant1,1'-Thiocarbonyldi-2(1H)-pyridoneHCID 853162—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
ReactantHCID 178418790HCID 178418790—
SolventDichloromethaneHCID 6344—
Product5-isobutyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,4-oxadiazol-2-amineHCID 8670084569%

Reaction Steps

To a stirred solution of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) aniline (200 mg, 0.91 mmol) in methylene chloride (4.5 ml) was added 1,1′-thiocarbonyldipyridin-2(1H)-one (212 mg, 0.91 mmol) and stirred at room temperature for 1 hour. Upon complete formation of the isothiocyanate, 3-methylbutanehydrazide (159 mg, 1.37 mmol) was added to the mixture and stirred at room temperature for overnight. EDC (315 mg, 1.64 mmol) was then added and the reaction stirred at room temperature for 14 hours. The reaction was concentrated to dryness and taken up in water to form a slurry. The slurry was filtered and washed with water to afford the crude product, which was purified by column chromatography to afford the title compound as off-white solid after drying (217 mg, 69% yield). LC/MS, ESI-MS(+) m/z 344.1, RT 1.45 (Condition R).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993619B2
Source datasetuspto-grants-2015_03
ORD IDord-ed005af77e91469691fd62a286bd34c3
Source noteuspto-grants-2015_03