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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883108Generated: October 29, 2026

4-Azidobutyrophenone → 2-(3-Azidopropyl)-5-(2,5-difluorophenyl)-2-phenyl-2,3-dihydro-1,3,4-thiadiazole

https://huagongshe.com/reaction/883108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AzidobutyrophenoneHCID 10877918—
ReactantBenzenecarbothioic acid, 2,5-difluoro-, hydrazideHCID 55279024—
CatalystAcetic AcidHCID 176—
SolventDichloromethane ethanolHCID 21584144—
Product2-(3-Azidopropyl)-5-(2,5-difluorophenyl)-2-phenyl-2,3-dihydro-1,3,4-thiadiazoleHCID 8660483154.7%

Reaction Steps

To a solution of 2,5-difluorobenzothiohydrazide (1.5 g, 7.97 mmol) in EtOH/dichloromethane (3:1, 16 mL) was added 4-azido-1-phenylbutan-1-one (1.36 g, 7.17 mmol). After stirring at room temperature for 16 hours, acetic acid (2 drops) was added and the mixture was stirred for another 16 hours. The reaction mixture was then concentrated under reduced pressure and chromatographed (9:1 hexanes/ethyl acetate) to provide the product (1.41 g, 41%) as a bright yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236825B2
Source datasetuspto-grants-2012_08
ORD IDord-ab83fae08e8d45afa88eb0c335d63300
Source noteuspto-grants-2012_08