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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883122Generated: October 30, 2026

Water → 1-(2-(3-azidopropyl)-5-(5-chloro-2-methylphenyl)-2-phenyl-1,3,4-oxadiazol-3(2H)-yl)-2,2-dimethylpropan-1-one

https://huagongshe.com/reaction/883122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPivaloyl chlorideHCID 62493—
ReactantN'-(4-azido-1-phenylbutylidene)-5-chloro-2-methyl benzohydrazideHCID 86604839—
SolventPyridineHCID 1049—
Product1-(2-(3-azidopropyl)-5-(5-chloro-2-methylphenyl)-2-phenyl-1,3,4-oxadiazol-3(2H)-yl)-2,2-dimethylpropan-1-oneHCID 8660484050.3%

Reaction Steps

To a solution of N′-(4-azido-1-phenylbutylidene)-5-chloro-2-methyl benzohydrazide (100 mg, 0.28 mmol) in pyridine (1 mL) was added pivaloyl chloride (70 μL, 0.56 mmol). After stirring at room temperature for 16 hours the heterogeneous mixture was treated with water (10 mL) and extracted with EtOAc (3×10 mL). The combined organic phases were washed successively with 10% NaHSO4 (2×10 mL), NaHCO3 (10 mL) and brine (10 mL) then dried over Na2SO4 and concentrated. The residue was purified by preparative TLC (9:1 hexanes/EtOAc) to afford the product (62 mg, 50%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236825B2
Source datasetuspto-grants-2012_08
ORD IDord-f0809a83739a492ba0641f94c82731d2
Source noteuspto-grants-2012_08