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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931579Generated: November 2, 2026

Water → HCID 57964979, compound

https://huagongshe.com/reaction/1931579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)cyclohexan-1-oneHCID 57964955—
SolventMethanolHCID 887—
ProductHCID 57964979HCID 5796497943%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-cyclohexanone (Intermediate 11; 600 mg, 2.9 mmol) and hydrazine hydrate (160 mg, 3.2 mmol) in methanol (2 mL) was heated at reflux for 3 h. The reaction mixture was cooled to 0° C. and sodium borohydride (220 mg, 5.8 mmol) was added portionwise. The reaction mixture was stirred at 0° C. for 4 h and then at room temperature overnight. Water was added and the aqueous layer was extracted three times with ethyl acetate. The combined organic layers were dried (sodium sulfate), filtered, and evaporated to give [4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-cyclohexyl]-hydrazine (280 mg, 43%) which was used directly in the next step without further purification. Mass spectrum M+=224.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188098B2
Source datasetuspto-grants-2012_05
ORD IDord-d534982253bc416bbdbdea12a5bd85f7
Source noteuspto-grants-2012_05