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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60666Generated: October 27, 2026

Hydrazine hydrate (1:1) → {2-[2-(Tetrahydro-pyran-2-yloxy)-ethoxy]-pyridin-4-yl}-hydrazine

https://huagongshe.com/reaction/60666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4-Fluoro-2-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-pyridineHCID 117729627—
SolventEthanolHCID 702—
Product{2-[2-(Tetrahydro-pyran-2-yloxy)-ethoxy]-pyridin-4-yl}-hydrazineHCID 11772964789%

Reaction Conditions

Temperature80 °C

Reaction Steps

Intermediate 67a (633 mg, 2.62 mmol) was suspended in EtOH (5 mL) and hydrazine hydrate (50-60%, 5 mL) in a microwave vial fitted with a stirrer bar and sealed with a crimped septum, and heated to 80° C. for 18 h. The reaction was cooled, and partitioned between H2O and EtOAc. The organic layer was separated, and the aqueous extracted again with EtOAc. The combined organics were dried over MgSO4, and concentrated in vacuo to afford the title compound as a colorless oil (593 mg, 89%). LCMS (Method 3) Rt 0.41 and 1.71 min, m/z 276.2 [M+Na].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440974B2
Source datasetuspto-grants-2016_09
ORD IDord-9b75eef4e17740bfa0e7e9cea924f8d1
Source noteuspto-grants-2016_09