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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Fluoro-2-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-pyridine | HCID 117729627 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {2-[2-(Tetrahydro-pyran-2-yloxy)-ethoxy]-pyridin-4-yl}-hydrazine | HCID 117729647 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440974B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-9b75eef4e17740bfa0e7e9cea924f8d1 |
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| Source note | uspto-grants-2016_09 |
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