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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626505Generated: October 27, 2026

Hydrazine hydrate (1:1) → N-(4-((6-aminopyridin-3-yl)oxy)pyridin-2-yl)cyclopropanecarboxamide

https://huagongshe.com/reaction/626505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-(4-((6-nitropyridin-3-yl)oxy)pyridin-2-yl)cyclopropanecarboxamideHCID 90410505—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductN-(4-((6-aminopyridin-3-yl)oxy)pyridin-2-yl)cyclopropanecarboxamideHCID 9040953187%

Reaction Steps

A solution of N-(4-((6-nitropyridin-3-yl)oxy)pyridin-2-yl)cyclopropanecarboxamide (1.50 g, 5.00 mmol) in MeOH (30 mL) was treated with hydrazine hydrate (1.50 g, 30.0 mmol) followed by Raney nickel (0.300 g, 5.11 mmol) and stirred at RT for 3 h. The solids were removed via filtration through diatomaceous earth, rinsed with DCM, then MeOH and the filtrate concentrated to dryness to afford N-(4-((6-aminopyridin-3-yl)oxy)pyridin-2-yl)cyclopropanecarboxamide (1.17 g, 87%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 11.21 (s, 1H), 8.56 (d, J=5.7 Hz, 1H), 8.19 (s, 1H), 8.01 (s, 1H), 7.68 (d, J=8.9 Hz, 1H), 7.06 (m, 1H), 6.92 (d, J=8.9 Hz, 1H), 6.43 (s, 2H), 2.37 (m, 1H), 1.18 (s, 4H); MS (ESI) m/z: 271.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309224B2
Source datasetuspto-grants-2016_04
ORD IDord-f0cbb2f269bd473abfe4debeb25ea922
Source noteuspto-grants-2016_04