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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278816Generated: November 2, 2026

Hydrazine hydrate (1:1) → 4-Chloro-6-methyl-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/2278816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2,4-Dichloro-6-methylnicotinaldehydeHCID 11252481—
Solvent1,2-DichloroethaneHCID 11—
Product4-Chloro-6-methyl-1H-pyrazolo[4,3-c]pyridineHCID 73012775—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2,4-dichloro-6-methylpyridine-3-carbaldehyde (12 g, 63 mmol) in 1,2-dichloroethane (200 mL) was added hydrazine monohydrate (9.52 g, 0.190 mol), and the reaction mixture was heated at 80° C. for 18 hours. After removal of solvents in vacuo, the residue was suspended in water (150 mL) and stirred for 30 minutes. The resulting precipitate was collected by filtration and washed with petroleum ether (2×250 mL), then was suspended in chloroform (150 mL), stirred for 30 minutes and filtered. The chloroform suspension was repeated twice to afford the product as a white solid. Yield: 6.7 g, 40 mmol, 63%. LCMS m/z 168.1 [M+H+]. 1H NMR (400 MHz, DMSO-d6) δ 13.70 (br s, 1H), 8.21 (s, 1H), 7.38 (s, 1H), 2.52 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133190B2
Source datasetuspto-grants-2015_09
ORD IDord-d8ea3bfbce64467b820ee7558a0f79e0
Source noteuspto-grants-2015_09