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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217405Generated: October 29, 2026

Hydrazine hydrate (1:1) → HCID 178514878, compound

https://huagongshe.com/reaction/217405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68949666HCID 68949666—
SolventDimethylformamideHCID 6228—
ProductHCID 178514878HCID 178514878—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a suspension of 4-hydroxy-3-(2-nitrophenylacetyl)-1-(3-trifluoromethoxyphenyl)-1,8-naphthyridin-2(1H)-one (450 mg, 0.93 mmol) produced in Synthesis Example 31 in DMF (4 mL) was added hydrazine monohydrate (purity of 80%, 148 μL), and the mixture was stirred at 110 to 120° C. for 3 hours. To the reaction solution was added a sodium hydrogencarbonate aqueous solution. The resulting precipitate was separated by filtration, washed with water, and dried to give 3-(2-nitrobenzyl)-5-(3-trifluoromethoxyphenyl)-1H-pyrazolo[4,3-c][1,8]-naphthyridin-4(5H)-one as a form of crystal (373 mg, yield 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-10600345f62945259d8d710de0a2a345
Source noteuspto-grants-2012_06