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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217392Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 178514889, compound

https://huagongshe.com/reaction/217392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86630448HCID 86630448—
SolventDimethylformamideHCID 6228—
ProductHCID 178514889HCID 17851488951%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a suspension of 4-hydroxy-3-(3-trifluoromethoxyphenylacetyl)-1-(3-trifluoromethylphenyl)-1,8-naphthyridin-2(1H)-one (477 mg, 0.94 mmol) produced in Synthesis Example 18 in DMF (5 mL) was added hydrazine monohydrate (purity of 80%, 184 μL), and the mixture was stirred at 100 to 110° C. for 1 hour. To the reaction solution was added a sodium hydrogencarbonate aqueous solution. The resulting precipitate was separated by filtration, recrystallized from ethanol, and dried to give 3-(3-trifluoromethoxybenzyl)-5-(3-trifluoromethylphenyl)-1H-pyrazolo[4,3-c][1,8]naphthyridin-4(5H)-one (241 mg, yield 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-ced50c72930949baa2e7f27516a18545
Source noteuspto-grants-2012_06