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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217389Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 178514883, compound

https://huagongshe.com/reaction/217389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86630442HCID 86630442—
SolventDimethylformamideHCID 6228—
ProductHCID 178514883HCID 17851488350%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a suspension of 4-hydroxy-1-(3-trifluoromethylphenyl)-3-(3-trifluoromethylphenylacetyl)-1,8-naphthyridin-2(1H)-one (740 mg, 1.5 mmol) produced in Synthesis Example 15 in DMF (5 mL) was added hydrazine monohydrate (purity of 80%, 291 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-trifluoromethylbenzyl)-5-(3-trifluoromethylphenyl)-1H-pyrazolo[4,3-c][1,8]naphthyridin-4(5H)-one (364 mg, yield 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-63e7912ebb11490fba288471629a27c3
Source noteuspto-grants-2012_06