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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217396Generated: October 29, 2026

Hydrazine hydrate (1:1) → HCID 178514886, compound

https://huagongshe.com/reaction/217396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86630456HCID 86630456—
SolventDimethylformamideHCID 6228—
ProductHCID 178514886HCID 17851488632%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a suspension of 4-hydroxy-1-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylphenylacetyl)-1,8-naphthyridine-2(1H)-one (508 mg, 1.0 mmol) produced in Synthesis Example 22 in DMF (8 mL) was added hydrazine monohydrate (purity of 80%, 194 μL), and the mixture was stirred at 100 to 110° C. for 2 hours. 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 5-(3-trifluoromethoxyphenyl)-3-(4-trifluoromethylbenzyl)-1H-pyrazolo[4,3-c][1,8]naphthyridin-4(5H)-one (162 mg, yield 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-e5593f485f8f4f12b5fd928fa2f48c73
Source noteuspto-grants-2012_06