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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217416Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 178514902, compound

https://huagongshe.com/reaction/217416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68948027HCID 68948027—
SolventDimethylformamideHCID 6228—
ProductHCID 178514902HCID 178514902—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a suspension of 4-hydroxy-3-(3-thienylacetyl)-1-(3-trifluoromethoxyphenyl)-1,8-naphthyridin-2(1H)-one (80 mg, 0.18 mmol) produced in Synthesis Example 42 in DMF (3 mL) was added hydrazine monohydrate (purity of 80%, 44 μL), and the mixture was stirred at 110 to 120° C. for 2 hours. To the reaction solution was added a sodium hydrogencarbonate aqueous solution. The resulting precipitate was separated by filtration, washed with water, recrystallized from methanol, and dried to give 3-(3-thienylmethyl)-5-(3-trifluoromethoxyphenyl)-1H-pyrazolo[4,3-c][1,8]-naphthyridin-4(5H)-one as a form of crystal (47 mg, yield 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-dc2ce551fc0444eb8bfea71864c71ffc
Source noteuspto-grants-2012_06