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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217403Generated: October 29, 2026

Hydrazine hydrate (1:1) → HCID 178514866, compound

https://huagongshe.com/reaction/217403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68950634HCID 68950634—
SolventDimethylformamideHCID 6228—
ProductHCID 178514866HCID 178514866—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a suspension of 3-(2-chlorophenylacetyl)-4-hydroxy-1-(3-trifluoromethoxyphenyl)-1,8-naphthyridine-2(1H)-one (622 mg, 1.3 mmol) produced in Synthesis Example 29 in DMF (6 mL) was added hydrazine monohydrate (purity of 80%, 210 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-chlorobenzyl)-5-(3-trifluoromethoxyphenyl)-1H-pyrazolo[4,3-c][1,8]-naphthyridin-4(5H)-one as a form of crystal (579 mg, yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-e9c8d95424b0449891a9292a6a42f4cf
Source noteuspto-grants-2012_06