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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217409Generated: October 29, 2026

Hydrazine hydrate (1:1) → HCID 178514865, compound

https://huagongshe.com/reaction/217409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68947293HCID 68947293—
SolventDimethylformamideHCID 6228—
ProductHCID 178514865HCID 178514865—

Reaction Conditions

Temperature115 °C

Reaction Steps

To a suspension of 3-(2-chlorophenylacetyl)-4-hydroxy-1-(3-trifluoromethylphenyl)-1,8-naphthyridin-2(1H)-one (687 mg, 1.5 mmol) produced in Synthesis Example 35 in DMF (6 mL) was added hydrazine monohydrate (purity of 80%, 240 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, and dried to give 3-(2-chlorobenzyl)-5-(3-trifluoromethylphenyl)-1H-pyrazolo[4,3-c][1,8]-naphthyridin-4(5H)-one as a form of crystal (632 mg, yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-495330d612e04c30bd5f75d7b13251ee
Source noteuspto-grants-2012_06