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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032291Generated: October 30, 2026

6-fluoro-3-[4-(phenylmethyl)piperazinyl]-1H-indazole → 6-fluoro-3-piperazin-1-yl-1H-indazole

https://huagongshe.com/reaction/1032291

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-fluoro-3-[4-(phenylmethyl)piperazinyl]-1H-indazoleHCID 15057453—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-fluoro-3-piperazin-1-yl-1H-indazoleHCID 981587192%

Reaction Steps

A mixture of 12 parts of 6-fluoro-3-[4-(phenylmethyl)-piperazinyl]-1H-indazole, 1 part of Raney nickel catalyst and 200 parts of methanol was hydrogenated in a Parr-apparatus at normal pressure and at 50° C. with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off over diatomaceous earth and the filtrate was evaporated in vacuo. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 7.7 parts (92.0%) of 6-fluoro-3-(1-piperazinyl)-1H-indazole (int. 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957916
Source datasetuspto-grants-1990_09
ORD IDord-8c99c88cfcd643e9b610109696f0f84e
Source noteuspto-grants-1990_09