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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051013Generated: November 3, 2026

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

https://huagongshe.com/reaction/2051013

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 numberUS05015740
Source datasetuspto-grants-1991_05
ORD IDord-e917cc2fee1b4d01aa6d2c9be5496036
Source noteuspto-grants-1991_05