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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029737Generated: November 3, 2026

HCID 70147593, compound → HCID 70146441, compound

https://huagongshe.com/reaction/1029737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70147593HCID 70147593—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 70146441HCID 7014644141.1%

Reaction Steps

The benzyl group of 1-[(3-fluoro-4-pyridinyl)propylamino]-3-methyl-5-(phenylmethoxy)-1H-indole (15.82 g) was cleaved in a Parr hydrogenation apparatus in absolute ethanol (200 ml) over 10% Pd-C (1.58 g) at 50 psig and 50° C. for 7.5 hours. The catalyst was removed by filtration through a pad of celite and the solids washed with absolute ethanol. The combined filtrate was concentrated and the product purified via preparative HPLC (silica gel, 3:1 dichloromethane/EtOAc) affording 5.0 g of the desired product as an oil. Addition of EtOAc solidified the product which was recrystallized from EtOAc to give a solid, m.p. 157°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102891
Source datasetuspto-grants-1992_04
ORD IDord-2d818ae3965047c99780f4e2abbc8b17
Source noteuspto-grants-1992_04