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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292798Generated: October 30, 2026

2-ethyl-5-(4-hydrazino-4-oxobutoxy)-1-(phenylmethyl)-1H-indole-3-acetamide → 5-(4-amino-4-oxobutoxy)-2-ethyl-1-(phenylmethyl)-1H-indole-3-acetamide

https://huagongshe.com/reaction/2292798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ethyl-5-(4-hydrazino-4-oxobutoxy)-1-(phenylmethyl)-1H-indole-3-acetamideHCID 21191847—
ReactantEthylacetate methanolHCID 21584119—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product5-(4-amino-4-oxobutoxy)-2-ethyl-1-(phenylmethyl)-1H-indole-3-acetamideHCID 1555185947.4%

Reaction Steps

A mixture of 150 mg (0.37 mmol) of 2-ethyl-5-(4-hydrazino-4-oxobutoxy)-1-(phenylmethyl)-1H-indole-3-acetamide and 200 mg of Raney Ni in 15 mL of ethanol was heated to maintain reflux for 2 hours. After cooling, the EtOH was poured off and the Raney Ni washed twice with methylene chloride. The combined washes were filtered, concentrated at reduced pressure and the residue chromatographed on silica eluting with EtOAc, then 10% MeOH/EtOAc to give 69 mg (47% yield) of 5-(4-amino-4-oxobutoxy)-2-ethyl-1-(phenylmethyl)-1H-indole-3-acetamide, mp 176°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684034
Source datasetuspto-grants-1997_11
ORD IDord-2eae466b02434689ae4bc6a858806a0f
Source noteuspto-grants-1997_11