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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292768Generated: October 30, 2026

HCID 10782159, compound → HCID 10732494, compound

https://huagongshe.com/reaction/2292768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10782159HCID 10782159—
ReactantEthylacetate methanolHCID 21584119—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 10732494HCID 1073249428%

Reaction Steps

A solution of 205 mg (0.634 mmol) of 2-methyl-5-nitro-1-(phenylmethyl)-1H-indole-3-acetamide in 30 mL of 2:1 THF/EtOH was hydrogenated at 60 psi (4218 g/cm2) of hydrogen for 4 hours using 0.1 g of Pd/C as catalyst. The catalyst was filtered and the filtrate concentrated at reduced pressure. The residue was chromatographed on silica eluting with EtOAc and then 5% MeOH/EtOAc to give 52 mg (28% yield) of 5-amino-2-methyl-1-(phenylmethyl)-1H-indole-3-acetamide, mp, 175°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684034
Source datasetuspto-grants-1997_11
ORD IDord-ab6b377f855e4e5bbb80fe0f0dd91b0f
Source noteuspto-grants-1997_11