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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994665Generated: October 31, 2026

Ethanol → ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1994665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantethyl 1-(methoxymethyl)-7-nitro-1H-indole-2-carboxylateHCID 57475941—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Productethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylateHCID 5747594491.6%

Reaction Steps

A mixture of ethyl 1-(methoxymethyl)-7-nitro-1H-indole-2-carboxylate (2.35 g), 10% palladium-carbon (0.24 g), ethanol (4 ml) and tetrahydrofuran (10 ml) was stirred overnight at room temperature under hydrogen atmosphere. The palladium-carbon was removed by filtration, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give the title compound (1.92 g, yield 91%) as a yellow oil from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652133B2
Source datasetuspto-grants-2010_01
ORD IDord-67f97e2ab8f64f0b971032c5492c9dc2
Source noteuspto-grants-2010_01