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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23149Generated: October 25, 2026

Toluene → N-[2-(ethylamino)ethyl]-5-nitro-1H-indole-2-carboxamide

https://huagongshe.com/reaction/23149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiethyl EtherHCID 3283—
ReactantN-EthylethylenediamineHCID 66071—
ReactantEthyl 5-nitro-1H-indole-2-carboxylateHCID 280312—
SolventEthyl AcetateHCID 8857—
ProductN-[2-(ethylamino)ethyl]-5-nitro-1H-indole-2-carboxamideHCID 8580138082%

Reaction Steps

A fine powder of 5-nitro-2-indolecarboxylic acid ethyl ester (0.8 g, 3.41 mmol) was suspended in 2 ml of N-ethylethylenediamine under argon and the reaction mixture was stood at 55° C. overnight. The mixture was co-evaporated with toluene to dryness. The brown solid obtained was dissolved in 6 ml of ethyl acetate and 40 ml of ether was added to precipitate the product. After centrifugation, the liquid was poured out and the solid was washed with 30 ml of ether and dried to give small brown crystals (0.77 g, 82%). ESI MS: 277.11 (M+H+), 299.09 (M+Na+). 1H NMR (DMSO-d6) δ8.67 (d, 1H), 8.04 (dd, 1H), 7.55 (d, 1H), 7.37 (s), 3.36 (m, 3H), 2.69 (q, 2H), 2.55 (q, 2H), 0.99 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849713B2
Source datasetuspto-grants-2005_02
ORD IDord-40e663da5a7b4c6aa33aec3ec44db7c1
Source noteuspto-grants-2005_02