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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071805Generated: October 27, 2026

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

https://huagongshe.com/reaction/1071805

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 numberUS06906103B2
Source datasetuspto-grants-2005_06
ORD IDord-38a46a1bea9d4e9b8074799be6b21537
Source noteuspto-grants-2005_06