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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733915Generated: November 1, 2026

Chloroacetyl chloride → 3-(Chloroacetyl)-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/1733915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantIndole-5-carbonitrileHCID 27513—
Reactant5-CyanotryptamineHCID 58926—
Product3-(Chloroacetyl)-1H-indole-5-carbonitrileHCID 15729288—

Reaction Steps

A mixture of 2.6 g of 3-(2-aminoethyl)-5-cyanoindole [obtainable by reaction of 5-cyanoindole with 2-chloroacetyl chloride to give 3-(2-chloroacetyl)-5-cyanoindole, subsequent reduction with diborane, reaction with phthalimide and hydrolysis]and one equivalent of 5-[N,N-bis(2-chloroethyl)amino]benzofuran [obtainable by reaction of 2-chloroacetyl chloride with 5-aminobenzofuran and subsequent reduction with diborane] in 40 ml of acetone and 40 ml of water is boiled for 20 hours and then worked up in the customary manner. 1-[2-(5-Cyanoindol-3-yl)ethyl]-4-(benzofuran-5-yl)piperazine is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532241
Source datasetuspto-grants-1996_07
ORD IDord-2342fa222038480ab253499ec9e85b6d
Source noteuspto-grants-1996_07