HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 3-(Chloroacetyl)-1H-indole-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Indole-5-carbonitrile | HCID 27513 | — |
| Reactant | 5-Cyanotryptamine | HCID 58926 | — |
| Product | 3-(Chloroacetyl)-1H-indole-5-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532241 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-2342fa222038480ab253499ec9e85b6d |
| Source note | uspto-grants-1996_07 |