HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole-5-carbonitrile → 3-(4-chlorobutanoyl)-1H-indole-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole-5-carbonitrile | HCID 27513 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | HCID 71714930 | HCID 71714930 | — |
| Product | 3-(4-chlorobutanoyl)-1H-indole-5-carbonitrile | HCID 10220528 | — |
Reaction Steps
In the second reaction line is schematically illustrated the synthesis of the intermediate 3-(4-chloro-1-hydroxy-butyl)-1H-indol-5-carbonitrile of Formula (I) through the condensing of indol-5-carbonitrile with 4-chlorobutyrylchloride to give 3-(4-chlorobutyryl)-1H-indol-5-carbonitrile, which is reduced with sodium borohydride, to give 3-(4-chloro-1-hydroxy-butyl)-1H-indol-5-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802851B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-6eb83bb228ab4d3d91d73de9d241ef49 |
| Source note | uspto-grants-2014_08 |