HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-indole-6-carbonitrile → HCID 15490886, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-indole-6-carbonitrile | HCID 85146 | — |
| Reactant | HCID 21201384 | HCID 21201384 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15490886 | HCID 15490886 | — |
Reaction Steps
77 mmol of potassium tert-butylate are added to a solution of 70 mmol of 6-cyanoindole in 400 ml of tetrahydrofuran. After 10 minutes' stirring at room temperature, 70 mmol of tert-butyl 3-[(methylphenyl)sulphonyloxymethyl]-1-pyrrolidinecarboxylate in 60 ml of tetrahydrofuran are added. The reaction mixture is heated at reflux for 12 hours. After cooling and dilution with water, the solvent is removed by evaporation. The residue is extracted with dichloromethane and the organic phase is washed with water, dried and concentrated to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06239129B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-d858b49666934ec78072c080364123e0 |
| Source note | uspto-grants-2001_05 |