HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyrrolidin-1-ylmethyl-piperidine → 1-(Indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyrrolidin-1-ylmethyl-piperidine | HCID 2760541 | — |
| Reactant | 1H-Indene-1-carbonyl chloride | HCID 18915077 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(Indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine | HCID 18915046 | 32.2% |
Reaction Steps
From 2.36 g of 2-(pyrrolidin-1-ylmethyl)piperidine. 2.5 g of indene-1-carbonyl chloride and 4.88 ml of triethylamine. 1.4 g of 1-(indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine was obtained using a procedure similar to that in Example 2. In a mixed solvent to methanol, water and ethanol (2:1:1), this compound was catalytically reduced with 10% palladium on carbon. After completion of the reduction, the catalyst was filtered off. After evaporation of the solvent, the residue was treated with a 4N 1,4-dioxane solution of hydrogen chloride to obtain 1.05 g of the title compound, melting at 218°-221° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05270327 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-6cd615d1c8364f64afd0f52b3b22aee5 |
| Source note | uspto-grants-1993_12 |