HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (S)-2-(2-Pyridin-4-yl-ethyl)-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | (S)-1,4-dibenzyl-2-(2-pyridinyl-ethyl)-piperazine | HCID 17759583 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | (S)-2-(2-Pyridin-4-yl-ethyl)-piperazine | HCID 45115809 | 86% |
Reaction Steps
Dissolve (S)-1,4-dibenzyl-2-(2-pyridinyl-ethyl)-piperazine (2.14 g, 5.76 mmol) in ethanol (40 mL). Add ammonium formate (2.18 g, 34.6 mmol) and palladium (430 mg, 5 wt. % on carbon) and heat to reflux. After 6 hours 30 minutes, filter the palladium on carbon and concentrate the filtrate. Purify by silica gel chromatography using 7N ammonia in methanol-methylene chloride (5%–15%) as the eluent to give 945 mg (86%) of the title compound: mp 113–116° C.; mass spectrum (ion spray): m/z=192 (M+1). Analysis calculated for C11H17N3: C, 69.07; H, 8.96; N, 21.97. Found: C, 69.08; H, 8.77; N, 21.81.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214673B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-9278b8cc5ea34029aa6890f4327ea54c |
| Source note | uspto-grants-2007_05 |