HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Piperidyl)pyridine → 1-Tert-butoxycarbonyl-4-[4-(4-pyridyl)-1-piperidylmethyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Piperidyl)pyridine | HCID 1139597 | — |
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | 1-Tert-butoxycarbonyl-4-[4-(4-pyridyl)-1-piperidylmethyl]piperidine | HCID 18328914 | 37.8% |
Reaction Steps
To a solution of 1-(tert-butoxycarbonyl)-4-(formyl)piperidine (2.59 g) and 4-(4-pyridyl)piperidine (1.97 g) in methanol/acetic acid (99:1) was added sodium cyanoborohydride (2.29 g) portionwise over 30 minutes and the resultant suspension stirred at ambient temperature for 3 hours. The suspension was quenched by addition of saturated aqueous sodium bicarbonate solution and the resulting mixture extracted with ethyl acetate. The organic phase was dried (Na2SO4) and evaporated. The residue was purified by chromatography eluting with 5% methanol in dichloromethane to give 1-tert-butoxycarbonyl-4-[4-(4-pyridyl)-1-piperidylmethyl]piperidine (1.65 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06335341B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-3eec01a6f9034ddb93efd3f1c4cc94b7 |
| Source note | uspto-grants-2002_01 |