HuagongsheHuagongshe Chemistry Print Report · For research reference only
Binap, (A+-)- → HCID 58576668, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 5-Bromo-2-nitropyridine | HCID 817620 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58576668 | HCID 58576668 | — |
Reaction Steps
A mixture of 4-amino-piperidine-1-carboxylic acid tert-butyl ester (500 mg; 2.5 mmol), 5-bromo-2-nitro-pyridine (406 mg; 2.0 mmol), Tris(dibenzylideneacetone)dipalladium (36 mg; 0.04 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (75 mg; 0.12 mmol), and sodium tert-butoxide (280 mg; 3.00 mmol) is suspended in toluene (5 mL) and is irradiated in a mono-mode microwave oven for 30 minutes at 120° C. The mixture is then concentrated under reduced pressure and the crude residue is purified by column chromatography on silica gel (dichloromethane:ethyl acetate 1:0 and then 4:1). The desired product is obtained with 78% purity (200 mg; 0.62 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096524B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-c935d191776c4524b4b371355078a5fa |
| Source note | uspto-grants-2015_08 |