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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694289Generated: November 2, 2026

4-Bromopyridinium chloride → HCID 59486385, compound

https://huagongshe.com/reaction/1694289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromopyridinium chlorideHCID 88100—
ReactantBinap, (A+-)-HCID 634876—
Reactanttert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 15296367—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 59486385HCID 5948638545%

Reaction Conditions

Temperature90 °C

Reaction Steps

Sodium tert-butylate (4 mmol) was added to a solution of 4-bromopyridine hydrochloride (1.9 mmol) in dry toluene (10 ml) under argon, followed by 3,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester (1.6 mmol) in toluene (5 ml). Argon was added to the mixture for 15 min, then (S)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.123 mmol) and tris(dibenzylidene acetone)dipalladium (0.041 mmol) were added. The mixture was heated at 90° C. for 4 h and the reaction progress was monitored by thin-layer chromatography. On completion of the reaction the mixture was diluted with ethyl acetate (100 ml) and extracted with water and saturated sodium chloride solution, dried (Na2SO4), filtered and concentrated to small volume. The crude product was purified by column chromatography (3% methanol in DCM). Yield: 45% 2. TFA (13 eq.) was added to a DCM solution (10 ml/mmol) of tert-butyl 9-(pyridin-4-yl)-3,9-diazaspiro[5.5]undecane-3-carboxylate (1 eq.) at 0° C. and the mixture was stirred for 2 h at RT. The solvent was removed and the product was dried under vacuum. The crude product was used in the following stage with no further purification. Yield: quantitative

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158628B2
Source datasetuspto-grants-2012_04
ORD IDord-64d8577c69b7424bad4c4365e0786957
Source noteuspto-grants-2012_04