Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622849Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 86663616, compound

https://huagongshe.com/reaction/1622849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantPotassium CarbonateHCID 11430—
ReactantTriisopropyl borateHCID 21531—
Reactant2,5-DibromopyridineHCID 69353—
Reactant2-(Boc-amino)pyridineHCID 11206349—
ReactantButyllithiumHCID 178418339—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86663616HCID 8666361650%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (1.6 M in hexane, 48.3 mL) was added dropwise to a solution of N1,N1,N2,N2-tetramethylethane-1,2-diamine (8.08 g) and tert-butyl pyridin-2-ylcarbamate (5 g) in THF (dry) (50 mL) at −78° C. The mixture was stirred at 0° C. under N2 for 2 hr. Triisopropyl borate (16.95 g) was added to the mixture at −78° C. The mixture was stirred at 0° C. under N2 for 30 min. The mixture was quenched with sat. NH4Cl aq. at 0° C. and added with Et2O to give a yellow precipitate (11.68 g, wet). A mixture of potassium carbonate (438 mg), tetrakis(triphenylphosphine)palladium(0) (61.0 mg), 2,5-dibromopyridine (250 mg) and the precipitate (250 mg) in toluene (10 mL) and MeOH (5 mL) was stirred at 80° C. under N2 overnight. NH silica gel was added and the mixture was concentrated in vacuo. The residue was purified by column chromatography (NH silica gel, eluted with EtOAc in hexane) to give the title compound (132 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778934B2
Source datasetuspto-grants-2014_07
ORD IDord-26dd337791ba4373afb50a68882ec44e
Source noteuspto-grants-2014_07