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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035819Generated: November 1, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 66748454, compound

https://huagongshe.com/reaction/2035819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantSodium CarbonateHCID 10340—
ReactantTriisopropyl borateHCID 21531—
Reactant2-(Boc-amino)pyridineHCID 11206349—
Reactant1-(4-iodophenyl)pyrrolidineHCID 11277307—
ReactantButyllithiumHCID 178418339—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66748454HCID 667484549.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (1.6 M in hexane, 48.3 mL) was added dropwise to a solution of N,N,N′,N′-tetramethylethane-1,2-diamine (8.08 g) and tert-butyl pyridin-2-ylcarbamate (5.00 g) in THF (dry) (50 ml) at −78° C. The mixture was stirred at 0° C. under N2 for 2 hr. Triisopropyl borate (17.0 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 (11.7 g, wet). A mixture of the precipitate (349 mg), sodium carbonate (155 mg), tetrakis(triphenylphosphine)palladium(0) (42.3 mg) and 1-(4-iodophenyl)pyrrolidine (200 mg) in DME (25 mL) and water (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 (17.1 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575154B2
Source datasetuspto-grants-2013_11
ORD IDord-5e5c6c8067b24128a85c35aa0910b07f
Source noteuspto-grants-2013_11