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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501817Generated: November 4, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 86709514, compound

https://huagongshe.com/reaction/1501817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1-N-Boc-4-Piperidinecarboxylic acid methyl esterHCID 392870—
ReactantLithium diisopropylamideHCID 2724682—
Reactanttert-butyl N-((2S)-1-oxopropan-2-yl)carbamateHCID 7015728—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86709514HCID 86709514—

Reaction Steps

To a solution of LDA (prepared by adding n-BuLi (27.7 mL, 55.5 mmol) to diisopropylamine (8.04 mL, 57.3 mmol) in THF (40 mL) at 0° C., stir for 30 min) was added 1-tert-butyl 4-methyl piperidine-1,4-dicarboxylate (4500 mg, 18.5 mmol) in TMEDA (16.6 mL, 111 mmol) dropwise via syringe pump at −78° C. for 20 min. The mixture was stirred at the same temperature for 30 min, and (S)-tert-butyl (1-oxopropan-2-yl)carbamate (9931 mg, 57.3 mmol) in THF (20 mL) was added slowly by syringe pump for 20 min. The mixture was stirred at −78° C. for 30 min, and quenched with saturated NH4Cl at −78° C., warmed up to rt and diluted with EtOAc (200 mL). The organic layer was separated, and the aqueous layer was extracted with EtOAc (100 mL). The combined organic layers were washed with brine, dried (MgSO4), and concentrated. The residue was purified by column chromatography (MeOH/DCM, gradient 0-10%) to afford the title compound. LC/MS: [(M+1)]+=417

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206198B2
Source datasetuspto-grants-2015_12
ORD IDord-c6abe3063d2a4d3cbfdce25b9325357e
Source noteuspto-grants-2015_12