HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848504Generated: October 31, 2026
N,N,N',N'-Tetramethylethylenediamine → HCID 86709514, compound
https://huagongshe.com/reaction/1848504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 1-N-Boc-4-Piperidinecarboxylic acid methyl ester | HCID 392870 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | tert-butyl N-((2S)-1-oxopropan-2-yl)carbamate | HCID 7015728 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86709514 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08952166B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-c8f8145cedd848c980796b0485618e13 |
|---|
| Source note | uspto-grants-2015_02 |
|---|