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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528732Generated: October 30, 2026

Diisopropylethylamine → 1-Boc-N-(2-propyn-1-yl)azetidine-3-carboxamide

https://huagongshe.com/reaction/528732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPropargylamineHCID 239041—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Boc-Azetidine-3-carboxylic acidHCID 2755981—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDichloromethaneHCID 6344—
Product1-Boc-N-(2-propyn-1-yl)azetidine-3-carboxamideHCID 86667172—

Reaction Steps

To 0.5 g (2.48 mmol) boc-azetidine-3-carboxylic acid in 5 mL DCM were added 0.52 g (2.73 mmol) 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 0.4 g (2.98 mmol) 1-hydroxybenzotriazole hydrate and 0.9 mL (5.47 mmol) DIPEA, and the reaction was stirred at room temperature for 30 minutes. 0.19 mL (2.73 mmol) propargylamine was added and the reaction was stirred for 16 hours at room temperature. 5 mL DCM was added and the mixture was washed with 10 mL aqueous HCl (1 M), then 10 mL aqueous NaHCO3 (1 M) and 10 mL brine. The organic layer was dried over Na2SO4. After filtration and evaporation of the solvent the product was purified by column chromatography (silica, heptane/EtOAc 7:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-35d3d9d9a17d41278b9cdac0bf2ed3e9
Source noteuspto-grants-2016_05