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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625249Generated: October 29, 2026

2-Methoxyethylamine → (S)-N-(2-methoxyethyl)piperidine-3-carboxamide

https://huagongshe.com/reaction/625249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(3S)-1-((tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 6951168—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product(S)-N-(2-methoxyethyl)piperidine-3-carboxamideHCID 28162916100%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 0° C. solution of 500 mg of (S)-1-(tert-butoxycarbonyl)piperidine-3-carboxylic acid, 328 mg of 2-methoxyethylamine, 736 mg of HOBt, and 1.82 mL of triethylamine in 9 mL of dichloromethane was treated with 836 mg of EDC.HCl. The mixture was stirred at 25° C. overnight and the solvent was evaporated at reduced pressure. The residue was dissolved in ethyl acetate, and the solution was sequentially washed with water, an aqueous solution of citric acid, an aqueous sodium bicarbonate solution, and brine. The solution was dried (Na2SO4) and the solvent was evaporated. The residue was dissolved in a 4 M solution of HCl in dioxane. After 1 h the mixture was evaporated to give 406 mg of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301951B2
Source datasetuspto-grants-2016_04
ORD IDord-826cf19df4d14ff99e2ab61b5cfab288
Source noteuspto-grants-2016_04