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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079241Generated: October 31, 2026

Triethylamine → HCID 58010639, compound

https://huagongshe.com/reaction/2079241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
ReactantHCID 10654361HCID 10654361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58010639HCID 5801063933%

Reaction Steps

EDCI (3.6 g, 19 mmol) was added to a solution of (R)-3-(methoxycarbonyl)-2-hydroxypropanoic acid (2.8 g, 19 mmol) and HOBt (2.6 g, 19 mmol) in DMF (200 mL). After stirring this mixture for 5 min, benzyl piperazine-1-carboxylate (4.2 g, 3.6 mL, 19 mmol) and triethylamine (2.6 mL, 19 mmol) were added and stirred for 3 days at room temperature. The reaction mixture was poured into water and extracted with EtOAc. After washing the organic layers with brine and water, drying over Na2SO4 and concentrating, purification via silica gel chromatography using 0-10% MeOH/CH2Cl2 gave 4-((R)-2-hydroxy-3-methoxycarbonyl-propionyl)-piperazine-1-carboxylic acid benzyl ester as an oil (2.19 g, 33%). 1H NMR (400 MHz, CDCl3) δ 7.40-7.31 (m, 5H), 5.15 (s, 2H), 4.79-4.74 (m, 1H), 3.95 (d, J=8.0 Hz, 1H), 3.79-3.74 (m, 1H), 3.74 (s, 3H), 3.71-3.44 (m, 7H), 2.62 (d, J=5.8 Hz, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-651138203acc4e1e96eea5600e15dfec
Source noteuspto-grants-2011_04