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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432928Generated: November 1, 2026

Hydrochloric Acid → 2,6-Dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1432928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(2S,6RS)-4-[3-(Benzhydryl-amino)-4-cyano-benzyl]-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl esterHCID 57116643—
SolventEthyl AcetateHCID 8857—
Product2,6-Dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl esterHCID 54133253148.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(2S,6RS)-4-[3-(Benzhydryl-amino)-4-cyano-benzyl]-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester (2.6 g, 5.21 mmol) is dissolved in 100 mL of ethyl acetate and cooled to 0° C. A 12N solution of hydrochloric acid (0.5 ml, 6.0 mmol) is added dropwise. The deprotection is complete in thirty minutes. The reaction mixture is washed with 10% sodium bicarbonate. The ethyl acetate layer is dried with magnesium sulfate, filtered and condensed. The resulting residue is purified by flash colunm (SiO2, 60% ethyl acetate/hexane) to give the product (2S,6RS)-4-(3-amino)-4-cyano-benzyl)-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester (2.03 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-b115c984e55b431bbffdca08593d2f11
Source noteuspto-grants-2009_11