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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (2S,6RS)-4-[3-(Benzhydryl-amino)-4-cyano-benzyl]-2,6-dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester | HCID 57116643 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,6-Dimethyl-3-oxo-piperazine-1-carboxylic acid benzyl ester | HCID 54133253 | 148.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-b115c984e55b431bbffdca08593d2f11 |
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| Source note | uspto-grants-2009_11 |
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