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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982503Generated: October 28, 2026

Ethyl (2R,3R)-3-{[(2S)-4-methyl-1-oxo-1-{4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl}pentan-2-yl]carbamoyl}oxirane-2-carboxylate → HCID 23700901, compound

https://huagongshe.com/reaction/1982503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (2R,3R)-3-{[(2S)-4-methyl-1-oxo-1-{4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl}pentan-2-yl]carbamoyl}oxirane-2-carboxylateHCID 6917749—
ReactantSodium hydroxide ethanolHCID 23692425—
SolventEthanolHCID 702—
ProductHCID 23700901HCID 2370090198%

Reaction Steps

Under cooling with ice, a 0.48N sodium hydroxide-ethanol solution (9.48 ml) was added to an ethanol solution (20 ml) of ethyl trans-3-[(s)-3-methyl-1-{4-(2,3,4-trimethoxyphenylmethyl)piperazine-1-yl carbonyl}butylcarbamoyl]-oxirane-2-carboxylate (2.38 g) obtained above, and the mixture was stirred at room temperature for 2.5 hours. After removal of ethanol by distillation under reduced pressure, water was added, and any insoluble matters were removed by filtration using sellaite. The filtrate was concentrated and dried under reduced pressure to yield 2.31 g of sodium trans-3-[(s)-3-methyl-1-{4-(2,3,4-trimethoxyphenylmethyl)piperazine-1-yl carbonyl}butylcarbamoyl]oxirane-2-carboxylate as a light yellow powder (yield: 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596803
Source datasetuspto-grants-1986_06
ORD IDord-6ad4ab21b0094001a3aa9d4576c6fd20
Source noteuspto-grants-1986_06