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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400956Generated: November 3, 2026

Ethyl Acetate → HCID 25418686, compound

https://huagongshe.com/reaction/1400956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantDichloromethane methanolHCID 21226129—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 25418686HCID 2541868634%

Reaction Conditions

Temperature62.5 °C

Reaction Steps

To a stirred solution of 1-Boc-piperazine (1.00 g, 5.37 mmol) and DIPEA (2.81 ml, 16.11 mmol) in DMSO (20 ml) under nitrogen at rt was added methyl (S)-(−)-3-bromo-2-methyl propionate (1.03 ml, 8.05 mmol), and the reaction mixture was heated at 60-65° C. over weekend. More methyl (S)-(−)-3-bromo-2-methyl propionate (1.03 ml, 8.05 mmol) was added, and the reaction mixture was heated at 65° C. overnight. The reaction mixture was diluted with AcOEt, and successively washed with water, a saturated aqueous solution of sodium bicarbonate and brine. The aqueous layers were combined, extracted with ethyl acetate, and successively washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by Biotage (Snap 25 g cartridge: MeOH/DCM: 0/100 to 5/95 over 20 CV, then 05/95 to 10/90 over 5 CV), to afford the desired product 565 (523 mg, 1.83 mmol, 34% yield) as a yellow oil. MS (m/z): 231.13 and 287.27 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-f5d46c0f89944c8fb34e21be6e57f63a
Source noteuspto-grants-2014_12