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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352761Generated: November 1, 2026

Pentane → 1-tert-Butoxycarbonyl-4-[[(2RS)-2-(6-chloropyridin-3-yl)-2-hydroxyethyl]sulfonyl]piperazine

https://huagongshe.com/reaction/352761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
ReactantTert-butyl 4-(methylsulfonyl)piperazine-1-carboxylateHCID 4496004—
ReactantHCID 178418306HCID 178418306—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-tert-Butoxycarbonyl-4-[[(2RS)-2-(6-chloropyridin-3-yl)-2-hydroxyethyl]sulfonyl]piperazineHCID 22709547—

Reaction Steps

In tetrahydrofuran (8 ml), 1-tert-butoxycarbonyl-4-methanesulfonylpiperazine (838 mg) was dissolved, followed by the addition of tert-butyl lithium (a 1.7M pentane solution, 1.72 ml) at −78° C. in an argon gas atmosphere. The resulting mixture was stirred for 2 hours. After the dropwise addition of a solution of 6-chloronicotinaldehyde (346 mg) in tetrahydrofuran (tetrahydrofuran: 4 ml) and stirring at −78° C. for 3 hours, the reaction mixture was added with isopropanol (1 ml). The resulting mixture was heated to room temperature and diluted with ethyl acetate. The diluted solution was washed with water and saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was recrystallized from ethyl acetate, whereby the title compound (532 mg, 54%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-f2f77e49cd5141cb9f43132adf2a1e14
Source noteuspto-grants-2004_06