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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005887Generated: October 26, 2026

5-(4-Fluorophenyl)-2-piperazin-1-ylpyrimidine dihydrochloride → 1-{4-[5-(4-Fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/1005887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Fluorophenyl)-2-piperazin-1-ylpyrimidine dihydrochlorideHCID 22646672—
Reactant4-(R)-benzyl-3(2-(R)-{4-[5-(4-fluorophenyl)pyrimidin-2-yl)piperazine-1-sulfonylmethyl}-3-methylbutyryl)oxazolidin-2-oneHCID 23519754—
Reactant1-Chlorosulfonylmethylcyclohexanecarboxylic acid methyl esterHCID 58947956—
Product1-{4-[5-(4-Fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}cyclohexanecarboxylic acid methyl esterHCID 6989479548%

Reaction Steps

Prepared according to the method for the preparation of 4-(R)-benzyl-3-(2-(R)-{4-[5-(4-fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}-3-methyl-butyryl)oxazolidin-2-one, from 5-(4-fluorophenyl)-2-piperazin-1-ylpyrimidine, dihydrochloride (0.599 g) and 1-chlorosulfonylmethylcyclohexanecarboxylic acid methyl ester (0.575 g), to yield the title compound as a white solid (0.417 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787536B2
Source datasetuspto-grants-2004_09
ORD IDord-b54ffc7e9aef4b70b964fce8c597a5d1
Source noteuspto-grants-2004_09