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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393705Generated: October 25, 2026

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

https://huagongshe.com/reaction/393705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Fluorophenyl)-2-piperazin-1-ylpyrimidine dihydrochlorideHCID 22646672—
Reactant4-[4-(4-Bromophenyl)piperazine-1-sulfonylmethyl]tetrahydropyran-4-carboxylic acidHCID 22646679—
Reactant4-Chlorosulfonyl-methyltetrahydropyran-4-carboxylic acid methyl esterHCID 86590244—
Product4-{4-[5-(4-Fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}tetrahydropyran-4-carboxylic acidHCID 2264672381%

Reaction Steps

Prepared according to the method for the preparation of 4-[4-(4-bromophenyl) -piperazine-1-sulfonylmethyl]tetrahydropyran-4-carboxylic acid, from 5-(4-fluorophenyl)-2-piperazin-1-ylpyrimidine dihydrochloride (0.27 g), and 4-chlorosulfonyl -methyltetrahydropyran-4-carboxylic acid methyl ester (0.25 g), to yield the title compound as white solid (0.31 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809100B2
Source datasetuspto-grants-2004_10
ORD IDord-d882af0c80a94046b1d8fcfb888aff72
Source noteuspto-grants-2004_10