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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393214Generated: October 30, 2026

2-Chlorobenzenesulfonyl chloride → 2-Chloro-benzenesulfonic acid 7-{[1-(morpholine-4-carbonyl)-piperidin-4-yl]-propyl-amino}-5,6,7,8-tetrahydro-naphthalen-2-yl ester

https://huagongshe.com/reaction/393214

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantDiisopropylethylamineHCID 81531—
Reactant{4-[(7-Hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-piperidin-1-yl}-morpholin-4-yl-methanoneHCID 22649552—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-benzenesulfonic acid 7-{[1-(morpholine-4-carbonyl)-piperidin-4-yl]-propyl-amino}-5,6,7,8-tetrahydro-naphthalen-2-yl esterHCID 12135185—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of {4-[(7-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-piperidin-1-yl}-morpholin-4-yl-methanone (50 μmole in 420 μL DCM) was added 30 μL of DIEA followed by 220 μL of a 0.25M solution of 2-chlorobenzenesulfonyl chloride in THF. The solution was allowed to stir for 24 h at 25° C. under N2. Concentrated in vacuo. The final product was isolated by preparative RPHPLC (YMC Combiprep ODS-A column, 10-90% acetonitrile: water (0.1% TFA)) to afford 2-Chloro-benzenesulfonic acid 7-{[1-(morpholine4-carbonyl)-piperidin-4-yl]-propyl-amino}-5,6,7,8-tetrahydro-naphthalen-2-yl ester 40 (5.1 mg), [M+H]+=690.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806278B2
Source datasetuspto-grants-2004_10
ORD IDord-3a3f9b0807804c0caab93e561e7f0d32
Source noteuspto-grants-2004_10