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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279308Generated: October 30, 2026

Ammonia → 1-(4-Chlorobenzyl)-4-[{(4-isopropylphenylsulfonyl)glycyl}aminomethyl]piperidine

https://huagongshe.com/reaction/279308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPiperidineHCID 8082—
ReactantSulfuryl chlorideHCID 24648—
Reactant4-(Propan-2-yl)benzene-1-sulfonyl chlorideHCID 2734882—
Reactant1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
SolventChloroformHCID 6212—
Product1-(4-Chlorobenzyl)-4-[{(4-isopropylphenylsulfonyl)glycyl}aminomethyl]piperidineHCID 18426209—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1-(4-chlorobenzyl)-4-((glycylamino)methyl}piperidine (14.8 mg, 0.05 mmol) in CHCl3 (2 mL) was treated with (piperidinomethyl)polystyrene resin (28 mg, 2.8 mmol/g), 4-isopropylbenzenesulfonyl chloride (1.5 equiv.) and stirred at 25° C. for 16 h. (Aminomethyl)polystyrene was added to scavenge the residual sulfonyl chloride and the reaction mixture was stirred at 25° C. for 16 h. Filtration and concentration afforded 1-(4-chlorobenzyl)-4-[{(4-isopropylphenylsulfonyl)glycyl}aminomethyl]piperidine (compound No. 869) (22.1 mg, 92%): The purity was determined by RPLC/MS (86%); ESI/MS m/e 478 (M++H, C24H32ClN3O3S).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-a0b05190b73c4376a5cc80334fe61dc3
Source noteuspto-grants-2002_03