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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882899Generated: October 30, 2026

4-Chlorobenzenesulfonyl chloride → [4-(4-Chloro-benzenesulfonylamino)-butyl]-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromide

https://huagongshe.com/reaction/882899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
Reactant4-MethylmorpholineHCID 7972—
Reactant(4-Amino-butyl)-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromideHCID 86656640—
SolventDimethylformamideHCID 6228—
Product[4-(4-Chloro-benzenesulfonylamino)-butyl]-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromideHCID 57393279—

Reaction Steps

A solution of (4-amino-butyl)-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromide (Intermediate N) (0.25 g, 0.60 mmol), 4-chlorobenzenesulfonyl chloride (0.125 g, 0.59 mmol) and N-methylmorpholine (0.3 mL, 2.73 mmol) in DMF (5 mL) is shaken at RT for 16 h. The reaction mixture is concentrated in vacuo, and the residue is purified by chromatography (basic alumina, 0-15% methanol in DCM) to obtain the title compound. M+ 504.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236808B2
Source datasetuspto-grants-2012_08
ORD IDord-f230d376d1de4ef2bc9fb3883f209a65
Source noteuspto-grants-2012_08