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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882900Generated: October 31, 2026

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

https://huagongshe.com/reaction/882900

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant(4-Chlorophenyl)methanesulfonyl chlorideHCID 227304—
Reactant(2-Amino-ethyl)-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromideHCID 86656647—
SolventDimethylformamideHCID 6228—
Product[2-(4-Chloro-phenylmethanesulfonylamino)-ethyl]-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromideHCID 86656646—

Reaction Steps

A solution of (2-amino-ethyl)-{2-[(3,5-diamino-6-chloro-pyrazine-2-carbonyl)-amino]-ethyl}-dimethyl-ammonium bromide (Intermediate K) (0.3 g, 0.78 mmol), (4-chloro-phenyl)-methanesulfonyl chloride (0.18 g, 0.78 mmol) and N-methylmorpholine (0.35 mL, 3.18 mmol) in DMF (5 mL) is shaken at RT for 16 h. After this time the solvent is removed in vacuo and the residue is subjected to chromatography (basic alumina, 0-15% methanol in DCM) to yield the title compound. M+ 490.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236808B2
Source datasetuspto-grants-2012_08
ORD IDord-ede6fa6295394d45b054ef61111b69eb
Source noteuspto-grants-2012_08