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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411559Generated: October 30, 2026

Potassium Carbonate → N-{3-[3-(4-Cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl)-N-methyl-1-butanesulfonamide

https://huagongshe.com/reaction/411559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Butanesulfonyl chlorideHCID 75430—
Reactant4-({3-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)benzonitrileHCID 18540886—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductN-{3-[3-(4-Cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl)-N-methyl-1-butanesulfonamideHCID 1854100935%

Reaction Steps

A solution of 1-butanesulfonyl chloride (39.1 mg, 0.25 mmol) in MeCN (2 mL) was added to a solution of 4-({3-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)benzonitrile (Preparation G; 74.6 mg, 0.25 mmol) in CHCl3 (0.5 mL). K2CO3 was added and the mixture was stirred at rt for 24 h. The mixture was filtered through a silica plug (500 mg), which plug was then eluted with MeCN:CHCl3 (80:20; 3×2.5 mL), followed by CHCl3:MeOH (95:5), to give the title compound in 35% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-2ccfe2348b2a4090aa8b01f471f3d953
Source noteuspto-grants-2003_05