Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591841Generated: October 31, 2026

Butyl iodide → N-[4-(1-butyl-5-cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamide

https://huagongshe.com/reaction/1591841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantN-[4-(5-Cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamideHCID 16051191—
ReactantPotassium tert-butoxideHCID 23665647—
ProductN-[4-(1-butyl-5-cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamideHCID 1605127460.3%

Reaction Steps

N-[4-(5-cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamide (0.150 g, 0.54 mmol) was alkylated according to the procedure of Example 40 using potassium tert-butoxide (1.08 mL of a 1M solution, 1.08 mmol) and butyl iodide (0.066 mL, 0.50 mmol) to afford the title compound (0.10 g, 6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291643B2
Source datasetuspto-grants-2007_11
ORD IDord-e5573bb36a1341d8993543752c8fef78
Source noteuspto-grants-2007_11