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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591843Generated: November 1, 2026

Propargyl bromide → HCID 16051276, compound

https://huagongshe.com/reaction/1591843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantN-[4-(5-Cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamideHCID 16051191—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 16051276HCID 160512766.3%

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 propargyl bromide (80% in toluene, 0.055 mL, 0.50 mmol) to afford the title compound (0.10 g, 6.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291643B2
Source datasetuspto-grants-2007_11
ORD IDord-29b23af0d1a541c6b46c4eb3d9c43bcd
Source noteuspto-grants-2007_11