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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178985Generated: October 26, 2026

Potassium tert-butoxide → N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamide

https://huagongshe.com/reaction/1178985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-phenyl-1H-pyrrolo[2,3-b]pyridineHCID 52270684—
Reactant4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chlorideHCID 58975125—
SolventDimethylformamideHCID 6228—
ProductN-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamideHCID 5784904518.5%

Reaction Steps

Slowly add 3-phenyl-1H-pyrrolo[2,3-b]pyridine (178 mg, 0.915 mmol, 1.0 eq) as a 2 ml DMF solution to a flask under N2 containing potassium tertbutoxide (108 mg, 0.961 mmol, 1.05 eq) in 1 ml DMF solution. Stir solution for 5 minutes. Slowly add 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (300 mg, 0.915 mmol, 1.0 eq) as a 3 ml DMF solution. Stir reaction for 18 hours at room temperature. Strip reaction of solvent and purify on silica gel chromatography to give N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[2,3-b]pyridine-1-sulfonyl)-benzamide (82 mg, 18% yield). Mass Spectrum (m/e): 485.94 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276516B2
Source datasetuspto-grants-2007_10
ORD IDord-e82320606cbb4546ad773905ac96c429
Source noteuspto-grants-2007_10