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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178959Generated: October 27, 2026

3-phenyl-1H-pyrrolo[3,2-c]pyridine → N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[3,2-c]pyridine-1-sulfonyl)-benzamide

https://huagongshe.com/reaction/1178959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-phenyl-1H-pyrrolo[3,2-c]pyridineHCID 58975078—
Reactant4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chlorideHCID 58975125—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[3,2-c]pyridine-1-sulfonyl)-benzamideHCID 5897523179%

Reaction Steps

Add a 5 ml THF solution of 3-Phenyl-1H-pyrrolo[3,2-c]pyridine (500 mg, 2.57 mmol, 1 eq) to a 4 ml THF solution of KotBu (303 mg, 2.70 mmol, 1.05 eq) under N2 atmosphere. Stir reaction for 10 minutes and then add a 5 ml THF solution of 4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (844 mg, 2.57 mmol, 1 eq). Stir reaction for 16 hours, remove solvent on rotovap, and purify by silica gel chromatography to give N-(4-Fluoro-benzyl)-4-(3-phenyl-pyrrolo[3,2-c]pyridine-1-sulfonyl)-benzamide (982 mg, 79% yield). Mass Spectrum (m/e): 485.96 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276516B2
Source datasetuspto-grants-2007_10
ORD IDord-6852156c72714cedb8576b694088d6e5
Source noteuspto-grants-2007_10