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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397839Generated: October 30, 2026

Hydrochloric Acid → HCID 70829816, compound

https://huagongshe.com/reaction/1397839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant1H-Pyrrolo(2,3-b)pyridine-5-carbonitrileHCID 11788355—
ReactantN-(2,4-Difluoro-3-formylphenyl)-1-propanesulfonamideHCID 53419003—
SolventMethanolHCID 887—
ProductHCID 70829816HCID 7082981636.9%

Reaction Steps

1H-pyrrolo[2,3-b]pyridine-5-carbonitrile (13, 301 mg, 2.10 mmol), propane-1-sulfonic acid (2,4-difluoro-3-formyl-phenyl)-amide (12, 1.11 g, 4.20 mmol) and potassium hydroxide (354 mg, 6.31 mmol) were combined in a vial with 4.2 mL of methanol. The reaction was stirred for 3 hours at room temperature. The reaction solution was neutralized with 0.1 N aqueous hydrochloric acid and extracted 3× with ethyl acetate. The organic layers were combined and washed with brine, then dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. This was allowed to stir over the weekend at room temperature, then extracted with ethyl acetate and water. The organic layer was washed with brine and then dried over magnesium sulfate, filtered, and the solvents were removed from the filtrate under vacuum. The resulting material was purified by silica gel column chromatography eluting with ethyl acetate in hexanes to provide the desired compound (14, 315 mg). MS(ESI) [M−H+]−=405.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901301B2
Source datasetuspto-grants-2014_12
ORD IDord-9002dd4896b842699aefa2388b23a21a
Source noteuspto-grants-2014_12