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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377100Generated: November 1, 2026

Hydrochloric Acid → 4-Ethyl-1-(4-fluoro-benzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid hydroxyamide

https://huagongshe.com/reaction/2377100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydroxylamineHCID 787—
ReactantSodium HydroxideHCID 14798—
Reactant1h-Pyrrolo[2,3-c]pyridine-5-carboxylic acid,4-ethyl-1-[(4-fluorophenyl)methyl]-,ethyl esterHCID 59855822—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Ethyl-1-(4-fluoro-benzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid hydroxyamideHCID 11493352—

Reaction Steps

To a solution of 4-ethyl-1-(4-fluoro-benzyl)-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl ester (57 mg, 0.175 mmol) in EtOH (2 mL), was added a 10% wt/wt solution of NaOH in water (0.5 mL) and a 50% wt/wt solution of hydroxylamine in water (1 mL). The reaction was stirred at room temperature for 18 hours, and then 1 N HCl was added till a pH of 7 was reached. The reaction was concentrated by rotary evaporation, and then purified by preparative HPLC to give the desired product. Yield 10 mg, 18%. 1H NMR (400 MHz, CDCl3) δ 1.36 (t, J=7.58 Hz, 3H), 3.47 (q, J=7.41 Hz, 2H), 5.38 (s, 2H), 6375 (d, J=3.28 Hz, 1H), 7.02 (m, 2H), 7.13 (m, 2H), 7.30 (m, 1H), 8.43 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468375B2
Source datasetuspto-grants-2008_12
ORD IDord-88601713bd6a4d08a3209b90ad6b0f10
Source noteuspto-grants-2008_12