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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693348Generated: October 31, 2026

Acetic Acid → 5-chloro-1H-pyrrolo(3,2-b)pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1693348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylateHCID 45480460—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product5-chloro-1H-pyrrolo(3,2-b)pyridine-2-carboxylic acidHCID 11665585—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylic acid ethyl ester (Preparation 5, 151 mg, 0.67 mmol) in ethanol (10 mL) was added sodium hydroxide (0.35 mL, 2M) and the stirred solution was heated at 70° C. for 2 h. The reaction mixture was then allowed to cool to rt and left to stand for 16 h. The pH was adjusted to 4 by addition of glacial acetic acid, the solvents removed in vacuo to give a white solid, which was suspended in dichloromethane and filtered through a sinter, washing with additional dichloromethane. The filter cake was washed with ethyl acetate (3×30 mL) and dried to give the title compound as a white solid. δH (CD3OD): 6.97 (1H, s), 7.17 (1H, d, 8.35 Hz), 7.83 (1H, d, 8.35 Hz); m/z (ES+)=197 [M+H]+; RT=2.82 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158622B2
Source datasetuspto-grants-2012_04
ORD IDord-39d8a9a7305749edb73c8027cb835fcd
Source noteuspto-grants-2012_04